阴道提蒙普氏菌增强HIV-1摄取并通过不同的初级树突状细胞亚群差异影响传播

IF 4.5 3区 医学 Q2 IMMUNOLOGY
Marleen Y. van Smoorenburg, Ester B. M. Remmerswaal, Celia Segui-Perez, John L. van Hamme, Karin Strijbis, Teunis B. H. Geijtenbeek
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引用次数: 0

摘要

年轻女性感染HIV-1的风险很高,阴道微生物群的不平衡增加了对HIV-1感染的易感性。对潜在机制的更多了解可能会为预防HIV-1感染和传播开辟新的策略。在这里,我们研究了与细菌性阴道病(BV)相关的厌氧细菌对HIV-1通过两种不同的树突状细胞(DC)亚群传播的影响,即炎症性单核细胞来源的DC (moDCs)和原发CD1c+ DC。值得注意的是,与其他bv相关的微生物群相比,timonensis Prevotella增强了modc和CD1c+ dc对HIV-1的摄取,并且增加的摄取不依赖于细胞HIV-1(共)受体。成像流式细胞术分析显示,HIV-1并不与血吸虫共定位,而是被内化到已知参与HIV-1传播的tetraspanin阳性区室中。P. timmonensis细菌通过CD1c+ dc增强HIV-1的传播,而不通过moDCs,并且增强的传播与病毒感染无关。我们的研究强烈表明,粘膜DC亚群在bv相关的HIV-1易感性中具有不同的功能,并强调了阴道生态失调的早期诊断和靶向治疗对于降低HIV-1获得风险的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Vaginal Prevotella timonensis Bacteria Enhance HIV-1 Uptake and Differentially Affect Transmission by Distinct Primary Dendritic Cell Subsets

Vaginal Prevotella timonensis Bacteria Enhance HIV-1 Uptake and Differentially Affect Transmission by Distinct Primary Dendritic Cell Subsets

Young females are at high risk of acquiring HIV-1 infections and an imbalance in the vaginal microbiome enhances susceptibility to HIV-1 infection. More insights into the underlying mechanisms could open up new strategies to prevent HIV-1 acquisition and dissemination. Here, we investigated the effect of anaerobic bacteria associated with bacterial vaginosis (BV) on HIV-1 transmission by two distinct dendritic cell (DC) subsets, that is, inflammatory monocyte-derived DCs (moDCs) and primary CD1c+ DCs. Notably, in contrast to other BV-associated microbiota, Prevotella timonensis enhanced uptake of HIV-1 by both moDCs and CD1c+ DCs and the increased uptake was independent of cellular HIV-1 (co-)receptors. Imaging flow cytometry analyses showed that HIV-1 did not co-localise with P. timonensis but was internalized into tetraspanin-positive compartments known to be involved in HIV-1 transmission. P. timonensis bacteria enhanced HIV-1 transmission by CD1c+ DCs, but not by moDCs, and the enhanced transmission was independent of viral infection. Our study strongly suggests that mucosal DC subsets have distinct functions in BV-associated HIV-1 susceptibility, and underscores the importance of early diagnosis and targeted treatment of vaginal dysbiosis to reduce the risk of HIV-1 acquisition.

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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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