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

IF 3.7 3区 医学 Q2 IMMUNOLOGY
Marleen Y. van Smoorenburg, Julia L. Nerwinska, John L. van Hamme, Ester B. M. Remmerswaal, Celia Segui-Perez, Karin Strijbis, Teunis B. H. Geijtenbeek
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引用次数: 0

摘要

阴道微生物群失调与女性生殖道炎症增加有关。与细菌性阴道病(BV)相关的微生物群,如阴道加德纳菌、elsdenmegasphaera和timonprevotella,取代了与健康相关的细菌crispatus乳杆菌,引起炎症,影响粘膜完整性和免疫力。然而,目前尚不清楚这些bv相关细菌如何调节免疫细胞并增强炎症。在这里,我们研究了bv相关细菌是否直接影响树突状细胞(DC)的功能。值得注意的是,P. timonensis而不是M. elsdenii诱导单核细胞系之间的细胞聚集,重要的是,在原代DCs和原代CD4 T细胞之间。我们的数据表明,这种增加的聚类与LFA-1无关。此外,提蒙假单胞菌可增强dc介导的CD4 T细胞增殖。总之,这些结果表明,P. timonensis诱导的细胞-细胞聚集有助于细菌性阴道病期间观察到的粘膜炎症升高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Bacterial Vaginosis-Associated Prevotella timonensis Enhances Dendritic Cell–T Cell Clustering and Subsequent T Cell Proliferation

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.

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来源期刊
CiteScore
8.30
自引率
3.70%
发文量
224
审稿时长
2 months
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.
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