{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T11:01:06Z","timestamp":1791284466978,"version":"4.1.0"},"reference-count":44,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2017,5,4]],"date-time":"2017-05-04T00:00:00Z","timestamp":1493856000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100000268","name":"Biotechnology and Biological Sciences Research Council","doi-asserted-by":"publisher","award":["BB\/J004227\/1"],"award-info":[{"award-number":["BB\/J004227\/1"]}],"id":[{"id":"10.13039\/501100000268","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100000268","name":"Biotechnology and Biological Sciences Research Council","doi-asserted-by":"publisher","award":["BB\/L007452\/1"],"award-info":[{"award-number":["BB\/L007452\/1"]}],"id":[{"id":"10.13039\/501100000268","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Immunology"],"published-print":{"date-parts":[[2017,7]]},"abstract":"<jats:title>Summary<\/jats:title>\n                  <jats:p>\n                    Marginal zone (\n                    <jats:styled-content style=\"fixed-case\">MZ<\/jats:styled-content>\n                    ) B cells are positioned within the spleen to capture blood\u2010borne antigen and immune complexes and deliver them to follicular dendritic cells in the B\u2010cell follicles. We show that within the spleens of aged mice antigen capture by\n                    <jats:styled-content style=\"fixed-case\">MZ<\/jats:styled-content>\n                    B cells, and their ability to shuttle between the follicle and\n                    <jats:styled-content style=\"fixed-case\">MZ<\/jats:styled-content>\n                    , were impaired. The ability of aged\n                    <jats:styled-content style=\"fixed-case\">MZ<\/jats:styled-content>\n                    B cells to migrate towards the\n                    <jats:styled-content style=\"fixed-case\">MZ<\/jats:styled-content>\n                    chemoattractant sphingosine\u20101\u2010phosphate was increased, suggesting that aged\n                    <jats:styled-content style=\"fixed-case\">MZ<\/jats:styled-content>\n                    B cells had a greater propensity to be retained within the\n                    <jats:styled-content style=\"fixed-case\">MZ<\/jats:styled-content>\n                    . An extrinsic impairment in aged B\u2010cell migration towards the\n                    <jats:styled-content style=\"fixed-case\">MZ<\/jats:styled-content>\n                    was demonstrated using bone marrow chimeras. The follicular shuttling of\n                    <jats:styled-content style=\"fixed-case\">MZ<\/jats:styled-content>\n                    B cells derived from either young or aged bone marrow was similarly reduced in aged recipient spleens, showing that ageing effects on splenic stromal cells were responsible for the impaired follicular shuttling of\n                    <jats:styled-content style=\"fixed-case\">MZ<\/jats:styled-content>\n                    B cells.\n                    <jats:styled-content style=\"fixed-case\">MZ<\/jats:styled-content>\n                    B cells rapidly mount T\u2010cell\u2010independent (\n                    <jats:styled-content style=\"fixed-case\">TI<\/jats:styled-content>\n                    ) antibody\u2010responses to microbial polysaccharide antigen. In aged mice the ability to produce immunoglobulins in response to the\n                    <jats:styled-content style=\"fixed-case\">TI<\/jats:styled-content>\n                    type 1 antigen\n                    <jats:styled-content style=\"fixed-case\">TNP<\/jats:styled-content>\n                    \u2010\n                    <jats:styled-content style=\"fixed-case\">LPS<\/jats:styled-content>\n                    was impaired. These ageing\u2010related changes to the\n                    <jats:styled-content style=\"fixed-case\">MZ<\/jats:styled-content>\n                    and\n                    <jats:styled-content style=\"fixed-case\">MZ<\/jats:styled-content>\n                    B cells have implications for the clearance of blood\u2010borne pathogens. Indeed elderly people have increased susceptibility to\n                    <jats:italic>Streptococcus pneumoniae<\/jats:italic>\n                    , a\n                    <jats:styled-content style=\"fixed-case\">TI<\/jats:styled-content>\n                    antigen, and decreased responses to vaccination. A thorough analysis of the mechanisms that underpin the ageing\u2010related decline in the status of the\n                    <jats:styled-content style=\"fixed-case\">MZ<\/jats:styled-content>\n                    and\n                    <jats:styled-content style=\"fixed-case\">MZ<\/jats:styled-content>\n                    B cells will help the design of novel treatments to improve immunity in the elderly.\n                  <\/jats:p>","DOI":"10.1111\/imm.12737","type":"journal-article","created":{"date-parts":[[2017,4,4]],"date-time":"2017-04-04T20:39:54Z","timestamp":1491338394000},"page":"349-362","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":51,"title":["Ageing adversely affects the migration and function of marginal zone B cells"],"prefix":"10.1111","volume":"151","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2013-2559","authenticated-orcid":false,"given":"Vivian M.","family":"Turner","sequence":"first","affiliation":[{"name":"The Roslin Institute and Royal (Dick) School of Veterinary Sciences University of Edinburgh Midlothian UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7395-1796","authenticated-orcid":false,"given":"Neil A.","family":"Mabbott","sequence":"additional","affiliation":[{"name":"The Roslin Institute and Royal (Dick) School of Veterinary Sciences University of Edinburgh Midlothian UK"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2017,5,4]]},"reference":[{"key":"e_1_2_9_2_1","doi-asserted-by":"publisher","DOI":"10.1146\/annurev.immunol.23.021704.115728"},{"key":"e_1_2_9_3_1","doi-asserted-by":"publisher","DOI":"10.1038\/ni1083"},{"key":"e_1_2_9_4_1","doi-asserted-by":"publisher","DOI":"10.1038\/ni1542"},{"key":"e_1_2_9_5_1","doi-asserted-by":"publisher","DOI":"10.1093\/intimm\/dxh142"},{"key":"e_1_2_9_6_1","doi-asserted-by":"publisher","DOI":"10.1126\/science.290.5489.89"},{"key":"e_1_2_9_7_1","doi-asserted-by":"publisher","DOI":"10.1128\/JVI.05581-11"},{"key":"e_1_2_9_8_1","doi-asserted-by":"publisher","DOI":"10.1099\/vir.0.058958-0"},{"key":"e_1_2_9_9_1","doi-asserted-by":"publisher","DOI":"10.4049\/jimmunol.1001271"},{"key":"e_1_2_9_10_1","doi-asserted-by":"publisher","DOI":"10.1111\/imm.12590"},{"key":"e_1_2_9_11_1","doi-asserted-by":"publisher","DOI":"10.4049\/jimmunol.175.12.8173"},{"key":"e_1_2_9_12_1","doi-asserted-by":"publisher","DOI":"10.1089\/hyb.2010.0093"},{"key":"e_1_2_9_13_1","doi-asserted-by":"crossref","first-page":"3200","DOI":"10.4049\/jimmunol.143.10.3200","article-title":"Immaturity of the human splenic marginal zone in infancy. 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