{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,21]],"date-time":"2026-10-21T00:38:22Z","timestamp":1792543102941,"version":"4.5.0"},"reference-count":25,"publisher":"Wiley","license":[{"start":{"date-parts":[[2026,10,20]],"date-time":"2026-10-20T00:00:00Z","timestamp":1792454400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2026,10,20]],"date-time":"2026-10-20T00:00:00Z","timestamp":1792454400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Vox Sanguinis"],"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background and Objectives<\/jats:title>\n                    <jats:p>\n                      To characterise\n                      <jats:italic>FUT2<\/jats:italic>\n                      and\n                      <jats:italic>FUT3<\/jats:italic>\n                      haplotype and genotype frequencies among 529 Shanghai Han voluntary blood donors, and quantify erythrocyte Le\u1d43 and Le\u1d47 expression via flow cytometry. This study extends the established\n                      <jats:italic>Se\u02b7<\/jats:italic>\n                      \/c.418A&gt;T partial\u2010secretor model to a large Chinese cohort using combined sequencing and quantitative red cell Lewis antigen flow cytometry.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Materials and Methods<\/jats:title>\n                    <jats:p>\n                      Routine serological ABO grouping was performed. Flow cytometry was used to quantify Le\u1d43 and Le\u1d47 mean fluorescence intensity (MFI). Sanger sequencing combined with thymine\u2013adenine (TA) cloning was applied to resolve\n                      <jats:italic>FUT2<\/jats:italic>\n                      \/\n                      <jats:italic>FUT3<\/jats:italic>\n                      cis\u2010haplotypes. Owing to marked skewness and heteroscedasticity of MFI data, non\u2010parametric Mann\u2013Whitney\n                      <jats:italic>U<\/jats:italic>\n                      tests with Bonferroni correction were used for subgroup comparisons.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      A total of 1046\n                      <jats:italic>FUT2<\/jats:italic>\n                      alleles were genotyped: secretor (\n                      <jats:italic>Se<\/jats:italic>\n                      ,\n                      <jats:italic>n<\/jats:italic>\n                      \u2009=\u2009575, 54.3%), weak\u2010secretor (\n                      <jats:italic>Se\u02b7<\/jats:italic>\n                      ,\n                      <jats:italic>n<\/jats:italic>\n                      \u2009=\u2009443, 41.9%), non\u2010secretor (\n                      <jats:italic>se<\/jats:italic>\n                      ,\n                      <jats:italic>n<\/jats:italic>\n                      \u2009=\u200928, 2.6%), with eight novel sequence variants. For\n                      <jats:italic>FUT3<\/jats:italic>\n                      , 1053 alleles were resolved: functional (\n                      <jats:italic>Le<\/jats:italic>\n                      ,\n                      <jats:italic>n<\/jats:italic>\n                      \u2009=\u2009806, 76.2%), loss\u2010of\u2010function (\n                      <jats:italic>le<\/jats:italic>\n                      ,\n                      <jats:italic>n<\/jats:italic>\n                      \u2009=\u2009247, 23.3%), alongside five novel variants (0.5%).\n                      <jats:italic>Se\u02b7<\/jats:italic>\n                      homozygosity elevated Le\u1d43 and reduced Le\u1d47 in carriers with functional\n                      <jats:italic>FUT3<\/jats:italic>\n                      . Considerable inter\u2010individual variability persisted even among donors with identical\n                      <jats:italic>ABO<\/jats:italic>\n                      \u2013\n                      <jats:italic>FUT2<\/jats:italic>\n                      \u2013\n                      <jats:italic>FUT3<\/jats:italic>\n                      genotypes.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      Erythrocyte Lewis antigen abundance is primarily governed by competitive substrate utilisation of a common type 1 precursor glycan by\n                      <jats:italic>FUT2<\/jats:italic>\n                      and\n                      <jats:italic>FUT3<\/jats:italic>\n                      glycosyltransferases. The residual heterogeneity indicates additional host factors beyond these three loci. This study validates the classic\n                      <jats:italic>Se\u02b7<\/jats:italic>\n                      partial\u2010secretor model in a Chinese cohort and provides population reference data, rather than reporting unrecognised biosynthetic pathways.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/vox.70383","type":"journal-article","created":{"date-parts":[[2026,10,20]],"date-time":"2026-10-20T23:51:21Z","timestamp":1792540281000},"source":"Crossref","is-referenced-by-count":0,"title":["Comprehensive analysis of Lewis antigen expression patterns in a Chinese blood donor cohort"],"prefix":"10.1111","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-8347-0355","authenticated-orcid":false,"given":"Jiewei","family":"Zheng","sequence":"first","affiliation":[{"name":"Blood Group Reference Laboratory, Institute of Blood Transfusion Shanghai Blood Center  Shanghai China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yuyu","family":"Zhang","sequence":"additional","affiliation":[{"name":"Blood Group Reference Laboratory, Institute of Blood Transfusion Shanghai Blood Center  Shanghai China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sha","family":"Jin","sequence":"additional","affiliation":[{"name":"Blood Group Reference Laboratory, Institute of Blood Transfusion Shanghai Blood Center  Shanghai China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xinyi","family":"Zhu","sequence":"additional","affiliation":[{"name":"Blood Group Reference Laboratory, Institute of Blood Transfusion Shanghai Blood Center  Shanghai China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dong","family":"Xiang","sequence":"additional","affiliation":[{"name":"Blood Group Reference Laboratory, Institute of Blood Transfusion Shanghai Blood Center  Shanghai China"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2026,10,20]]},"reference":[{"key":"e_1_2_9_2_1","first-page":"198","volume-title":"Immunohematology","author":"Liu DZ","year":"2002"},{"key":"e_1_2_9_3_1","doi-asserted-by":"crossref","first-page":"4632","DOI":"10.1074\/jbc.270.9.4632","article-title":"Molecular cloning of a human genomic region containing the H blood group \u03b1(1,2)\u2010fucosyltransferase gene and two H locus\u2010related DNA restriction fragments","volume":"270","author":"Rouquier S","year":"1995","journal-title":"J Biol Chem"},{"key":"e_1_2_9_4_1","first-page":"947","article-title":"Preliminary study on salivary ABO blood group substances and FUT2\/FUT3 gene polymorphisms in Chinese population","volume":"9","author":"Jin S","year":"2018","journal-title":"Chin J Blood Transfus"},{"key":"e_1_2_9_5_1","doi-asserted-by":"crossref","first-page":"51","DOI":"10.21307\/immunohematology-2019-746","article-title":"Review: phenotyping for Lewis and secretor histo\u2010blood group antigens","volume":"12","author":"Henry SM","year":"1996","journal-title":"Immunohematology"},{"key":"e_1_2_9_6_1","doi-asserted-by":"crossref","first-page":"9830","DOI":"10.1074\/jbc.271.16.9830","article-title":"Molecular genetic analysis of the human Lewis histo\u2010blood group system. 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Evidence of a weak secretor phenotype","volume":"58","author":"Henry SM","year":"1990","journal-title":"Vox Sang"},{"key":"e_1_2_9_15_1","first-page":"62","article-title":"Plasma and red cell glycolipid patterns of Le(a+b+) and Le(a+b\u2212) Polynesians as further evidence of the weak secretor gene, Se\u02b7","volume":"65","author":"Henry SM","year":"1993","journal-title":"Vox Sang"},{"key":"e_1_2_9_16_1","doi-asserted-by":"crossref","first-page":"675","DOI":"10.1006\/bbrc.1996.0293","article-title":"Homozygous expression of a missense mutation at nucleotide 385 in the FUT2 gene associates with the Le(a+b+) partial\u2010secretor phenotype in an Indonesian family","volume":"219","author":"Henry SM","year":"1996","journal-title":"Biochem Biophys Res Commun"},{"key":"e_1_2_9_17_1","doi-asserted-by":"crossref","first-page":"329","DOI":"10.1042\/bj3120329","article-title":"Correlation of a missense mutation in the human secretor \u03b1(1,2)\u2010fucosyltransferase gene with the Lewis(a+b+) phenotype: a potential molecular basis for the weak secretor allele, Se\u02b7","volume":"312","author":"Yu LC","year":"1995","journal-title":"Biochem J"},{"key":"e_1_2_9_18_1","first-page":"343","article-title":"Molecular basis for secretor type \u03b1(1,2)\u2010fucosyltransferase gene deficiency in a Japanese population","volume":"59","author":"Koda Y","year":"1996","journal-title":"Am J Hum Genet"},{"key":"e_1_2_9_19_1","doi-asserted-by":"crossref","first-page":"325","DOI":"10.1111\/trf.13384","article-title":"Glycomapping the fine specificity of monoclonal and polyclonal Lewis antibodies with type\u2010specific kodecytes and FSL constructs on paper","volume":"56","author":"Williams E","year":"2016","journal-title":"Transfusion"},{"key":"e_1_2_9_20_1","doi-asserted-by":"crossref","first-page":"4640","DOI":"10.1074\/jbc.270.9.4640","article-title":"Sequence and expression of a candidate for the human secretor blood group \u03b1(1,2)\u2010fucosyltransferase gene (FUT2). 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