<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(1)</volume><submitter>Mountain KE</submitter><funding>Wellcome Trust</funding><pubmed_abstract>The mechanisms by which vaginal microbiota shape spontaneous preterm birth (sPTB) risk remain poorly defined. Using electronic clinical records data from 74,913 maternities in conjunction with metaxanomic (n = 596) and immune profiling (n = 314) data, we show that the B blood group phenotype associates with increased risk of sPTB and adverse vaginal microbiota composition. The O blood group associates with sPTB in women who have a combination of a previous history of sPTB, an adverse vaginal microbial composition and pro-inflammatory cervicovaginal milieu. In contrast, women of blood group A have a higher prevalence of vaginal Lactobacillus crispatus, a lower risk of sPTB, with sPTB cases showing no association with vaginal microbiota composition or inflammation. We found that cervicovagin</pubmed_abstract><journal>NPJ biofilms and microbiomes</journal><pagination>170</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12423329</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>ABO blood group antigens influence host-microbe interactions and risk of early spontaneous preterm birth.</pubmed_title><pmcid>PMC12423329</pmcid><pubmed_authors>Tajadura-Ortega V</pubmed_authors><pubmed_authors>Hyde AKC</pubmed_authors><pubmed_authors>Brown RG</pubmed_authors><pubmed_authors>Feizi T</pubmed_authors><pubmed_authors>Glampson B</pubmed_authors><pubmed_authors>Dell A</pubmed_authors><pubmed_authors>Grassi P</pubmed_authors><pubmed_authors>Mayer E</pubmed_authors><pubmed_authors>Wu G</pubmed_authors><pubmed_authors>Sykes L</pubmed_authors><pubmed_authors>Haslam SM</pubmed_authors><pubmed_authors>Bennett PR</pubmed_authors><pubmed_authors>Mountain KE</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Pasint-Magyar J</pubmed_authors><pubmed_authors>Teoh TG</pubmed_authors><pubmed_authors>Chai W</pubmed_authors><pubmed_authors>Lee YS</pubmed_authors><pubmed_authors>Marchesi JR</pubmed_authors><pubmed_authors>Stock SJ</pubmed_authors><pubmed_authors>Green A</pubmed_authors><pubmed_authors>Ng S</pubmed_authors><pubmed_authors>Terzidou V</pubmed_authors><pubmed_authors>David AL</pubmed_authors><pubmed_authors>Chan D</pubmed_authors><pubmed_authors>Gimeno-Molina B</pubmed_authors><pubmed_authors>MacIntyre DA</pubmed_authors><pubmed_authors>Lewis HV</pubmed_authors><pubmed_authors>Roberts LA</pubmed_authors><pubmed_authors>Norman JE</pubmed_authors><pubmed_authors>Kundu S</pubmed_authors></additional><is_claimable>false</is_claimable><name>ABO blood group antigens influence host-microbe interactions and risk of early spontaneous preterm birth.</name><description>The mechanisms by which vaginal microbiota shape spontaneous preterm birth (sPTB) risk remain poorly defined. Using electronic clinical records data from 74,913 maternities in conjunction with metaxanomic (n = 596) and immune profiling (n = 314) data, we show that the B blood group phenotype associates with increased risk of sPTB and adverse vaginal microbiota composition. The O blood group associates with sPTB in women who have a combination of a previous history of sPTB, an adverse vaginal microbial composition and pro-inflammatory cervicovaginal milieu. In contrast, women of blood group A have a higher prevalence of vaginal Lactobacillus crispatus, a lower risk of sPTB, with sPTB cases showing no association with vaginal microbiota composition or inflammation. We found that cervicovagin</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-03T07:43:33.251Z</modification><creation>2026-04-26T03:09:39.82Z</creation></dates><accession>S-EPMC12423329</accession><cross_references><pubmed>40931094</pubmed><doi>10.1038/s41522-025-00783-x</doi></cross_references></HashMap>