Marleen Y. van Smoorenburg, Julia L. Nerwinska, John L. van Hamme, Ester B. M. Remmerswaal, Celia Segui-Perez, Karin Strijbis, Teunis B. H. Geijtenbeek
{"title":"细菌性阴道病相关的蒙古普氏菌增强树突状细胞- T细胞聚集和随后的T细胞增殖","authors":"Marleen Y. van Smoorenburg, Julia L. Nerwinska, John L. van Hamme, Ester B. M. Remmerswaal, Celia Segui-Perez, Karin Strijbis, Teunis B. H. Geijtenbeek","doi":"10.1002/eji.70051","DOIUrl":null,"url":null,"abstract":"<p>Dysbiosis of the vaginal microbiome is associated with increased inflammation in the female genital tract. Microbiota associated with bacterial vaginosis (BV), such as <i>Gardnerella vaginalis</i>, <i>Megasphaera elsdenii</i>, and <i>Prevotella timonensis</i>, replace the health-associated bacterium <i>Lactobacillus crispatus</i> and cause inflammation affecting mucosal integrity and immunity. However, it remains unclear how these BV-associated bacteria modulate immune cells and enhance inflammation. Here, we investigated whether BV-associated bacteria directly affected dendritic cell (DC) function. Notably, <i>P. timonensis</i> but not <i>M. elsdenii</i> induced cell–cell clustering between monocytic cell lines and, importantly, between primary DCs and primary CD4 T cells. Our data indicate that this increased clustering is independent of LFA-1. Moreover, <i>P. timonensis</i> enhanced DC-mediated CD4 T cell proliferation. Altogether, these results suggest that <i>P. timonensis</i>-induced cell–cell clustering contributes to the elevated mucosal inflammation observed during bacterial vaginosis.</p>","PeriodicalId":165,"journal":{"name":"European Journal of Immunology","volume":"55 9","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2025-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/eji.70051","citationCount":"0","resultStr":"{\"title\":\"Bacterial Vaginosis-Associated Prevotella timonensis Enhances Dendritic Cell–T Cell Clustering and Subsequent T Cell Proliferation\",\"authors\":\"Marleen Y. van Smoorenburg, Julia L. Nerwinska, John L. van Hamme, Ester B. M. Remmerswaal, Celia Segui-Perez, Karin Strijbis, Teunis B. H. Geijtenbeek\",\"doi\":\"10.1002/eji.70051\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Dysbiosis of the vaginal microbiome is associated with increased inflammation in the female genital tract. Microbiota associated with bacterial vaginosis (BV), such as <i>Gardnerella vaginalis</i>, <i>Megasphaera elsdenii</i>, and <i>Prevotella timonensis</i>, replace the health-associated bacterium <i>Lactobacillus crispatus</i> and cause inflammation affecting mucosal integrity and immunity. However, it remains unclear how these BV-associated bacteria modulate immune cells and enhance inflammation. Here, we investigated whether BV-associated bacteria directly affected dendritic cell (DC) function. Notably, <i>P. timonensis</i> but not <i>M. elsdenii</i> induced cell–cell clustering between monocytic cell lines and, importantly, between primary DCs and primary CD4 T cells. Our data indicate that this increased clustering is independent of LFA-1. Moreover, <i>P. timonensis</i> enhanced DC-mediated CD4 T cell proliferation. Altogether, these results suggest that <i>P. timonensis</i>-induced cell–cell clustering contributes to the elevated mucosal inflammation observed during bacterial vaginosis.</p>\",\"PeriodicalId\":165,\"journal\":{\"name\":\"European Journal of Immunology\",\"volume\":\"55 9\",\"pages\":\"\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-09-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/eji.70051\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European Journal of Immunology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/eji.70051\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Immunology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/eji.70051","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
Bacterial Vaginosis-Associated Prevotella timonensis Enhances Dendritic Cell–T Cell Clustering and Subsequent T Cell Proliferation
Dysbiosis of the vaginal microbiome is associated with increased inflammation in the female genital tract. Microbiota associated with bacterial vaginosis (BV), such as Gardnerella vaginalis, Megasphaera elsdenii, and Prevotella timonensis, replace the health-associated bacterium Lactobacillus crispatus and cause inflammation affecting mucosal integrity and immunity. However, it remains unclear how these BV-associated bacteria modulate immune cells and enhance inflammation. Here, we investigated whether BV-associated bacteria directly affected dendritic cell (DC) function. Notably, P. timonensis but not M. elsdenii induced cell–cell clustering between monocytic cell lines and, importantly, between primary DCs and primary CD4 T cells. Our data indicate that this increased clustering is independent of LFA-1. Moreover, P. timonensis enhanced DC-mediated CD4 T cell proliferation. Altogether, these results suggest that P. timonensis-induced cell–cell clustering contributes to the elevated mucosal inflammation observed during bacterial vaginosis.
期刊介绍:
The European Journal of Immunology (EJI) is an official journal of EFIS. Established in 1971, EJI continues to serve the needs of the global immunology community covering basic, translational and clinical research, ranging from adaptive and innate immunity through to vaccines and immunotherapy, cancer, autoimmunity, allergy and more. Mechanistic insights and thought-provoking immunological findings are of interest, as are studies using the latest omics technologies. We offer fast track review for competitive situations, including recently scooped papers, format free submission, transparent and fair peer review and more as detailed in our policies.