{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,20]],"date-time":"2026-06-20T03:52:25Z","timestamp":1781927545273,"version":"3.54.5"},"reference-count":269,"publisher":"Japanese Society of Animal Reproduction","issue":"3","funder":[{"name":"JSPS KAKENHI","award":["22HP2009"],"award-info":[{"award-number":["22HP2009"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J. Reprod. Dev.","Journal of Reproduction and Development"],"published-print":{"date-parts":[[2026]]},"DOI":"10.1262\/jrd.2026-013","type":"journal-article","created":{"date-parts":[[2026,6,17]],"date-time":"2026-06-17T22:10:56Z","timestamp":1781734256000},"page":"239-255","source":"Crossref","is-referenced-by-count":0,"title":["Seminal fluid effects on female reproductive function in laboratory, livestock, and domestic species"],"prefix":"10.1262","volume":"72","author":[{"given":"Hon Yeung","family":"CHAN","sequence":"first","affiliation":[{"name":"School of Pharmacy and Biomedical Science and Robinson Research Institute, Adelaide University, SA 5005, Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"John E.","family":"SCHJENKEN","sequence":"additional","affiliation":[{"name":"Centre for Reproductive Science, School of Science, College of Engineering, Science and Environment, University of Newcastle, NSW 2308, Australia"},{"name":"Reproductive and Family Health Research Program, Hunter Medical Research Institute, NSW 2305, Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sarah A.","family":"ROBERTSON","sequence":"additional","affiliation":[{"name":"School of Pharmacy and Biomedical Science and Robinson Research Institute, Adelaide University, SA 5005, Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"349","reference":[{"key":"1","doi-asserted-by":"crossref","unstructured":"1. Schjenken JE, Robertson SA. The female response to seminal fluid. Physiol Rev<\/i> 2020; 100: 1077\u20131117.","DOI":"10.1152\/physrev.00013.2018"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Poiani A. Complexity of seminal fluid: a review. Behav Ecol Sociobiol<\/i> 2006; 60: 289\u2013310.","DOI":"10.1007\/s00265-006-0178-0"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Yamanaka T, Xiao Z, Tsujita N, Awad M, Umehara T, Shimada M. Testosterone-induced metabolic changes in seminal vesicle epithelium modify seminal plasma components with potential to improve sperm motility. eLife<\/i> 2025; 13: RP95541.","DOI":"10.7554\/eLife.95541.5"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Schjenken JE, Sharkey DJ, Green ES, Chan HY, Matias RA, Moldenhauer LM, Robertson SA. Sperm modulate uterine immune parameters relevant to embryo implantation and reproductive success in mice. Commun Biol<\/i> 2021; 4: 572.","DOI":"10.1038\/s42003-021-02038-9"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Akthar I, Kim Y, Umehara T, Kanno C, Sasaki M, Marey MA, Yousef MS, Haneda S, Shimada M, Miyamoto A. Activation of sperm Toll-like receptor 2 induces hyperactivation to enhance the penetration to mucus and uterine glands: a trigger for the uterine inflammatory cascade in cattle. Front Immunol<\/i> 2023; 14: 1319572.","DOI":"10.3389\/fimmu.2023.1319572"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Katila T. Post-mating inflammatory responses of the uterus. Reprod Domest Anim<\/i> 2012; 47(Suppl 5): 31\u201341.","DOI":"10.1111\/j.1439-0531.2012.02120.x"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Schjenken JE, Robertson SA. Seminal fluid and immune adaptation for pregnancy--comparative biology in mammalian species. Reprod Domest Anim<\/i> 2014; 49(Suppl 3): 27\u201336.","DOI":"10.1111\/rda.12383"},{"key":"8","unstructured":"8. McDonald LE, Black WG, McNutt SH, Casida LE. The response of the rabbit uterus to instillation of semen at different phases of the estrous cycle. Am J Vet Res<\/i> 1952; 13: 419\u2013424."},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Taylor NJ. Investigation of sperm-induced cervical leucocytosis by a double mating study in rabbits. J Reprod Fertil<\/i> 1982; 66: 157\u2013160.","DOI":"10.1530\/jrf.0.0660157"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Robertson SA. Seminal plasma and male factor signalling in the female reproductive tract. Cell Tissue Res<\/i> 2005; 322: 43\u201352.","DOI":"10.1007\/s00441-005-1127-3"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Thompson LA, Barratt CL, Bolton AE, Cooke ID. The leukocytic reaction of the human uterine cervix. Am J Reprod Immunol<\/i> 1992; 28: 85\u201389.","DOI":"10.1111\/j.1600-0897.1992.tb00765.x"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. De M, Choudhuri R, Wood GW. Determination of the number and distribution of macrophages, lymphocytes, and granulocytes in the mouse uterus from mating through implantation. J Leukoc Biol<\/i> 1991; 50: 252\u2013262.","DOI":"10.1002\/jlb.50.3.252"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Howe GR, Black DL. Spermatozoan transport and leucocytic responses in the reproductive tract of calves. J Reprod Fertil<\/i> 1963; 6: 305\u2013311.","DOI":"10.1530\/jrf.0.0060305"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Ribeiro AP, Vicente WR, Appar\u00edcio M, Gadelha CR, Alves AE, Covizzi GJ. Uterine leucocyte infiltration after artificial insemination in bitches. Theriogenology<\/i> 2006; 66: 1462\u20131464.","DOI":"10.1016\/j.theriogenology.2006.02.003"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. Katila T. Onset and duration of uterine inflammatory response of mares after insemination with fresh semen. Biol Reprod Mono<\/i> 1995; 1: 515\u2013517.","DOI":"10.1093\/biolreprod\/52.monograph_series1.515"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16. Phillips DM, Mahler S. Leukocyte emigration and migration in the vagina following mating in the rabbit. Anat Rec<\/i> 1977; 189: 45\u201359.","DOI":"10.1002\/ar.1091890104"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17. Mattner PE. Differential leucocytic responses to spermatozoa in the cervix and the uterus in ewes. J Reprod Fertil<\/i> 1969; 18: 297\u2013303.","DOI":"10.1530\/jrf.0.0180297"},{"key":"18","doi-asserted-by":"crossref","unstructured":"18. Rozeboom KJ, Troedsson MH, Crabo BG. Characterization of uterine leukocyte infiltration in gilts after artificial insemination. J Reprod Fertil<\/i> 1998; 114: 195\u2013199.","DOI":"10.1530\/jrf.0.1140195"},{"key":"19","doi-asserted-by":"crossref","unstructured":"19. Koedooder R, Mackens S, Budding A, Fares D, Blockeel C, Laven J, Schoenmakers S. Identification and evaluation of the microbiome in the female and male reproductive tracts. Hum Reprod Update<\/i> 2019; 25: 298\u2013325.","DOI":"10.1093\/humupd\/dmy048"},{"key":"20","doi-asserted-by":"crossref","unstructured":"20. Gopichandran N, Ekbote UV, Walker JJ, Brooke D, Orsi NM. Multiplex determination of murine seminal fluid cytokine profiles. Reproduction<\/i> 2006; 131: 613\u2013621.","DOI":"10.1530\/rep.1.00959"},{"key":"21","doi-asserted-by":"crossref","unstructured":"21. Narciandi F, Lloyd A, Meade KG, O\u2019Farrelly C. A novel subclass of bovine -defensins links reproduction and immunology. Reprod Fertil Dev<\/i> 2014; 26: 769\u2013777.","DOI":"10.1071\/RD13153"},{"key":"22","doi-asserted-by":"crossref","unstructured":"22. Alghamdi AS, Foster DN, Troedsson MH. Equine seminal plasma reduces sperm binding to polymorphonuclear neutrophils (PMNs) and improves the fertility of fresh semen inseminated into inflamed uteri. Reproduction<\/i> 2004; 127: 593\u2013600.","DOI":"10.1530\/rep.1.00096"},{"key":"23","doi-asserted-by":"crossref","unstructured":"23. Yanagimachi R, Chang MC. Infiltration of leucocytes into the uterine lumen of the golden hamster during the oestrous cycle and following mating. J Reprod Fertil<\/i> 1963; 5: 389\u2013396.","DOI":"10.1530\/jrf.0.0050389"},{"key":"24","doi-asserted-by":"crossref","unstructured":"24. Alghamdi AS, Lovaas BJ, Bird SL, Lamb GC, Rendahl AK, Taube PC, Foster DN. Species-specific interaction of seminal plasma on sperm-neutrophil binding. Anim Reprod Sci<\/i> 2009; 114: 331\u2013344.","DOI":"10.1016\/j.anireprosci.2008.10.015"},{"key":"25","doi-asserted-by":"crossref","unstructured":"25. Pini T, Leahy T, Paul de Graaf S. Seminal plasma and cryopreservation alter ram sperm surface carbohydrates and interactions with neutrophils. Reprod Fertil Dev<\/i> 2018; 30: 689\u2013702.","DOI":"10.1071\/RD17251"},{"key":"26","doi-asserted-by":"crossref","unstructured":"26. Tomlinson MJ, White A, Barratt CL, Bolton AE, Cooke ID. The removal of morphologically abnormal sperm forms by phagocytes: a positive role for seminal leukocytes? Hum Reprod<\/i> 1992; 7: 517\u2013522.","DOI":"10.1093\/oxfordjournals.humrep.a137682"},{"key":"27","doi-asserted-by":"crossref","unstructured":"27. Pandya IJ, Cohen J. The leukocytic reaction of the human uterine cervix to spermatozoa. Fertil Steril<\/i> 1985; 43: 417\u2013421.","DOI":"10.1016\/S0015-0282(16)48442-6"},{"key":"28","doi-asserted-by":"crossref","unstructured":"28. Alghamdi AS, Madill S, Foster DN, Troedsson MH. Equine sperm-neutrophil binding. Biol Reprod<\/i> 2015; 92: 94 (1-9).","DOI":"10.1095\/biolreprod.114.122655"},{"key":"29","doi-asserted-by":"crossref","unstructured":"29. Lessig J, Spalteholz H, Reibetanz U, Salavei P, Fischlechner M, Glander HJ, Arnhold J. Myeloperoxidase binds to non-vital spermatozoa on phosphatidylserine epitopes. Apoptosis<\/i> 2007; 12: 1803\u20131812.","DOI":"10.1007\/s10495-007-0113-5"},{"key":"30","doi-asserted-by":"crossref","unstructured":"30. Aitken RJ, Baker MA. Causes and consequences of apoptosis in spermatozoa; contributions to infertility and impacts on development. Int J Dev Biol<\/i> 2013; 57: 265\u2013272.","DOI":"10.1387\/ijdb.130146ja"},{"key":"31","doi-asserted-by":"crossref","unstructured":"31. Tecle E, Gagneux P. Sugar-coated sperm: Unraveling the functions of the mammalian sperm glycocalyx. Mol Reprod Dev<\/i> 2015; 82: 635\u2013650.","DOI":"10.1002\/mrd.22500"},{"key":"32","doi-asserted-by":"crossref","unstructured":"32. Doty A, Buhi WC, Benson S, Scoggin KE, Pozor M, Macpherson M, Mutz M, Troedsson MH. Equine CRISP3 modulates interaction between spermatozoa and polymorphonuclear neutrophils. Biol Reprod<\/i> 2011; 85: 157\u2013164.","DOI":"10.1095\/biolreprod.110.084491"},{"key":"33","doi-asserted-by":"crossref","unstructured":"33. Alghamdi AS, Foster DN. Seminal DNase frees spermatozoa entangled in neutrophil extracellular traps. Biol Reprod<\/i> 2005; 73: 1174\u20131181.","DOI":"10.1095\/biolreprod.105.045666"},{"key":"34","doi-asserted-by":"crossref","unstructured":"34. Rickard JP, Pini T, Soleilhavoup C, Cognie J, Bathgate R, Lynch GW, Evans G, Maxwell WM, Druart X, de Graaf SP. Seminal plasma aids the survival and cervical transit of epididymal ram spermatozoa. Reproduction<\/i> 2014; 148: 469\u2013478.","DOI":"10.1530\/REP-14-0285"},{"key":"35","doi-asserted-by":"crossref","unstructured":"35. Roldan ER, Gomendio M, Vitullo AD. The evolution of eutherian spermatozoa and underlying selective forces: female selection and sperm competition. Biol Rev Camb Philos Soc<\/i> 1992; 67: 551\u2013593.","DOI":"10.1111\/j.1469-185X.1992.tb01193.x"},{"key":"36","unstructured":"36. Krzymowski T, Stefa\u0144czyk-Krzymowska S, Koziorowski M. Counter current transfer of PGF2 alpha in the mesometrial vessels as a mechanism for prevention of luteal regression in early pregnancy. Acta Physiol Pol<\/i> 1989; 40: 23\u201334."},{"key":"37","doi-asserted-by":"crossref","unstructured":"37. Ratto MH, Leduc YA, Valderrama XP, van Straaten KE, Delbaere LT, Pierson RA, Adams GP. The nerve of ovulation-inducing factor in semen. Proc Natl Acad Sci USA<\/i> 2012; 109: 15042\u201315047.","DOI":"10.1073\/pnas.1206273109"},{"key":"38","doi-asserted-by":"crossref","unstructured":"38. Fernandez-Baca S, Madden DH, Novoa C. Effect of different mating stimuli on induction of ovulation in the alpaca. J Reprod Fertil<\/i> 1970; 22: 261\u2013267.","DOI":"10.1530\/jrf.0.0220261"},{"key":"39","doi-asserted-by":"crossref","unstructured":"39. Chen BX, Yuen ZX, Pan GW. Semen-induced ovulation in the bactrian camel (Camelus bactrianus). J Reprod Fertil<\/i> 1985; 74: 335\u2013339.","DOI":"10.1530\/jrf.0.0740335"},{"key":"40","doi-asserted-by":"crossref","unstructured":"40. Silva M, Ni\u00f1o A, Guerra M, Letelier C, Valderrama XP, Adams GP, Ratto MH. Is an ovulation-inducing factor (OIF) present in the seminal plasma of rabbits? Anim Reprod Sci<\/i> 2011; 127: 213\u2013221.","DOI":"10.1016\/j.anireprosci.2011.08.004"},{"key":"41","doi-asserted-by":"crossref","unstructured":"41. Waberski D, Claassen R, Hahn T, Jungblut PW, Parvizi N, Kallweit E, Weitze KF. LH profile and advancement of ovulation after transcervical infusion of seminal plasma at different stages of oestrus in gilts. J Reprod Fertil<\/i> 1997; 109: 29\u201334.","DOI":"10.1530\/jrf.0.1090029"},{"key":"42","doi-asserted-by":"crossref","unstructured":"42. O\u2019Leary S, Jasper MJ, Robertson SA, Armstrong DT. Seminal plasma regulates ovarian progesterone production, leukocyte recruitment and follicular cell responses in the pig. Reproduction<\/i> 2006; 132: 147\u2013158.","DOI":"10.1530\/rep.1.01119"},{"key":"43","doi-asserted-by":"crossref","unstructured":"43. Bogle OA, Ratto MH, Adams GP. Evidence for the conservation of biological activity of ovulation-inducing factor in seminal plasma. Reproduction<\/i> 2011; 142: 277\u2013283.","DOI":"10.1530\/REP-11-0042"},{"key":"44","doi-asserted-by":"crossref","unstructured":"44. Ratto MH, Huanca W, Singh J, Adams GP. Comparison of the effect of ovulation-inducing factor (OIF) in the seminal plasma of llamas, alpacas, and bulls. Theriogenology<\/i> 2006; 66: 1102\u20131106.","DOI":"10.1016\/j.theriogenology.2006.02.050"},{"key":"45","doi-asserted-by":"crossref","unstructured":"45. Kane MT, Morgan PM, Coonan C. Peptide growth factors and preimplantation development. Hum Reprod Update<\/i> 1997; 3: 137\u2013157.","DOI":"10.1093\/humupd\/3.2.137"},{"key":"46","doi-asserted-by":"crossref","unstructured":"46. Hardy K, Spanos S. Growth factor expression and function in the human and mouse preimplantation embryo. J Endocrinol<\/i> 2002; 172: 221\u2013236.","DOI":"10.1677\/joe.0.1720221"},{"key":"47","doi-asserted-by":"crossref","unstructured":"47. Robertson SA, Seamark RF, Guilbert LJ, Wegmann TG. The role of cytokines in gestation. Crit Rev Immunol<\/i> 1994; 14: 239\u2013292.","DOI":"10.1615\/CritRevImmunol.v14.i3-4.30"},{"key":"48","doi-asserted-by":"crossref","unstructured":"48. Sharkey AM, Dellow K, Blayney M, Macnamee M, Charnock-Jones S, Smith SK. Stage-specific expression of cytokine and receptor messenger ribonucleic acids in human preimplantation embryos. Biol Reprod<\/i> 1995; 53: 974\u2013981.","DOI":"10.1095\/biolreprod53.4.974"},{"key":"49","doi-asserted-by":"crossref","unstructured":"49. Robertson SA, Chin PY, Femia JG, Brown HM. Embryotoxic cytokines-Potential roles in embryo loss and fetal programming. J Reprod Immunol<\/i> 2018; 125: 80\u201388.","DOI":"10.1016\/j.jri.2017.12.003"},{"key":"50","doi-asserted-by":"crossref","unstructured":"50. Bromfield JJ, Schjenken JE, Chin PY, Care AS, Jasper MJ, Robertson SA. Maternal tract factors contribute to paternal seminal fluid impact on metabolic phenotype in offspring. Proc Natl Acad Sci USA<\/i> 2014; 111: 2200\u20132205.","DOI":"10.1073\/pnas.1305609111"},{"key":"51","doi-asserted-by":"crossref","unstructured":"51. Trowsdale J, Betz AG. Mother\u2019s little helpers: mechanisms of maternal-fetal tolerance. Nat Immunol<\/i> 2006; 7: 241\u2013246.","DOI":"10.1038\/ni1317"},{"key":"52","doi-asserted-by":"crossref","unstructured":"52. Robertson SA, Moldenhauer LM. Immunological determinants of implantation success. Int J Dev Biol<\/i> 2014; 58: 205\u2013217.","DOI":"10.1387\/ijdb.140096sr"},{"key":"53","doi-asserted-by":"crossref","unstructured":"53. Crawford G, Ray A, Gudi A, Shah A, Homburg R. The role of seminal plasma for improved outcomes during in vitro fertilization treatment: review of the literature and meta-analysis. Hum Reprod Update<\/i> 2015; 21: 275\u2013284.","DOI":"10.1093\/humupd\/dmu052"},{"key":"54","doi-asserted-by":"crossref","unstructured":"54. Robertson SA, Care AS, Moldenhauer LM. Regulatory T cells in embryo implantation and the immune response to pregnancy. J Clin Invest<\/i> 2018; 128: 4224\u20134235.","DOI":"10.1172\/JCI122182"},{"key":"55","doi-asserted-by":"crossref","unstructured":"55. Sharkey DJ, Tremellen KP, Jasper MJ, Gemzell-Danielsson K, Robertson SA. Seminal fluid induces leukocyte recruitment and cytokine and chemokine mRNA expression in the human cervix after coitus. J Immunol<\/i> 2012; 188: 2445\u20132454.","DOI":"10.4049\/jimmunol.1102736"},{"key":"56","doi-asserted-by":"crossref","unstructured":"56. Robertson SA, Sharkey DJ. Seminal fluid and fertility in women. Fertil Steril<\/i> 2016; 106: 511\u2013519.","DOI":"10.1016\/j.fertnstert.2016.07.1101"},{"key":"57","unstructured":"57. Robertson SA, Sharkey DJ. Seminal fluid cytokines in reproductive health and fertility of men. Fertil Steril<\/i> 2026; S0015-0282(26)00170-6."},{"key":"58","doi-asserted-by":"crossref","unstructured":"58. Parrilla I, Gil MA, Cuello C, Cambra JM, Gonzalez-Plaza A, Lucas X, Vazquez JL, Vazquez JM, Rodriguez-Martinez H, Martinez EA. Immunological uterine response to pig embryos before and during implantation. Reprod Domest Anim<\/i> 2022; 57(Suppl 5): 4\u201313.","DOI":"10.1111\/rda.14142"},{"key":"59","doi-asserted-by":"crossref","unstructured":"59. Campanile G, Baruselli PS, Limone A, D\u2019Occhio MJ. Local action of cytokines and immune cells in communication between the conceptus and uterus during the critical period of early embryo development, attachment and implantation - Implications for embryo survival in cattle: A review. Theriogenology<\/i> 2021; 167: 1\u201312.","DOI":"10.1016\/j.theriogenology.2021.02.020"},{"key":"60","doi-asserted-by":"crossref","unstructured":"60. Chu T, Jin Y, Wu G, Liu J, Sun S, Song Y, Zhang G. Insights into the single-cell transcriptome characteristics of porcine endometrium with embryo loss. FASEB J<\/i> 2025; 39: e70395.","DOI":"10.1096\/fj.202402212RR"},{"key":"61","doi-asserted-by":"crossref","unstructured":"61. Rudensky AY. Regulatory T cells and Foxp3. Immunol Rev<\/i> 2011; 241: 260\u2013268.","DOI":"10.1111\/j.1600-065X.2011.01018.x"},{"key":"62","doi-asserted-by":"crossref","unstructured":"62. Sakaguchi S. Regulatory T cells: key controllers of immunologic self-tolerance. Cell<\/i> 2000; 101: 455\u2013458.","DOI":"10.1016\/S0092-8674(00)80856-9"},{"key":"63","doi-asserted-by":"crossref","unstructured":"63. Shevach EM. CD4+ CD25+ suppressor T cells: more questions than answers. Nat Rev Immunol<\/i> 2002; 2: 389\u2013400.","DOI":"10.1038\/nri821"},{"key":"64","doi-asserted-by":"crossref","unstructured":"64. Madeja Z, Yadi H, Apps R, Boulenouar S, Roper SJ, Gardner L, Moffett A, Colucci F, Hemberger M. Paternal MHC expression on mouse trophoblast affects uterine vascularization and fetal growth. Proc Natl Acad Sci USA<\/i> 2011; 108: 4012\u20134017.","DOI":"10.1073\/pnas.1005342108"},{"key":"65","doi-asserted-by":"crossref","unstructured":"65. Hosking SL, Moldenhauer LM, Tran HM, Chan HY, Groome HM, Lovell EA, Green ES, O\u2019Hara SE, Roberts CT, Foyle KL, Davidge ST, Robertson SA, Care AS. Treg cells promote decidual vascular remodeling and modulate uterine NK cells in pregnant mice. JCI Insight<\/i> 2024; 10: 10.","DOI":"10.1172\/jci.insight.169836"},{"key":"66","doi-asserted-by":"crossref","unstructured":"66. Jalali BM, Kitewska A, Wasielak M, Bodek G, Bogacki M. Effects of seminal plasma and the presence of a conceptus on regulation of lymphocyte-cytokine network in porcine endometrium. Mol Reprod Dev<\/i> 2014; 81: 270\u2013281.","DOI":"10.1002\/mrd.22297"},{"key":"67","doi-asserted-by":"crossref","unstructured":"67. Cambra JM, Martinez-Serrano CA, Rodriguez-Martinez H, Vazquez JM, Cuello C, Gil MA, Martinez EA, Parrilla I. Deciphering immune tolerance in allogeneic pig pregnancy. Theriogenology<\/i> 2025; 238: 117363.","DOI":"10.1016\/j.theriogenology.2025.117363"},{"key":"68","doi-asserted-by":"crossref","unstructured":"68. Shima T, Inada K, Nakashima A, Ushijima A, Ito M, Yoshino O, Saito S. Paternal antigen-specific proliferating regulatory T cells are increased in uterine-draining lymph nodes just before implantation and in pregnant uterus just after implantation by seminal plasma-priming in allogeneic mouse pregnancy. J Reprod Immunol<\/i> 2015; 108: 72\u201382.","DOI":"10.1016\/j.jri.2015.02.005"},{"key":"69","doi-asserted-by":"crossref","unstructured":"69. Robertson SA, Guerin LR, Bromfield JJ, Branson KM, Ahlstr\u00f6m AC, Care AS. Seminal fluid drives expansion of the CD4+CD25+ T regulatory cell pool and induces tolerance to paternal alloantigens in mice. Biol Reprod<\/i> 2009; 80: 1036\u20131045.","DOI":"10.1095\/biolreprod.108.074658"},{"key":"70","doi-asserted-by":"crossref","unstructured":"70. Guerin LR, Moldenhauer LM, Prins JR, Bromfield JJ, Hayball JD, Robertson SA. Seminal fluid regulates accumulation of FOXP3+ regulatory T cells in the preimplantation mouse uterus through expanding the FOXP3+ cell pool and CCL19-mediated recruitment. Biol Reprod<\/i> 2011; 85: 397\u2013408.","DOI":"10.1095\/biolreprod.110.088591"},{"key":"71","doi-asserted-by":"crossref","unstructured":"71. Moldenhauer LM, Diener KR, Thring DM, Brown MP, Hayball JD, Robertson SA. Cross-presentation of male seminal fluid antigens elicits T cell activation to initiate the female immune response to pregnancy. J Immunol<\/i> 2009; 182: 8080\u20138093.","DOI":"10.4049\/jimmunol.0804018"},{"key":"72","doi-asserted-by":"crossref","unstructured":"72. Shima T, Nakashima A, Yasuda I, Ushijima A, Inada K, Tsuda S, Yoshino O, Tomura M, Saito S. Uterine CD11c+ cells induce the development of paternal antigen-specific Tregs via seminal plasma priming. J Reprod Immunol<\/i> 2020; 141: 103165.","DOI":"10.1016\/j.jri.2020.103165"},{"key":"73","doi-asserted-by":"crossref","unstructured":"73. Tamessar CT, Parameswaran S, Torres-Arce E, Weidenhofer J, Zhang HM, Mulhall JE, Robertson SA, Bromfield EG, Nixon B, Sharkey DJ, Skerrett-Byrne DA, Schjenken JE. Advancing Understanding of the Protein Composition of Human Seminal Extracellular Vesicles. Proteomics<\/i> 2026; 26: 178\u2013188.","DOI":"10.1002\/pmic.70088"},{"key":"74","doi-asserted-by":"crossref","unstructured":"74. Robertson SA, Mau VJ, Tremellen KP, Seamark RF. Role of high molecular weight seminal vesicle proteins in eliciting the uterine inflammatory response to semen in mice. J Reprod Fertil<\/i> 1996; 107: 265\u2013277.","DOI":"10.1530\/jrf.0.1070265"},{"key":"75","doi-asserted-by":"crossref","unstructured":"75. Tamessar CT, Trigg NA, Nixon B, Skerrett-Byrne DA, Sharkey DJ, Robertson SA, Bromfield EG, Schjenken JE. Roles of male reproductive tract extracellular vesicles in reproduction. Am J Reprod Immunol<\/i> 2021; 85: e13338.","DOI":"10.1111\/aji.13338"},{"key":"76","doi-asserted-by":"crossref","unstructured":"76. Samanta L, Parida R, Dias TR, Agarwal A. The enigmatic seminal plasma: a proteomics insight from ejaculation to fertilization. Reprod Biol Endocrinol<\/i> 2018; 16: 41.","DOI":"10.1186\/s12958-018-0358-6"},{"key":"77","doi-asserted-by":"crossref","unstructured":"77. Rodriguez-Martinez H, Martinez EA, Calvete JJ, Pe\u00f1a Vega FJ, Roca J. Seminal plasma: Relevant for fertility? Int J Mol Sci<\/i> 2021; 22: 4368.","DOI":"10.3390\/ijms22094368"},{"key":"78","doi-asserted-by":"crossref","unstructured":"78. Chu TM, Nocera MA, Flanders KC, Kawinski E. Localization of seminal plasma transforming growth factor-beta1 on human spermatozoa: an immunocytochemical study. Fertil Steril<\/i> 1996; 66: 327\u2013330.","DOI":"10.1016\/S0015-0282(16)58461-1"},{"key":"79","doi-asserted-by":"crossref","unstructured":"79. Tamessar CT, Anderson AL, Bromfield EG, Trigg NA, Parameswaran S, Stanger SJ, Weidenhofer J, Zhang HM, Robertson SA, Sharkey DJ, Nixon B, Schjenken JE. The efficacy and functional consequences of interactions between human spermatozoa and seminal fluid extracellular vesicles. Reprod Fertil<\/i> 2024; 5: 5.","DOI":"10.1530\/RAF-23-0088"},{"key":"80","doi-asserted-by":"crossref","unstructured":"80. Aum\u00fcller G, Riva A. Morphology and functions of the human seminal vesicle. Andrologia<\/i> 1992; 24: 183\u2013196.","DOI":"10.1111\/j.1439-0272.1992.tb02636.x"},{"key":"81","doi-asserted-by":"crossref","unstructured":"81. Maegawa M, Kamada M, Irahara M, Yamamoto S, Yoshikawa S, Kasai Y, Ohmoto Y, Gima H, Thaler CJ, Aono T. A repertoire of cytokines in human seminal plasma. J Reprod Immunol<\/i> 2002; 54: 33\u201342.","DOI":"10.1016\/S0165-0378(01)00063-8"},{"key":"82","doi-asserted-by":"crossref","unstructured":"82. Tremellen KP, Seamark RF, Robertson SA. Seminal transforming growth factor beta1 stimulates granulocyte-macrophage colony-stimulating factor production and inflammatory cell recruitment in the murine uterus. Biol Reprod<\/i> 1998; 58: 1217\u20131225.","DOI":"10.1095\/biolreprod58.5.1217"},{"key":"83","doi-asserted-by":"crossref","unstructured":"83. Sharkey DJ, Macpherson AM, Tremellen KP, Mottershead DG, Gilchrist RB, Robertson SA. TGF-\u03b2 mediates proinflammatory seminal fluid signaling in human cervical epithelial cells. J Immunol<\/i> 2012; 189: 1024\u20131035.","DOI":"10.4049\/jimmunol.1200005"},{"key":"84","doi-asserted-by":"crossref","unstructured":"84. O\u2019Leary S, Armstrong DT, Robertson SA. Transforming growth factor-\u03b2 (TGF\u03b2) in porcine seminal plasma. Reprod Fertil Dev<\/i> 2011; 23: 748\u2013758.","DOI":"10.1071\/RD11001"},{"key":"85","unstructured":"85. Scott JL, Ketheesan N, Summers PM. Presence of TGFbeta but not IL-8 or GM-CSF in ram seminal plasma. Society of Reproductive Biology. Gold Coast, Queensland; 2006: 49."},{"key":"86","doi-asserted-by":"crossref","unstructured":"86. Templeton AA, Cooper I, Kelly RW. Prostaglandin concentrations in the semen of fertile men. J Reprod Fertil<\/i> 1978; 52: 147\u2013150.","DOI":"10.1530\/jrf.0.0520147"},{"key":"87","doi-asserted-by":"crossref","unstructured":"87. Denison FC, Calder AA, Kelly RW. The action of prostaglandin E2 on the human cervix: stimulation of interleukin 8 and inhibition of secretory leukocyte protease inhibitor. Am J Obstet Gynecol<\/i> 1999; 180: 614\u2013620.","DOI":"10.1016\/S0002-9378(99)70263-2"},{"key":"88","doi-asserted-by":"crossref","unstructured":"88. Claus R, Dimmick MA, Gimenez T, Hudson LW. Estrogens and prostaglandin F2alpha in the semen and blood plasma of stallions. Theriogenology<\/i> 1992; 38: 687\u2013693.","DOI":"10.1016\/0093-691X(92)90031-L"},{"key":"89","doi-asserted-by":"crossref","unstructured":"89. Gutsche S, von Wolff M, Strowitzki T, Thaler CJ. Seminal plasma induces mRNA expression of IL-1beta, IL-6 and LIF in endometrial epithelial cells in vitro. Mol Hum Reprod<\/i> 2003; 9: 785\u2013791.","DOI":"10.1093\/molehr\/gag095"},{"key":"90","doi-asserted-by":"crossref","unstructured":"90. Larsen MH, Bzorek M, Pass MB, Larsen LG, Nielsen MW, Svendsen SG, Lindhard A, Hviid TV. Human leukocyte antigen-G in the male reproductive system and in seminal plasma. Mol Hum Reprod<\/i> 2011; 17: 727\u2013738.","DOI":"10.1093\/molehr\/gar052"},{"key":"91","doi-asserted-by":"crossref","unstructured":"91. Schaefer TM, Desouza K, Fahey JV, Beagley KW, Wira CR. Toll-like receptor (TLR) expression and TLR-mediated cytokine\/chemokine production by human uterine epithelial cells. Immunology<\/i> 2004; 112: 428\u2013436.","DOI":"10.1111\/j.1365-2567.2004.01898.x"},{"key":"92","doi-asserted-by":"crossref","unstructured":"92. Chan HY, Moldenhauer LM, Groome HM, Schjenken JE, Robertson SA. Toll-like receptor-4 null mutation causes fetal loss and fetal growth restriction associated with impaired maternal immune tolerance in mice. Sci Rep<\/i> 2021; 11: 16569.","DOI":"10.1038\/s41598-021-95213-1"},{"key":"93","doi-asserted-by":"crossref","unstructured":"93. Schjenken JE, Glynn DJ, Sharkey DJ, Robertson SA. TLR4 signaling is a major mediator of the female tract response to seminal fluid in mice. Biol Reprod<\/i> 2015; 93: 68.","DOI":"10.1095\/biolreprod.114.125740"},{"key":"94","doi-asserted-by":"crossref","unstructured":"94. Ezz MA, Marey MA, Elweza AE, Kawai T, Heppelmann M, Pfarrer C, Balboula AZ, Montaser A, Imakawa K, Zaabel SM, Shimada M, Miyamoto A. TLR2\/4 signaling pathway mediates sperm-induced inflammation in bovine endometrial epithelial cells in vitro. PLoS One<\/i> 2019; 14: e0214516.","DOI":"10.1371\/journal.pone.0214516"},{"key":"95","doi-asserted-by":"crossref","unstructured":"95. Zandieh Z, Govahi A, Aghamajidi A, Raoufi E, Amjadi F, Aghajanpour S, Golestan M, Aflatoonian R. TLR-1, TLR-2, and TLR-6 MYD88-dependent signaling pathway: A potential factor in the interaction of high-DNA fragmentation human sperm with fallopian tube epithelial cells. Clin Exp Reprod Med<\/i> 2023; 50: 44\u201352.","DOI":"10.5653\/cerm.2022.05610"},{"key":"96","doi-asserted-by":"crossref","unstructured":"96. Sharkey DJ, Glynn DJ, Schjenken JE, Tremellen KP, Robertson SA. Interferon-gamma inhibits seminal plasma induction of colony-stimulating factor 2 in mouse and human reproductive tract epithelial cells. Biol Reprod<\/i> 2018; 99: 514\u2013526.","DOI":"10.1093\/biolre\/ioy071"},{"key":"97","doi-asserted-by":"crossref","unstructured":"97. Schjenken JE, Moldenhauer LM, Sharkey DJ, Chan HY, Chin PY, Fullston T, McPherson NO, Robertson SA. High-fat Diet Alters Male Seminal Plasma Composition to Impair Female Immune Adaptation for Pregnancy in Mice. Endocrinology<\/i> 2021; 162: bqab123.","DOI":"10.1210\/endocr\/bqab123"},{"key":"98","doi-asserted-by":"crossref","unstructured":"98. Skerrett-Byrne DA, Nixon B, Bromfield EG, Breen J, Trigg NA, Stanger SJ, Bernstein IR, Anderson AL, Lord T, Aitken RJ, Roman SD, Robertson SA, Schjenken JE. Transcriptomic analysis of the seminal vesicle response to the reproductive toxicant acrylamide. BMC Genomics<\/i> 2021; 22: 728.","DOI":"10.1186\/s12864-021-07951-1"},{"key":"99","doi-asserted-by":"crossref","unstructured":"99. Skerrett-Byrne DA, Trigg NA, Bromfield EG, Dun MD, Bernstein IR, Anderson AL, Stanger SJ, MacDougall LA, Lord T, Aitken RJ, Roman SD, Robertson SA, Nixon B, Schjenken JE. Proteomic dissection of the impact of environmental exposures on mouse seminal vesicle function. Mol Cell Proteomics<\/i> 2021; 20: 100107.","DOI":"10.1016\/j.mcpro.2021.100107"},{"key":"100","doi-asserted-by":"crossref","unstructured":"100. Lyons HE, Arman BM, Robertson SA, Sharkey DJ. Immune regulatory cytokines in seminal plasma of healthy men: A scoping review and analysis of variance. Andrology<\/i> 2023; 11: 1245\u20131266.","DOI":"10.1111\/andr.13424"},{"key":"101","doi-asserted-by":"crossref","unstructured":"101. Kershaw-Young CM, Druart X, Vaughan J, Maxwell WM. \u03b2-Nerve growth factor is a major component of alpaca seminal plasma and induces ovulation in female alpacas. Reprod Fertil Dev<\/i> 2012; 24: 1093\u20131097.","DOI":"10.1071\/RD12039"},{"key":"102","doi-asserted-by":"crossref","unstructured":"102. Ulloa-Leal C, Bogle OA, Adams GP, Ratto MH. Luteotrophic effect of ovulation-inducing factor\/nerve growth factor present in the seminal plasma of llamas. Theriogenology<\/i> 2014; 81: 1101\u20131107.e1.","DOI":"10.1016\/j.theriogenology.2014.01.038"},{"key":"103","doi-asserted-by":"crossref","unstructured":"103. Silva M, Ulloa-Leal C, Norambuena C, Fern\u00e1ndez A, Adams GP, Ratto MH. Ovulation-inducing factor (OIF\/NGF) from seminal plasma origin enhances Corpus Luteum function in llamas regardless the preovulatory follicle diameter. Anim Reprod Sci<\/i> 2014; 148: 221\u2013227.","DOI":"10.1016\/j.anireprosci.2014.05.012"},{"key":"104","doi-asserted-by":"crossref","unstructured":"104. Maranesi M, Boiti C, Zerani M. Nerve Growth Factor (NGF) and Animal Reproduction. Adv Exp Med Biol<\/i> 2021; 1331: 277\u2013287.","DOI":"10.1007\/978-3-030-74046-7_19"},{"key":"105","doi-asserted-by":"crossref","unstructured":"105. Ma Y, Yu X, Liu YF, Song B, Sun Z, Zhao S. Immunoregulation and male reproductive function: Impacts and mechanistic insights into inflammation. Andrology<\/i> 2025; 13: 1302\u20131321.","DOI":"10.1111\/andr.13772"},{"key":"106","doi-asserted-by":"crossref","unstructured":"106. Moldenhauer LM, Keenihan SN, Hayball JD, Robertson SA. GM-CSF is an essential regulator of T cell activation competence in uterine dendritic cells during early pregnancy in mice. J Immunol<\/i> 2010; 185: 7085\u20137096.","DOI":"10.4049\/jimmunol.1001374"},{"key":"107","doi-asserted-by":"crossref","unstructured":"107. McMaster MT, Newton RC, Dey SK, Andrews GK. Activation and distribution of inflammatory cells in the mouse uterus during the preimplantation period. J Immunol<\/i> 1992; 148: 1699\u20131705.","DOI":"10.4049\/jimmunol.148.6.1699"},{"key":"108","doi-asserted-by":"crossref","unstructured":"108. Chan HY, Tran HM, Breen J, Schjenken JE, Robertson SA. The endometrial transcriptome transition preceding receptivity to embryo implantation in mice. BMC Genomics<\/i> 2023; 24: 590.","DOI":"10.1186\/s12864-023-09698-3"},{"key":"109","doi-asserted-by":"crossref","unstructured":"109. Robertson SA, Chin PY, Glynn DJ, Thompson JG. Peri-conceptual cytokines--setting the trajectory for embryo implantation, pregnancy and beyond. Am J Reprod Immunol<\/i> 2011; 66(Suppl 1): 2\u201310.","DOI":"10.1111\/j.1600-0897.2011.01039.x"},{"key":"110","doi-asserted-by":"crossref","unstructured":"110. Jasper MJ, Care AS, Sullivan B, Ingman WV, Aplin JD, Robertson SA. Macrophage-derived LIF and IL1B regulate alpha(1,2)fucosyltransferase 2 (Fut2) expression in mouse uterine epithelial cells during early pregnancy. Biol Reprod<\/i> 2011; 84: 179\u2013188.","DOI":"10.1095\/biolreprod.110.085399"},{"key":"111","doi-asserted-by":"crossref","unstructured":"111. Gangnuss S, Sutton-McDowall ML, Robertson SA, Armstrong DT. Seminal plasma regulates corpora lutea macrophage populations during early pregnancy in mice. Biol Reprod<\/i> 2004; 71: 1135\u20131141.","DOI":"10.1095\/biolreprod.104.027425"},{"key":"112","doi-asserted-by":"crossref","unstructured":"112. Care AS, Diener KR, Jasper MJ, Brown HM, Ingman WV, Robertson SA. Macrophages regulate corpus luteum development during embryo implantation in mice. J Clin Invest<\/i> 2013; 123: 3472\u20133487.","DOI":"10.1172\/JCI60561"},{"key":"113","doi-asserted-by":"crossref","unstructured":"113. Aluvihare VR, Kallikourdis M, Betz AG. Regulatory T cells mediate maternal tolerance to the fetus. Nat Immunol<\/i> 2004; 5: 266\u2013271.","DOI":"10.1038\/ni1037"},{"key":"114","doi-asserted-by":"crossref","unstructured":"114. Zhao JX, Zeng YY, Liu Y. Fetal alloantigen is responsible for the expansion of the CD4(+)CD25(+) regulatory T cell pool during pregnancy. J Reprod Immunol<\/i> 2007; 75: 71\u201381.","DOI":"10.1016\/j.jri.2007.06.052"},{"key":"115","doi-asserted-by":"crossref","unstructured":"115. Chen W, Jin W, Hardegen N, Lei KJ, Li L, Marinos N, McGrady G, Wahl SM. Conversion of peripheral CD4+CD25- naive T cells to CD4+CD25+ regulatory T cells by TGF-beta induction of transcription factor Foxp3. J Exp Med<\/i> 2003; 198: 1875\u20131886.","DOI":"10.1084\/jem.20030152"},{"key":"116","doi-asserted-by":"crossref","unstructured":"116. Clark DA, Fernandes J, Banwatt D. Prevention of spontaneous abortion in the CBA x DBA\/2 mouse model by intravaginal TGF-beta and local recruitment of CD4+8+ FOXP3+ cells. Am J Reprod Immunol<\/i> 2008; 59: 525\u2013534.","DOI":"10.1111\/j.1600-0897.2008.00582.x"},{"key":"117","doi-asserted-by":"crossref","unstructured":"117. Foyle KL, Chan HY, Tran HM, Breen J, Schjenken JE, Robertson SA. Seminal fluid expands the uterine gamma\/delta T cell pool during early pregnancy in mice. Mucosal Immunol<\/i> 2025.","DOI":"10.1016\/j.mucimm.2025.11.009"},{"key":"118","doi-asserted-by":"crossref","unstructured":"118. Foyle KL, Robertson SA. Gamma delta (\u03b3\u03b4) T cells in the female reproductive tract: active participants or indifferent bystanders in reproductive success? Discov Immunol<\/i> 2024; 3: kyae004.","DOI":"10.1093\/discim\/kyae004"},{"key":"119","doi-asserted-by":"crossref","unstructured":"119. Pang SF, Chow PH, Wong TM. The role of the seminal vesicles, coagulating glands and prostate glands on the fertility and fecundity of mice. J Reprod Fertil<\/i> 1979; 56: 129\u2013132.","DOI":"10.1530\/jrf.0.0560129"},{"key":"120","doi-asserted-by":"crossref","unstructured":"120. Queen K, Dhabuwala CB, Pierrepoint CG. The effect of the removal of the various accessory sex glands on the fertility of male rats. J Reprod Fertil<\/i> 1981; 62: 423\u2013426.","DOI":"10.1530\/jrf.0.0620423"},{"key":"121","doi-asserted-by":"crossref","unstructured":"121. Peitz B, Olds-Clarke P. Effects of seminal vesicle removal on fertility and uterine sperm motility in the house mouse. Biol Reprod<\/i> 1986; 35: 608\u2013617.","DOI":"10.1095\/biolreprod35.3.608"},{"key":"122","doi-asserted-by":"crossref","unstructured":"122. O WS, Chen HQ, Chow PH. Effects of male accessory sex gland secretions on early embryonic development in the golden hamster. J Reprod Fertil<\/i> 1988; 84: 341\u2013344.","DOI":"10.1530\/jrf.0.0840341"},{"key":"123","doi-asserted-by":"crossref","unstructured":"123. Watson JG, Carroll J, Chaykin S. Reproduction in mice: The fate of spermatozoa not involved in fertilization. Gamete Res<\/i> 1983; 7: 75\u201384.","DOI":"10.1002\/mrd.1120070107"},{"key":"124","doi-asserted-by":"crossref","unstructured":"124. Carp HJ, Serr DM, Mashiach S, Nebel L. Influence of insemination on the implantation of transferred rat blastocysts. Gynecol Obstet Invest<\/i> 1984; 18: 194\u2013198.","DOI":"10.1159\/000299080"},{"key":"125","doi-asserted-by":"crossref","unstructured":"125. Chan HY, Robertson SA. Seminal fluid effects on uterine receptivity to embryo implantation: transcriptomic strategies to define molecular mechanisms. Reprod Fertil Dev<\/i> 2025; 37: RD24162.","DOI":"10.1071\/RD24162"},{"key":"126","doi-asserted-by":"crossref","unstructured":"126. Br\u00e4nnstr\u00f6m M, MacLennan AH. Relaxin induces ovulations in the in-vitro perfused rat ovary. Hum Reprod<\/i> 1993; 8: 1011\u20131014.","DOI":"10.1093\/oxfordjournals.humrep.a138184"},{"key":"127","doi-asserted-by":"crossref","unstructured":"127. Glynn DJ, Heng K, Russell DL, Sharkey DJ, Robertson SA, Anand-Ivell R, Ivell R. Male seminal relaxin contributes to induction of the post-mating cytokine response in the female mouse uterus. Front Physiol<\/i> 2017; 8: 422.","DOI":"10.3389\/fphys.2017.00422"},{"key":"128","doi-asserted-by":"crossref","unstructured":"128. Pudney J, Quayle AJ, Anderson DJ. Immunological microenvironments in the human vagina and cervix: mediators of cellular immunity are concentrated in the cervical transformation zone. Biol Reprod<\/i> 2005; 73: 1253\u20131263.","DOI":"10.1095\/biolreprod.105.043133"},{"key":"129","doi-asserted-by":"crossref","unstructured":"129. Sharkey DJ, Macpherson AM, Tremellen KP, Robertson SA. Seminal plasma differentially regulates inflammatory cytokine gene expression in human cervical and vaginal epithelial cells. Mol Hum Reprod<\/i> 2007; 13: 491\u2013501.","DOI":"10.1093\/molehr\/gam028"},{"key":"130","doi-asserted-by":"crossref","unstructured":"130. Ochsenk\u00fchn R, Toth B, Nieschlag E, Artman E, Friese K, Thaler CJ. Seminal plasma stimulates cytokine production in endometrial epithelial cell cultures independently of the presence of leucocytes. Andrologia<\/i> 2008; 40: 364\u2013369.","DOI":"10.1111\/j.1439-0272.2008.00870.x"},{"key":"131","doi-asserted-by":"crossref","unstructured":"131. McGuane JT, Watson KM, Zhang J, Johan MZ, Wang Z, Kuo G, Sharkey DJ, Robertson SA, Hull ML. Seminal plasma promotes lesion development in a xenograft model of endometriosis. Am J Pathol<\/i> 2015; 185: 1409\u20131422.","DOI":"10.1016\/j.ajpath.2015.01.010"},{"key":"132","doi-asserted-by":"crossref","unstructured":"132. van den Berg JS, Toros M, Abendroth MS, Zhang Y, Arends B, Verpoest WMJA, Broekmans FJM, Steba GS. Seminal plasma induces receptivity-associated genes and pathways in endometrial epithelial organoids. Reprod Biomed Online<\/i> 2025; 51: 104982.","DOI":"10.1016\/j.rbmo.2025.104982"},{"key":"133","doi-asserted-by":"crossref","unstructured":"133. Doyle U, Sampson N, Zenzmaier C, Schw\u00e4rzler P, Berger P. Seminal plasma enhances and accelerates progesterone-induced decidualisation of human endometrial stromal cells. Reprod Fertil Dev<\/i> 2012; 24: 517\u2013522.","DOI":"10.1071\/RD10296"},{"key":"134","doi-asserted-by":"crossref","unstructured":"134. Chen JC, Johnson BA, Erikson DW, Piltonen TT, Barragan F, Chu S, Kohgadai N, Irwin JC, Greene WC, Giudice LC, Roan NR. Seminal plasma induces global transcriptomic changes associated with cell migration, proliferation and viability in endometrial epithelial cells and stromal fibroblasts. Hum Reprod<\/i> 2014; 29: 1255\u20131270.","DOI":"10.1093\/humrep\/deu047"},{"key":"135","doi-asserted-by":"crossref","unstructured":"135. Kunz G, Beil D, Deininger H, Wildt L, Leyendecker G. The dynamics of rapid sperm transport through the female genital tract: evidence from vaginal sonography of uterine peristalsis and hysterosalpingoscintigraphy. Hum Reprod<\/i> 1996; 11: 627\u2013632.","DOI":"10.1093\/HUMREP\/11.3.627"},{"key":"136","doi-asserted-by":"crossref","unstructured":"136. Kimura H, Fukui A, Fujii S, Yamaguchi E, Kasai G, Mizunuma H. Timed sexual intercourse facilitates the recruitment of uterine CD56(bright) natural killer cells in women with infertility. Am J Reprod Immunol<\/i> 2009; 62: 118\u2013124.","DOI":"10.1111\/j.1600-0897.2009.00720.x"},{"key":"137","doi-asserted-by":"crossref","unstructured":"137. Catalini L, Burton M, Egeberg DL, Eskildsen TV, Thomassen M, Fedder J. In vivo effect of vaginal seminal plasma application on the human endometrial transcriptome: a randomized controlled trial. Mol Hum Reprod<\/i> 2024; 30: 30.","DOI":"10.1093\/molehr\/gaae017"},{"key":"138","doi-asserted-by":"crossref","unstructured":"138. Remes Lenicov F, Rodriguez Rodrigues C, Sabatt\u00e9 J, Cabrini M, Jancic C, Ostrowski M, Merlotti A, Gonzalez H, Alonso A, Pasqualini RA, Davio C, Geffner J, Ceballos A. Semen promotes the differentiation of tolerogenic dendritic cells. J Immunol<\/i> 2012; 189: 4777\u20134786.","DOI":"10.4049\/jimmunol.1202089"},{"key":"139","doi-asserted-by":"crossref","unstructured":"139. Dekker G, Robillard PY, Roberts C. The etiology of preeclampsia: the role of the father. J Reprod Immunol<\/i> 2011; 89: 126\u2013132.","DOI":"10.1016\/j.jri.2010.12.010"},{"key":"140","doi-asserted-by":"crossref","unstructured":"140. Di Mascio D, Saccone G, Bellussi F, Vitagliano A, Berghella V. Type of paternal sperm exposure before pregnancy and the risk of preeclampsia: A systematic review. Eur J Obstet Gynecol Reprod Biol<\/i> 2020; 251: 246\u2013253.","DOI":"10.1016\/j.ejogrb.2020.05.065"},{"key":"141","doi-asserted-by":"crossref","unstructured":"141. Saccone G, Di Spiezio Sardo A, Ciardulli A, Caissutti C, Spinelli M, Surbek D, von Wolff M. Effectiveness of seminal plasma in in vitro fertilisation treatment: a systematic review and meta-analysis. BJOG<\/i> 2019; 126: 220\u2013225.","DOI":"10.1111\/1471-0528.15004"},{"key":"142","unstructured":"142. Lovell JW, Getty R. Fate of semen in the uterus of the sow: histologic study of endometrium during the 27 hours after natural service. Am J Vet Res<\/i> 1968; 29: 609\u2013625."},{"key":"143","unstructured":"143. Claus R. Physiological role of seminal components in the reproductive tract of the female pig. J Reprod Fertil Suppl<\/i> 1990; 40: 117\u2013131."},{"key":"144","doi-asserted-by":"crossref","unstructured":"144. Jiwakanon J, Persson E, Berg M, Dalin AM. Influence of seminal plasma, spermatozoa and semen extender on cytokine expression in the porcine endometrium after insemination. Anim Reprod Sci<\/i> 2011; 123: 210\u2013220.","DOI":"10.1016\/j.anireprosci.2010.11.016"},{"key":"145","doi-asserted-by":"crossref","unstructured":"145. Taylor U, Rath D, Zerbe H, Schuberth HJ. Interaction of intact porcine spermatozoa with epithelial cells and neutrophilic granulocytes during uterine passage. Reprod Domest Anim<\/i> 2008; 43: 166\u2013175.","DOI":"10.1111\/j.1439-0531.2007.00872.x"},{"key":"146","doi-asserted-by":"crossref","unstructured":"146. Bischof RJ, Lee CS, Brandon MR, Meeusen E. Inflammatory response in the pig uterus induced by seminal plasma. J Reprod Immunol<\/i> 1994; 26: 131\u2013146.","DOI":"10.1016\/0165-0378(94)90036-1"},{"key":"147","doi-asserted-by":"crossref","unstructured":"147. Bischof RJ, Brandon MR, Lee CS. Cellular immune responses in the pig uterus during pregnancy. J Reprod Immunol<\/i> 1995; 29: 161\u2013178.","DOI":"10.1016\/0165-0378(95)00935-E"},{"key":"148","unstructured":"148. Engelhardt H, Croy BA, King GJ. Role of uterine immune cells in early pregnancy in pigs. J Reprod Fertil Suppl<\/i> 1997; 52: 115\u2013131."},{"key":"149","doi-asserted-by":"crossref","unstructured":"149. Madej M, Norrby M, Madsen M, Johannisson A, Hansen C, Madej A. The effect of boar seminal plasma on the release of prostaglandins and interleukin-6 by porcine endometrial and cervical cells and bovine endometrial cells. Reprod Domest Anim<\/i> 2012; 47: 113\u2013124.","DOI":"10.1111\/j.1439-0531.2011.01809.x"},{"key":"150","doi-asserted-by":"crossref","unstructured":"150. Martinez CA, Cambra JM, Parrilla I, Roca J, Ferreira-Dias G, Pallares FJ, Lucas X, Vazquez JM, Martinez EA, Gil MA, Rodriguez-Martinez H, Cuello C, \u00c1lvarez-Rodriguez M. Seminal plasma modifies the transcriptional pattern of the endometrium and advances embryo development in pigs. Front Vet Sci<\/i> 2019; 6: 465.","DOI":"10.3389\/fvets.2019.00465"},{"key":"151","doi-asserted-by":"crossref","unstructured":"151. Gardela J, Ruiz-Conca M, Martinez CA, Wright D, L\u00f3pez-B\u00e9jar M, Rodriguez-Martinez H, Alvarez-Rodriguez M. The expression of cold-inducible RNA-binding protein mRNA in sow genital tract is modulated by natural mating, but not by seminal plasma. Int J Mol Sci<\/i> 2020; 21: 5333.","DOI":"10.3390\/ijms21155333"},{"key":"152","doi-asserted-by":"crossref","unstructured":"152. Gardela J, Ruiz-Conca M, Wright D, L\u00f3pez-B\u00e9jar M, Mart\u00ednez CA, Rodr\u00edguez-Mart\u00ednez H, \u00c1lvarez-Rodr\u00edguez M. Semen modulates cell proliferation and differentiation-related transcripts in the pig peri-ovulatory endometrium. Biology (Basel)<\/i> 2022; 11: 11.","DOI":"10.3390\/biology11040616"},{"key":"153","doi-asserted-by":"crossref","unstructured":"153. \u00c1lvarez-Rodr\u00edguez M, Roca J, Mart\u00ednez EA, Rodr\u00edguez-Mart\u00ednez H. Mating modifies the expression of crucial oxidative-reductive transcripts in the pig oviductal sperm reservoir: is the female ensuring sperm survival? Front Endocrinol (Lausanne)<\/i> 2023; 14: 1042176.","DOI":"10.3389\/fendo.2023.1042176"},{"key":"154","doi-asserted-by":"crossref","unstructured":"154. O\u2019Leary S, Jasper MJ, Warnes GM, Armstrong DT, Robertson SA. Seminal plasma regulates endometrial cytokine expression, leukocyte recruitment and embryo development in the pig. Reproduction<\/i> 2004; 128: 237\u2013247.","DOI":"10.1530\/rep.1.00160"},{"key":"155","doi-asserted-by":"crossref","unstructured":"155. Parrilla I, Martinez CA, Cambra JM, Lucas X, Ferreira-Dias G, Rodriguez-Martinez H, Cuello C, Gil MA, Martinez EA. Blastocyst-bearing sows display a dominant anti-inflammatory cytokine profile compared to cyclic sows at day 6 of the cycle. Animals (Basel)<\/i> 2020; 10: 10.","DOI":"10.3390\/ani10112028"},{"key":"156","doi-asserted-by":"crossref","unstructured":"156. Barranco I, Padilla L, Martinez CA, Alvarez-Rodriguez M, Parrilla I, Lucas X, Ferreira-Dias G, Yeste M, Rodriguez-Martinez H, Roca J. Seminal plasma modulates miRNA expression by sow genital tract lining explants. Biomolecules<\/i> 2020; 10: 933.","DOI":"10.3390\/biom10060933"},{"key":"157","doi-asserted-by":"crossref","unstructured":"157. Taylor U, Zerbe H, Seyfert HM, Rath D, Baulain U, Langner KF, Schuberth HJ. Porcine spermatozoa inhibit post-breeding cytokine induction in uterine epithelial cells in vivo. Anim Reprod Sci<\/i> 2009; 115: 279\u2013289.","DOI":"10.1016\/j.anireprosci.2008.11.019"},{"key":"158","doi-asserted-by":"crossref","unstructured":"158. Rodriguez-Martinez H, Saravia F, Wallgren M, Martinez EA, Sanz L, Roca J, Vazquez JM, Calvete JJ. Spermadhesin PSP-I\/PSP-II heterodimer induces migration of polymorphonuclear neutrophils into the uterine cavity of the sow. J Reprod Immunol<\/i> 2010; 84: 57\u201365.","DOI":"10.1016\/j.jri.2009.10.007"},{"key":"159","doi-asserted-by":"crossref","unstructured":"159. Kaczmarek MM, Krawczynski K, Filant J. Seminal plasma affects prostaglandin synthesis and angiogenesis in the porcine uterus. Biol Reprod<\/i> 2013; 88: 72.","DOI":"10.1095\/biolreprod.112.103564"},{"key":"160","doi-asserted-by":"crossref","unstructured":"160. Toledo-Guardiola SM, P\u00e1rraga-Ros E, Seva J, Luongo C, Garc\u00eda-V\u00e1zquez FA, Soriano-\u00dabeda C, Mat\u00e1s C. Artificial insemination of all ejaculated sperm fractions accelerates embryo development and increases the uterine vascularity in the pig. Theriogenology<\/i> 2024; 219: 32\u201338.","DOI":"10.1016\/j.theriogenology.2024.02.017"},{"key":"161","doi-asserted-by":"crossref","unstructured":"161. Signoret JP, Du Mesnil du Buisson F, Maul\u00e9on P. Effect of mating on the onset and duration of ovulation in the sow. J Reprod Fertil<\/i> 1972; 31: 327\u2013330.","DOI":"10.1530\/jrf.0.0310327"},{"key":"162","doi-asserted-by":"crossref","unstructured":"162. Waberski D, Kremer H, Borchardt Neto G, Jungblut PW, Kallweit E, Weitze KF. Studies on a local effect of boar seminal plasma on ovulation time in gilts. Zentralbl Veterin\u00e4rmed A<\/i> 1999; 46: 431\u2013438.","DOI":"10.1046\/j.1439-0442.1999.00230.x"},{"key":"163","doi-asserted-by":"crossref","unstructured":"163. Barranco I, Rub\u00e9r M, Perez-Pati\u00f1o C, Atikuzzaman M, Martinez EA, Roca J, Rodriguez-Martinez H. The seminal plasma of the boar is rich in cytokines, with significant individual and intra-ejaculate variation. Am J Reprod Immunol<\/i> 2015; 74: 523\u2013532.","DOI":"10.1111\/aji.12432"},{"key":"164","doi-asserted-by":"crossref","unstructured":"164. Bai R, Latifi Z, Kusama K, Nakamura K, Shimada M, Imakawa K. Induction of immune-related gene expression by seminal exosomes in the porcine endometrium. Biochem Biophys Res Commun<\/i> 2018; 495: 1094\u20131101.","DOI":"10.1016\/j.bbrc.2017.11.100"},{"key":"165","doi-asserted-by":"crossref","unstructured":"165. Parra A, Mart\u00ednez-D\u00edaz P, Bot\u00eda M, L\u00f3pez-Arjona M, Lucas X, Barranco I, Roca J. The extracellular vesicles of boar seminal plasma contain oxytocin at levels associated with fertility. Extracell Vesicles Circ Nucl Acids<\/i> 2025; 6: 1000\u20131014.","DOI":"10.20517\/evcna.2025.94"},{"key":"166","doi-asserted-by":"crossref","unstructured":"166. Stan\u010di\u0107 I, Radovi\u0107 I, Dragin S, Mirkov M, Pihler I, Horvatovi\u0107 MP, Api\u0107 J, Zdraveski I. Influence of transcervical infusion of seminal plasma on the farrowing rate and litter size in artificially inseminated sows. Arq Bras Med Vet Zootec<\/i> 2020; 72: 1691\u20131697.","DOI":"10.1590\/1678-4162-11227"},{"key":"167","unstructured":"167. Flowers WL, Esbenshade KL. Optimizing management of natural and artificial matings in swine. J Reprod Fertil Suppl<\/i> 1993; 48: 217\u2013228."},{"key":"168","doi-asserted-by":"crossref","unstructured":"168. Murray FA, Grifo AP Jr, Parker CF. Increased litter size in gilts by intrauterine infusion of seminal and sperm antigens before breeding. J Anim Sci<\/i> 1983; 56: 895\u2013900.","DOI":"10.2527\/jas1983.564895x"},{"key":"169","doi-asserted-by":"crossref","unstructured":"169. Phillips DM, Mahler S. Phagocytosis of spermatozoa by the rabbit vagina. Anat Rec<\/i> 1977; 189: 61\u201371.","DOI":"10.1002\/ar.1091890105"},{"key":"170","doi-asserted-by":"crossref","unstructured":"170. Castellini C, Lattaioli P, Moroni M, Minelli A. Effect of seminal plasma on the characteristics and fertility of rabbit spermatozoa. Anim Reprod Sci<\/i> 2000; 63: 275\u2013282.","DOI":"10.1016\/S0378-4320(00)00181-0"},{"key":"171","doi-asserted-by":"crossref","unstructured":"171. Gardela J, Jauregi-Miguel A, Martinez CA, Rodr\u00edguez-Martinez H, L\u00f3pez-B\u00e9jar M, \u00c1lvarez-Rodr\u00edguez M. Semen modulates inflammation and angiogenesis in the reproductive tract of female rabbits. Animals (Basel)<\/i> 2020; 10: 10.","DOI":"10.3390\/ani10122207"},{"key":"172","doi-asserted-by":"crossref","unstructured":"172. Gardela J, Jauregi-Miguel A, Martinez CA, Rodriguez-Martinez H, Lopez-Bejar M, Alvarez-Rodriguez M. Semen Modulates the Expression of NGF, ABHD2, VCAN, and CTEN in the Reproductive Tract of Female Rabbits. Genes (Basel)<\/i> 2020; 11: 758.","DOI":"10.3390\/genes11070758"},{"key":"173","doi-asserted-by":"crossref","unstructured":"173. Ruiz-Conca M, Gardela J, Jauregi-Miguel A, Martinez CA, Rodr\u00edguez-Martinez H, L\u00f3pez-B\u00e9jar M, Alvarez-Rodriguez M. Seminal plasma triggers the differential expression of the glucocorticoid receptor (NR3C1\/GR<\/i>) in the rabbit reproductive tract. Animals (Basel)<\/i> 2020; 10: 10.","DOI":"10.3390\/ani10112158"},{"key":"174","doi-asserted-by":"crossref","unstructured":"174. Jappel D. Rapid transport of seminal immunoglobulin to distal parts of the female reproductive tract in rabbits. J Reprod Fertil<\/i> 1992; 96: 135\u2013139.","DOI":"10.1530\/jrf.0.0960135"},{"key":"175","doi-asserted-by":"crossref","unstructured":"175. Guelfi G, Dall\u2019Aglio C, Bufalari A, Mercati F, Anipchenko P, Capaccia C, Cocci P, Palermo FA, Acuti G, Troisi A, Tomassoni D, Boiti C, Zerani M, Maranesi M. Interleukin-1 beta (IL1B) and nerve growth factor (NGF): key players in rabbit reproductive regulation. Int J Mol Sci<\/i> 2024; 25: 10986.","DOI":"10.3390\/ijms252010986"},{"key":"176","doi-asserted-by":"crossref","unstructured":"176. Abney TO, Williams WL. Inhibition of sperm capacitation by intrauterine deposition of seminal plasma decapacitation factor. Biol Reprod<\/i> 1970; 2: 14\u201317.","DOI":"10.1095\/biolreprod2.1.14"},{"key":"177","doi-asserted-by":"crossref","unstructured":"177. Katila T. Onset and duration of uterine inflammatory response of mares after insemination with fresh semen. Biol Reprod<\/i> 1995; 52: 515\u2013517.","DOI":"10.1093\/biolreprod\/52.monograph_series1.515"},{"key":"178","doi-asserted-by":"crossref","unstructured":"178. Portus BJ, Reilas T, Katila T. Effect of seminal plasma on uterine inflammation, contractility and pregnancy rates in mares. Equine Vet J<\/i> 2005; 37: 515\u2013519.","DOI":"10.2746\/042516405775314844"},{"key":"179","doi-asserted-by":"crossref","unstructured":"179. Troedsson MH, Loset K, Alghamdi AM, Dahms B, Crabo BG. Interaction between equine semen and the endometrium: the inflammatory response to semen. Anim Reprod Sci<\/i> 2001; 68: 273\u2013278.","DOI":"10.1016\/S0378-4320(01)00164-6"},{"key":"180","doi-asserted-by":"crossref","unstructured":"180. Troedsson MH, Desvousges A, Alghamdi AS, Dahms B, Dow CA, Hayna J, Valesco R, Collahan PT, Macpherson ML, Pozor M, Buhi WC. Components in seminal plasma regulating sperm transport and elimination. Anim Reprod Sci<\/i> 2005; 89: 171\u2013186.","DOI":"10.1016\/j.anireprosci.2005.07.005"},{"key":"181","doi-asserted-by":"crossref","unstructured":"181. Doty AL, Miller LMJ, Fedorka CE, Troedsson MHT. The role of equine seminal plasma derived cysteine rich secretory protein 3 (CRISP3) in the interaction between polymorphonuclear neutrophils (PMNs) and populations of viable or dead spermatozoa, and bacteria. Theriogenology<\/i> 2024; 219: 22\u201331.","DOI":"10.1016\/j.theriogenology.2024.02.014"},{"key":"182","doi-asserted-by":"crossref","unstructured":"182. Fedorka CE, Scoggin KE, Woodward EM, Squires EL, Ball BA, Troedsson M. The effect of select seminal plasma proteins on endometrial mRNA cytokine expression in mares susceptible to persistent mating-induced endometritis. Reprod Domest Anim<\/i> 2017; 52: 89\u201396.","DOI":"10.1111\/rda.12813"},{"key":"183","doi-asserted-by":"crossref","unstructured":"183. Fedorka CE, El-Sheikh-Ali H, Scoggin KE, Coleman S, Humphrey EA, Troutt L, Troedsson MHT. The Effect of Seminal Plasma on the Equine Endometrial Transcriptome. Reprod Domest Anim<\/i> 2024; 59: e14711.","DOI":"10.1111\/rda.14711"},{"key":"184","doi-asserted-by":"crossref","unstructured":"184. Nash DM, Sheldon IM, Herath S, Lane EA. Markers of the uterine innate immune response of the mare. Anim Reprod Sci<\/i> 2010; 119: 31\u201339.","DOI":"10.1016\/j.anireprosci.2009.11.008"},{"key":"185","doi-asserted-by":"crossref","unstructured":"185. L\u00fcttgenau J, Imboden I, Wellnitz O, Romer R, Scaravaggi I, Neves AP, Borel N, Bruckmaier RM, Janett F, Bollwein H. Intrauterine infusion of killed semen adversely affects uterine blood flow and endometrial gene expression of inflammatory cytokines in mares susceptible to persistent breeding-induced endometritis. Theriogenology<\/i> 2021; 163: 18\u201330.","DOI":"10.1016\/j.theriogenology.2020.12.029"},{"key":"186","doi-asserted-by":"crossref","unstructured":"186. Palm F, Walter I, Budik S, Kolodziejek J, Nowotny N, Aurich C. Influence of different semen extenders and seminal plasma on PMN migration and on expression of IL-1beta, IL-6, TNF-alpha and COX-2 mRNA in the equine endometrium. Theriogenology<\/i> 2008; 70: 843\u2013851.","DOI":"10.1016\/j.theriogenology.2008.04.054"},{"key":"187","doi-asserted-by":"crossref","unstructured":"187. Tun\u00f3n A-M , Katila T, Magnusson U, Nummij\u00e4rvi A, Rodriguez-Martinez H. T-cell distribution in two different segments of the equine endometrium 6 and 48 hours after insemination. Theriogenology<\/i> 2000; 54: 835\u2013841.","DOI":"10.1016\/S0093-691X(00)00395-2"},{"key":"188","doi-asserted-by":"crossref","unstructured":"188. Hartmann C, Gerner W, Walter I, Saalm\u00fcller A, Aurich C. Influences of intrauterine semen administration on regulatory T\u00a0lymphocytes in the oestrous mare (Equus caballus). Theriogenology<\/i> 2018; 118: 119\u2013125.","DOI":"10.1016\/j.theriogenology.2018.05.030"},{"key":"189","doi-asserted-by":"crossref","unstructured":"189. Bollwein H, Sowade C, Stolla R. The effect of semen extender, seminal plasma and raw semen on uterine and ovarian blood flow in mares. Theriogenology<\/i> 2003; 60: 607\u2013616.","DOI":"10.1016\/S0093-691X(03)00084-0"},{"key":"190","doi-asserted-by":"crossref","unstructured":"190. Watson ED. Post-breeding endometritis in the mare. Anim Reprod Sci<\/i> 2000; 60-61: 221\u2013232.","DOI":"10.1016\/S0378-4320(00)00110-X"},{"key":"191","doi-asserted-by":"crossref","unstructured":"191. Rota A, Panzani D, Sabatini C, Camillo F. Donkey jack (Equus asinus) semen cryopreservation: studies of seminal parameters, post breeding inflammatory response, and fertility in donkey jennies. Theriogenology<\/i> 2012; 78: 1846\u20131854.","DOI":"10.1016\/j.theriogenology.2012.07.015"},{"key":"192","doi-asserted-by":"crossref","unstructured":"192. Mir\u00f3 J, Vil\u00e9s K, Garc\u00eda W, Jordana J, Yeste M. Effect of donkey seminal plasma on sperm movement and sperm-polymorphonuclear neutrophils attachment in vitro. Anim Reprod Sci<\/i> 2013; 140: 164\u2013172.","DOI":"10.1016\/j.anireprosci.2013.06.007"},{"key":"193","doi-asserted-by":"crossref","unstructured":"193. Vil\u00e9s K, Rabanal R, Rodr\u00edguez-Prado M, Mir\u00f3 J. Influence of seminal plasma on leucocyte migration and amount of COX-2 protein in the jenny endometrium after insemination with frozen-thawed semen. Anim Reprod Sci<\/i> 2013; 143: 57\u201363.","DOI":"10.1016\/j.anireprosci.2013.11.002"},{"key":"194","doi-asserted-by":"crossref","unstructured":"194. Mir\u00f3 J, Mar\u00edn H, Catal\u00e1n J, Papas M, Gacem S, Yeste M. Seminal Plasma, Sperm Concentration, and Sperm-PMN Interaction in the Donkey: An In Vitro Model to Study Endometrial Inflammation at Post-Insemination. Int J Mol Sci<\/i> 2020; 21: 3478.","DOI":"10.3390\/ijms21103478"},{"key":"195","doi-asserted-by":"crossref","unstructured":"195. Vargas JH, Zarco L, Salinas EM, Ur\u00edas-Castro C, Boeta M. Effects of seminal plasma on uterine polymorphonuclear dynamics and fertility of jennies inseminated with glycerol-free, frozen-thawed donkey semen. J Equine Vet Sci<\/i> 2025; 149: 105571.","DOI":"10.1016\/j.jevs.2025.105571"},{"key":"196","doi-asserted-by":"crossref","unstructured":"196. Oliveira PVLF, Segabinazzi LGTM, Crespilho AM, Oliveira JV, Silva AC, Freitas-Dell\u2019Aqua CP, Dell\u2019Aqua JA Jr, Papa FO. Autologous seminal plasma and post-breeding uterine lavage as alternative options to improve fertility rates of jennies inseminated with cryopreserved jack semen. J Equine Vet Sci<\/i> 2025; 150: 105613.","DOI":"10.1016\/j.jevs.2025.105613"},{"key":"197","doi-asserted-by":"crossref","unstructured":"197. Gwathmey TM, Ignotz GG, Mueller JL, Manjunath P, Suarez SS. Bovine seminal plasma proteins PDC-109, BSP-A3, and BSP-30-kDa share functional roles in storing sperm in the oviduct. Biol Reprod<\/i> 2006; 75: 501\u2013507.","DOI":"10.1095\/biolreprod.106.053306"},{"key":"198","doi-asserted-by":"crossref","unstructured":"198. Alghamdi AS, Funnell BJ, Bird SL, Lamb GC, Rendahl AK, Taube PC, Foster DN. Comparative studies on bull and stallion seminal DNase activity and interaction with semen extender and spermatozoa. Anim Reprod Sci<\/i> 2010; 121: 249\u2013258.","DOI":"10.1016\/j.anireprosci.2010.06.003"},{"key":"199","doi-asserted-by":"crossref","unstructured":"199. Donnellan EM, O\u2019Brien MB, Meade KG, Fair S. Comparison of the uterine inflammatory response to frozen-thawed sperm from high and low fertility bulls. Theriogenology<\/i> 2021; 176: 26\u201334.","DOI":"10.1016\/j.theriogenology.2021.09.012"},{"key":"200","doi-asserted-by":"crossref","unstructured":"200. Marey MA, Ma D, Yoshino H, Elesh IF, Zinnah MA, Fiorenza MF, Moriyasu S, Miyamoto A. Sperm induce proinflammatory responses in the uterus and peripheral blood immune cells of artificially inseminated cows. J Reprod Dev<\/i> 2023; 69: 95\u2013102.","DOI":"10.1262\/jrd.2022-124"},{"key":"201","doi-asserted-by":"crossref","unstructured":"201. Garner DL, Thomas CA, Gravance CG, Marshall CE, DeJarnette JM, Allen CH. Seminal plasma addition attenuates the dilution effect in bovine sperm. Theriogenology<\/i> 2001; 56: 31\u201340.","DOI":"10.1016\/S0093-691X(01)00540-4"},{"key":"202","doi-asserted-by":"crossref","unstructured":"202. Baas JW, Molan PC, Shannon P. Factors in seminal plasma of bulls that affect the viability and motility of spermatozoa. J Reprod Fertil<\/i> 1983; 68: 275\u2013280.","DOI":"10.1530\/jrf.0.0680275"},{"key":"203","doi-asserted-by":"crossref","unstructured":"203. Alo\u00e9 S, Weber F, Behr B, Sauter-Louis C, Zerbe H. Modulatory effects of bovine seminal plasma on uterine inflammatory processes. Reprod Domest Anim<\/i> 2012; 47: 12\u201319.","DOI":"10.1111\/j.1439-0531.2011.01792.x"},{"key":"204","doi-asserted-by":"crossref","unstructured":"204. Fichtner T, Kotarski F, Hermosilla C, Taubert A, Wrenzycki C. Semen extender and seminal plasma alter the extent of neutrophil extracellular traps (NET) formation in cattle. Theriogenology<\/i> 2021; 160: 72\u201380.","DOI":"10.1016\/j.theriogenology.2020.10.032"},{"key":"205","doi-asserted-by":"crossref","unstructured":"205. Ibrahim LA, Rizo JA, Fontes PLP, Lamb GC, Bromfield JJ. Seminal plasma modulates expression of endometrial inflammatory meditators in the bovine\u2020. Biol Reprod<\/i> 2019; 100: 660\u2013671.","DOI":"10.1093\/biolre\/ioy226"},{"key":"206","doi-asserted-by":"crossref","unstructured":"206. Ortiz WG, Rizo JA, Carvalheira LR, Ahmed BMS, Estrada-Cortes E, Harstine BR, Bromfield JJ, Hansen PJ. Effects of intrauterine infusion of seminal plasma at artificial insemination on fertility of lactating Holstein cows. J Dairy Sci<\/i> 2019; 102: 6587\u20136594.","DOI":"10.3168\/jds.2019-16251"},{"key":"207","doi-asserted-by":"crossref","unstructured":"207. Elmetwally MA, Meinecke-Tillmann S, Herzog K, Bollwein H. Effects of natural mating, artificial insemination and intravaginal deposition of raw semen or seminal plasma on vaginal and uterine blood flow in German Holstein cows. BMC Vet Res<\/i> 2024; 20: 277.","DOI":"10.1186\/s12917-024-03919-x"},{"key":"208","doi-asserted-by":"crossref","unstructured":"208. Badrakh D, Yanagawa Y, Nagano M, Katagiri S. Effect of seminal plasma infusion into the vagina on the normalization of endometrial epidermal growth factor concentrations and fertility in repeat breeder dairy cows. J Reprod Dev<\/i> 2020; 66: 149\u2013154.","DOI":"10.1262\/jrd.2019-148"},{"key":"209","doi-asserted-by":"crossref","unstructured":"209. Ninpetch N, Badrakh D, Kawano K, Yanagawa Y, Nagano M, Katagiri S, Katagiri S. Leptin receptor expression and its change in association with the normalization of EGF profile after seminal plasma treatment in repeat breeder dairy cows. J Reprod Dev<\/i> 2022; 68: 209\u2013215.","DOI":"10.1262\/jrd.2021-142"},{"key":"210","doi-asserted-by":"crossref","unstructured":"210. Kyaw HM, Sato H, Tagami T, Yanagawa Y, Nagano M, Katagiri S. Effects of milk osteopontin on the endometrial epidermal growth factor profile and restoration of fertility in repeat breeder dairy cows. Theriogenology<\/i> 2022; 184: 26\u201333.","DOI":"10.1016\/j.theriogenology.2022.02.008"},{"key":"211","doi-asserted-by":"crossref","unstructured":"211. Nongbua T, Guo Y, Edman A, Humblot P, Morrell JM. Effect of bovine seminal plasma on bovine endometrial epithelial cells in culture. Reprod Domest Anim<\/i> 2018; 53: 85\u201392.","DOI":"10.1111\/rda.13069"},{"key":"212","doi-asserted-by":"crossref","unstructured":"212. Swanson RM, Arick MA 2nd, Gon\u00e7alves LM, Davis DB, Lawton Stewart R Jr, Fontes PLP, Lemley CO. Seminal plasma from bulls with divergent plane of nutrition minimally alters bovine uterine endometrial epithelial cell gene expression in vitro. J Anim Sci<\/i> 2025; 103: skaf267.","DOI":"10.1093\/jas\/skaf267"},{"key":"213","doi-asserted-by":"crossref","unstructured":"213. Rizo JA, Ibrahim LA, Molinari PCC, Harstine BR, Piersanti RL, Bromfield JJ. Effect of seminal plasma or transforming growth factor on bovine endometrial cells. Reproduction<\/i> 2019; 158: 529\u2013541.","DOI":"10.1530\/REP-19-0421"},{"key":"214","doi-asserted-by":"crossref","unstructured":"214. Fernandez-Fuertes B, S\u00e1nchez JM, Bag\u00e9s-Arnal S, McDonald M, Yeste M, Lonergan P. Species-specific and collection method-dependent differences in endometrial susceptibility to seminal plasma-induced RNA degradation. Sci Rep<\/i> 2019; 9: 15072.","DOI":"10.1038\/s41598-019-51413-4"},{"key":"215","doi-asserted-by":"crossref","unstructured":"215. S\u00e1nchez JM, Rabaglino MB, Bag\u00e9s-Arnal S, McDonald M, Behura SK, Spencer TE, Lonergan P, Fernandez-Fuertes B. Sperm exposure to accessory gland secretions alters the transcriptomic response of the endometrium in cattle. Theriogenology<\/i> 2024; 218: 26\u201334.","DOI":"10.1016\/j.theriogenology.2024.01.037"},{"key":"216","doi-asserted-by":"crossref","unstructured":"216. Odhiambo JF, Poole DH, Hughes L, Dejarnette JM, Inskeep EK, Dailey RA. Pregnancy outcome in dairy and beef cattle after artificial insemination and treatment with seminal plasma or transforming growth factor beta-1. Theriogenology<\/i> 2009; 72: 566\u2013571.","DOI":"10.1016\/j.theriogenology.2009.04.013"},{"key":"217","doi-asserted-by":"crossref","unstructured":"217. Swanson RM, Messman RD, Dobbins TW, Contreras-Correa ZE, Arick MA 2nd, Sidelinger DR, King H, Lemley CO. Seminal plasma uterine priming alters uterine transcriptomics and negatively impacts embryo growth and uterine artery resistance but not offspring liver transcriptomics in beef cattle. J Anim Sci<\/i> 2024; 102: sdae300.","DOI":"10.1093\/jas\/skae300"},{"key":"218","doi-asserted-by":"crossref","unstructured":"218. Fritsche KLM, Ahola JK, Pinedo PJ, Seidel GE, Rhoades RD, Stevenson JS, Olson KC, Jaeger JR, Grieger DM, Bromfield JJ. Pregnancy risk in beef and dairy cows after supplementing semen with transforming growth factor beta-1 at the time of artificial insemination. J Anim Sci<\/i> 2024; 102: skae169.","DOI":"10.1093\/jas\/skae169"},{"key":"219","doi-asserted-by":"crossref","unstructured":"219. Mattner PE. The distribution of spermatozoa and leucocytes in the female genital tract in goats and cattle. J Reprod Fertil<\/i> 1968; 17: 253\u2013261.","DOI":"10.1530\/jrf.0.0170253"},{"key":"220","doi-asserted-by":"crossref","unstructured":"220. Scott JL, Ketheesan N, Summers PM. Spermatozoa and seminal plasma induce a greater inflammatory response in the ovine uterus at oestrus than dioestrus. Reprod Fertil Dev<\/i> 2009; 21: 817\u2013826.","DOI":"10.1071\/RD09012"},{"key":"221","doi-asserted-by":"crossref","unstructured":"221. Rickard JP, Warr S, de Graaf SP, Pini T. Ram sperm and seminal plasma alter immune transcriptome and cytokine secretion in ovine cervical explants ex vivo. Reproduction<\/i> 2025; 170: e250240.","DOI":"10.1530\/REP-25-0240"},{"key":"222","doi-asserted-by":"crossref","unstructured":"222. Warr S, Pini T, de Graaf SP, Rickard JP. Seminal plasma protects frozen-thawed ram spermatozoa from neutrophil attack: a complement mediated dynamic. Reproduction<\/i> 2025; 170: 170.","DOI":"10.1530\/REP-24-0465"},{"key":"223","doi-asserted-by":"crossref","unstructured":"223. Maxwell WM, Evans G, Mortimer ST, Gillan L, Gellatly ES, McPhie CA. Normal fertility in ewes after cervical insemination with frozen-thawed spermatozoa supplemented with seminal plasma. Reprod Fertil Dev<\/i> 1999; 11: 123\u2013126.","DOI":"10.1071\/RD99046"},{"key":"224","doi-asserted-by":"crossref","unstructured":"224. El-Hajj Ghaoui R, Thomson PC, Leahy T, Evans G, Maxwell WM. Autologous whole ram seminal plasma and its vesicle-free fraction improve motility characteristics and membrane status but not in vivo fertility of frozen-thawed ram spermatozoa. Reprod Domest Anim<\/i> 2007; 42: 541\u2013549.","DOI":"10.1111\/j.1439-0531.2006.00819.x"},{"key":"225","doi-asserted-by":"crossref","unstructured":"225. England GC, Burgess CM, Clutterbuck AL, Freeman SL. Epithelial surface changes and spermatozoa storage in the reproductive tract of the bitch. Vet J<\/i> 2013; 195: 185\u2013191.","DOI":"10.1016\/j.tvjl.2012.12.003"},{"key":"226","doi-asserted-by":"crossref","unstructured":"226. England GC, Russo M, Freeman SL. The bitch uterine response to semen deposition and its modification by male accessory gland secretions. Vet J<\/i> 2013; 195: 179\u2013184.","DOI":"10.1016\/j.tvjl.2012.04.027"},{"key":"227","doi-asserted-by":"crossref","unstructured":"227. Rijsselaere T, Van Soom A, Van Cruchten S, Coryn M, G\u00f6rtz K, Maes D, de Kruif A. Sperm distribution in the genital tract of the bitch following artificial insemination in relation to the time of ovulation. Reproduction<\/i> 2004; 128: 801\u2013811.","DOI":"10.1530\/rep.1.00273"},{"key":"228","doi-asserted-by":"crossref","unstructured":"228. Suarez SS. Regulation of sperm storage and movement in the mammalian oviduct. Int J Dev Biol<\/i> 2008; 52: 455\u2013462.","DOI":"10.1387\/ijdb.072527ss"},{"key":"229","doi-asserted-by":"crossref","unstructured":"229. N\u00f6thling JO, Shuttleworth R, de Haas K, Thompson PN. Homologous prostatic fluid added to frozen-thawed dog spermatozoa prior to intravaginal insemination of bitches resulted in better fertility than albumin-free TALP. Theriogenology<\/i> 2005; 64: 975\u2013991.","DOI":"10.1016\/j.theriogenology.2005.01.002"},{"key":"230","doi-asserted-by":"crossref","unstructured":"230. Marlin R, Nugeyre MT, Tchitchek N, Parenti M, Lefebvre C, Hocini H, Benjelloun F, Cannou C, Nozza S, Dereuddre-Bosquet N, Levy Y, Barr\u00e9-Sinoussi F, Scarlatti G, Le Grand R, Menu E. Seminal plasma exposures strengthen vaccine responses in the female reproductive tract mucosae. Front Immunol<\/i> 2019; 10: 430.","DOI":"10.3389\/fimmu.2019.00430"},{"key":"231","doi-asserted-by":"crossref","unstructured":"231. Nu\u00f1ez Favre R, Garc\u00eda MF, Ratto MH, Rearte R, Stornelli MC, de la Sota RL, Stornelli MA. Effect of cat seminal plasma and purified llama ovulation-inducing factor (\u03b2-NGF) on ovarian function in queens. Theriogenology<\/i> 2021; 169: 29\u201335.","DOI":"10.1016\/j.theriogenology.2021.04.008"},{"key":"232","doi-asserted-by":"crossref","unstructured":"232. Lockett NN, Scott VL, Boudreaux CE, Clay BT, Pruett SB, Ryan PL, Coats KS. Expression of regulatory T cell (Treg) activation markers in endometrial tissues from early and late pregnancy in the feline immunodeficiency virus (FIV)-infected cat. Placenta<\/i> 2010; 31: 796\u2013802.","DOI":"10.1016\/j.placenta.2010.06.019"},{"key":"233","doi-asserted-by":"crossref","unstructured":"233. Silva M, Fern\u00e1ndez A, Ulloa-Leal C, Adams GP, Berland MA, Ratto MH. LH release and ovulatory response after intramuscular, intravenous, and intrauterine administration of \u03b2-nerve growth factor of seminal plasma origin in female llamas. Theriogenology<\/i> 2015; 84: 1096\u20131102.","DOI":"10.1016\/j.theriogenology.2015.06.006"},{"key":"234","doi-asserted-by":"crossref","unstructured":"234. Urra F, Ratto MH, Silva M. Evaluation of the effect of mating, intrauterine deposition of raw seminal plasma or seminal plasma purified \u03b2-NGF on endometrial vascularization in llamas. Theriogenology<\/i> 2019; 125: 18\u201323.","DOI":"10.1016\/j.theriogenology.2018.10.007"},{"key":"235","doi-asserted-by":"crossref","unstructured":"235. Hidalgo AI, Ulloa-Leal C, Gajardo G, L\u00f3pez G, Carretta D, Burgos RA, Ratto M. Ovulation induced by intrauterine seminal plasma increases total protein, PGE2, IL-8, and IL-1\u03b2 in uterine fluid of Llamas (Lama glama<\/i>). Animals (Basel)<\/i> 2023; 13: 13.","DOI":"10.3390\/ani13040554"},{"key":"236","doi-asserted-by":"crossref","unstructured":"236. Koyanagi F, Nishiyama H. Fate of spermatozoa that do not participate in fertilization in the domestic fowl. Cell Tissue Res<\/i> 1981; 214: 89\u201395.","DOI":"10.1007\/BF00235147"},{"key":"237","doi-asserted-by":"crossref","unstructured":"237. Robertson SA. Immune regulation of conception and embryo implantation-all about quality control? J Reprod Immunol<\/i> 2010; 85: 51\u201357.","DOI":"10.1016\/j.jri.2010.01.008"},{"key":"238","doi-asserted-by":"crossref","unstructured":"238. Garratt M, Try H, Smiley KO, Grattan DR, Brooks RC. Mating in the absence of fertilization promotes a growth-reproduction versus lifespan trade-off in female mice. Proc Natl Acad Sci USA<\/i> 2020; 117: 15748\u201315754.","DOI":"10.1073\/pnas.2003159117"},{"key":"239","doi-asserted-by":"crossref","unstructured":"239. Chan HY, Schjenken JE, Sharkey DJ, Robertson SA. Assessing seminal fluid interaction with female reproductive tract tissues: in vivo and in vitro models for mouse. Methods Mol Biol<\/i> 2025; 2897: 649\u2013662.","DOI":"10.1007\/978-1-0716-4406-5_44"},{"key":"240","doi-asserted-by":"crossref","unstructured":"240. Song ZH, Li ZY, Li DD, Fang WN, Liu HY, Yang DD, Meng CY, Yang Y, Peng JP. Seminal plasma induces inflammation in the uterus through the \u03b3\u03b4 T\/IL-17 pathway. Sci Rep<\/i> 2016; 6: 25118.","DOI":"10.1038\/srep25118"},{"key":"241","doi-asserted-by":"crossref","unstructured":"241. Watkins AJ, Dias I, Tsuro H, Allen D, Emes RD, Moreton J, Wilson R, Ingram RJM, Sinclair KD. Paternal diet programs offspring health through sperm- and seminal plasma-specific pathways in mice. Proc Natl Acad Sci USA<\/i> 2018; 115: 10064\u201310069.","DOI":"10.1073\/pnas.1806333115"},{"key":"242","doi-asserted-by":"crossref","unstructured":"242. Ajdary M, Zandieh Z, Amjadi FS, Keyhanfar F, Mehdizadeh M, Aflatoonian R. Interaction of sperm with endometrium can regulate genes involved in endometrial receptivity pathway in mice: An experimental study. Int J Reprod Biomed (Yazd)<\/i> 2020; 18: 815\u2013824.","DOI":"10.18502\/ijrm.v13i10.7765"},{"key":"243","doi-asserted-by":"crossref","unstructured":"243. Wang D, Jueraitetibaike K, Tang T, Wang Y, Jing J, Xue T, Ma J, Cao S, Lin Y, Li X, Ma R, Chen X, Yao B. Seminal plasma and seminal plasma exosomes of aged male mice affect early embryo implantation via<\/i> immunomodulation. Front Immunol<\/i> 2021; 12: 723409.","DOI":"10.3389\/fimmu.2021.723409"},{"key":"244","doi-asserted-by":"crossref","unstructured":"244. Sanford TR, De M, Wood GW. Expression of colony-stimulating factors and inflammatory cytokines in the uterus of CD1 mice during days 1 to 3 of pregnancy. J Reprod Fertil<\/i> 1992; 94: 213\u2013220.","DOI":"10.1530\/jrf.0.0940213"},{"key":"245","doi-asserted-by":"crossref","unstructured":"245. Kim BJ, Choi YM, Rah SY, Park DR, Park SA, Chung YJ, Park SM, Park JK, Jang KY, Kim UH. Seminal CD38 is a pivotal regulator for fetomaternal tolerance. Proc Natl Acad Sci USA<\/i> 2015; 112: 1559\u20131564.","DOI":"10.1073\/pnas.1413493112"},{"key":"246","doi-asserted-by":"crossref","unstructured":"246. Denison FC, Grant VE, Calder AA, Kelly RW. Seminal plasma components stimulate interleukin-8 and interleukin-10 release. Mol Hum Reprod<\/i> 1999; 5: 220\u2013226.","DOI":"10.1093\/molehr\/5.3.220"},{"key":"247","doi-asserted-by":"crossref","unstructured":"247. Joseph T, Zalenskaya IA, Sawyer LC, Chandra N, Doncel GF. Seminal plasma induces prostaglandin-endoperoxide synthase (PTGS) 2 expression in immortalized human vaginal cells: involvement of semen prostaglandin E2 in PTGS2 upregulation. Biol Reprod<\/i> 2013; 88: 13.","DOI":"10.1095\/biolreprod.112.101956"},{"key":"248","doi-asserted-by":"crossref","unstructured":"248. Introini A, Bostr\u00f6m S, Bradley F, Gibbs A, Glaessgen A, Tjernlund A, Broliden K. Seminal plasma induces inflammation and enhances HIV-1 replication in human cervical tissue explants. PLoS Pathog<\/i> 2017; 13: e1006402.","DOI":"10.1371\/journal.ppat.1006402"},{"key":"249","doi-asserted-by":"crossref","unstructured":"249. Martin JW, Chen JC, Neidleman J, Tatsumi K, Hu J, Giudice LC, Greene WC, Roan NR. Potent and rapid activation of tropomyosin-receptor kinase A in endometrial stromal fibroblasts by seminal plasma. Biol Reprod<\/i> 2018; 99: 336\u2013348.","DOI":"10.1093\/biolre\/ioy056"},{"key":"250","doi-asserted-by":"crossref","unstructured":"250. Ibrahim MG, Elghonaimy EA, Sch\u00e4fer S, Vennemann M, Kliesch S, Kiesel L, G\u00f6tte M, Sch\u00fcring AN. Seminal plasma (SP) induces a rapid transforming growth factor beta 1 (TGF\u03b21)-independent up-regulation of epithelial-mesenchymal transdifferentiation (EMT) and myofibroblastic metaplasia-markers in endometriotic (EM) and endometrial cells. Arch Gynecol Obstet<\/i> 2019; 299: 173\u2013183.","DOI":"10.1007\/s00404-018-4965-4"},{"key":"251","doi-asserted-by":"crossref","unstructured":"251. Rodriguez-Caro H, Dragovic R, Shen M, Dombi E, Mounce G, Field K, Meadows J, Turner K, Lunn D, Child T, Southcombe JH, Granne I. In vitro<\/i> decidualisation of human endometrial stromal cells is enhanced by seminal fluid extracellular vesicles. J Extracell Vesicles<\/i> 2019; 8: 1565262.","DOI":"10.1080\/20013078.2019.1565262"},{"key":"252","doi-asserted-by":"crossref","unstructured":"252. Paktinat S, Hashemi SM, Ghaffari Novin M, Mohammadi-Yeganeh S, Salehpour S, Karamian A, Nazarian H. Seminal exosomes induce interleukin-6 and interleukin-8 secretion by human endometrial stromal cells. Eur J Obstet Gynecol Reprod Biol<\/i> 2019; 235: 71\u201376.","DOI":"10.1016\/j.ejogrb.2019.02.010"},{"key":"253","doi-asserted-by":"crossref","unstructured":"253. George AF, Jang KS, Nyegaard M, Neidleman J, Spitzer TL, Xie G, Chen JC, Herzig E, Laustsen A, Marques de Menezes EG, Houshdaran S, Pilcher CD, Norris PJ, Jakobsen MR, Greene WC, Giudice LC, Roan NR. Seminal plasma promotes decidualization of endometrial stromal fibroblasts in vitro from women with and without inflammatory disorders in a manner dependent on interleukin-11 signaling. Hum Reprod<\/i> 2020; 35: 617\u2013640.","DOI":"10.1093\/humrep\/deaa015"},{"key":"254","unstructured":"254. Moharrami T, Ai J, Ebrahimi-Barough S, Nouri M, Ziadi M, Pashaiefar H, Yazarlou F, Ahmadvand M, Najafi S, Modarressi MH. Influence of follicular fluid and seminal plasma on the expression of endometrial receptivity genes in endometrial cells. Cell J<\/i> 2021; 22: 457\u2013466."},{"key":"255","doi-asserted-by":"crossref","unstructured":"255. Paktinat S, Esfandyari S, Karamian A, Koochaki A, Asadirad A, Ghaffari Novin M, Mohammadi-Yeganeh S, Salehpour S, Hashemi SM, Nazarian H. Conditioned medium derived from seminal extracellular vesicles-exposed endometrial stromal cells induces inflammatory cytokine secretion by macrophages. Eur J Obstet Gynecol Reprod Biol<\/i> 2021; 262: 174\u2013181.","DOI":"10.1016\/j.ejogrb.2021.05.019"},{"key":"256","doi-asserted-by":"crossref","unstructured":"256. Wang H, Lin Y, Chen R, Zhu Y, Wang H, Li S, Yu L, Zhang K, Liu Y, Jing T, Sun F. Human seminal extracellular vesicles enhance endometrial receptivity through leukemia inhibitory factor. Endocrinology<\/i> 2024; 165: bqae035.","DOI":"10.1210\/endocr\/bqae035"},{"key":"257","doi-asserted-by":"crossref","unstructured":"257. Liu L, Liu C, Lou F, Zhang G, Wang X, Fan Y, Yan K, Wang K, Xu Z, Hu S, Bj\u00f6rkholm M, Xu D. Activation of telomerase by seminal plasma in malignant and normal cervical epithelial cells. J Pathol<\/i> 2011; 225: 203\u2013211.","DOI":"10.1002\/path.2914"},{"key":"258","doi-asserted-by":"crossref","unstructured":"258. Zhang Y, Chen X, Li J, Chen X, Zhao J, Liu Q, Li X, Wang X, Xiao Z. Seminal plasma exosome derived miR-26-5p can regulate decidual macrophage polarization via PTEN \/ PI3K \/ AKT signaling pathway. Sci Rep<\/i> 2025; 15: 9192.","DOI":"10.1038\/s41598-025-92880-2"},{"key":"259","doi-asserted-by":"crossref","unstructured":"259. Schieve LA, Meikle SF, Ferre C, Peterson HB, Jeng G, Wilcox LS. Low and very low birth weight in infants conceived with use of assisted reproductive technology. N Engl J Med<\/i> 2002; 346: 731\u2013737.","DOI":"10.1056\/NEJMoa010806"},{"key":"260","doi-asserted-by":"crossref","unstructured":"260. Ceelen M, van Weissenbruch MM, Roos JC, Vermeiden JP, van Leeuwen FE, Delemarre-van de Waal HA. Body composition in children and adolescents born after in vitro fertilization or spontaneous conception. J Clin Endocrinol Metab<\/i> 2007; 92: 3417\u20133423.","DOI":"10.1210\/jc.2006-2896"},{"key":"261","doi-asserted-by":"crossref","unstructured":"261. Ceelen M, van Weissenbruch MM, Vermeiden JP, van Leeuwen FE, Delemarre-van de Waal HA. Cardiometabolic differences in children born after in vitro fertilization: follow-up study. J Clin Endocrinol Metab<\/i> 2008; 93: 1682\u20131688.","DOI":"10.1210\/jc.2007-2432"},{"key":"262","doi-asserted-by":"crossref","unstructured":"262. Alvarez-Rodriguez M, Atikuzzaman M, Venhoranta H, Wright D, Rodriguez-Martinez H. Expression of immune regulatory genes in the porcine internal genital tract is differentially triggered by spermatozoa and seminal plasma. Int J Mol Sci<\/i> 2019; 20: 513.","DOI":"10.3390\/ijms20030513"},{"key":"263","doi-asserted-by":"crossref","unstructured":"263. Alvarez-Rodriguez M, Martinez CA, Wright D, Rodriguez-Martinez H. The role of semen and seminal plasma in inducing large-scale genomic changes in the female porcine peri-ovulatory tract. Sci Rep<\/i> 2020; 10: 5061.","DOI":"10.1038\/s41598-020-60810-z"},{"key":"264","doi-asserted-by":"crossref","unstructured":"264. Rozeboom KJ, Troedsson MH, Molitor TW, Crabo BG. The effect of spermatozoa and seminal plasma on leukocyte migration into the uterus of gilts. J Anim Sci<\/i> 1999; 77: 2201\u20132206.","DOI":"10.2527\/1999.7782201x"},{"key":"265","doi-asserted-by":"crossref","unstructured":"265. Nash DM, Sheldon IM, Herath S, Lane EA. Endometrial explant culture to study the response of equine endometrium to insemination. Reprod Domest Anim<\/i> 2010; 45: 670\u2013676.","DOI":"10.1111\/j.1439-0531.2008.01328.x"},{"key":"266","doi-asserted-by":"crossref","unstructured":"266. Nongbua T, Guo Y, Ntallaris T, Rub\u00e9r M, Rodriguez-Martinez H, Humblot P, Morrell JM. Bull seminal plasma stimulates in vitro production of TGF-\u03b2, IL-6 and IL-8 from bovine endometrial epithelial cells, depending on dose and bull fertility. J Reprod Immunol<\/i> 2020; 142: 103179.","DOI":"10.1016\/j.jri.2020.103179"},{"key":"267","doi-asserted-by":"crossref","unstructured":"267. Scott JL, Ketheesan N, Summers PM. Leucocyte population changes in the reproductive tract of the ewe in response to insemination. Reprod Fertil Dev<\/i> 2006; 18: 627\u2013634.","DOI":"10.1071\/RD05165"},{"key":"268","doi-asserted-by":"crossref","unstructured":"268. Li X, Zhao X. Separation and purification of ovulation-inducing factors in the seminal plasma of the Bactrian camel (Camelus bactrianus). Vet Res Commun<\/i> 2004; 28: 235\u2013245.","DOI":"10.1023\/B:VERC.0000017370.74401.be"},{"key":"269","doi-asserted-by":"crossref","unstructured":"269. Ratto MH, Huanca W, Singh J, Adams GP. Local versus systemic effect of ovulation-inducing factor in the seminal plasma of alpacas. Reprod Biol Endocrinol<\/i> 2005; 3: 29.","DOI":"10.1186\/1477-7827-3-29"}],"container-title":["Journal of Reproduction and Development"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.jstage.jst.go.jp\/article\/jrd\/72\/3\/72_2026-013\/_pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,6,20]],"date-time":"2026-06-20T03:27:49Z","timestamp":1781926069000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.jstage.jst.go.jp\/article\/jrd\/72\/3\/72_2026-013\/_article"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026]]},"references-count":269,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2026]]}},"URL":"https:\/\/doi.org\/10.1262\/jrd.2026-013","relation":{},"ISSN":["0916-8818","1348-4400"],"issn-type":[{"value":"0916-8818","type":"print"},{"value":"1348-4400","type":"electronic"}],"subject":[],"published":{"date-parts":[[2026]]},"article-number":"2026-013"}}