沙眼衣原体能增强非活化的 PBMC 对 HIV 的感染。

EC microbiology Pub Date : 2022-04-01 Epub Date: 2022-03-08
Alina Veretennikova, Theresa L Chang
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引用次数: 0

摘要

性接触是艾滋病毒最常见的传播途径,沙眼衣原体(CT)和淋病奈瑟菌(GC)等性传播感染(STI)的同时存在会增加感染艾滋病毒的风险。抗生素治疗可降低性传播感染的发病率,但不能降低艾滋病毒的发病率。CT 和 GC 可激活 Toll 样受体(TLRs)2 和 4,它们是微生物感染的传感器,对于启动免疫反应以控制感染至关重要。我们以前的研究表明,GC 可通过激活 TLR2 而不是 TLR4 来增强原代静息 CD4+ T 细胞对 HIV 的感染。在本研究中,我们测定了活CT和固定CT以及不同种类的乳酸菌(包括L. jensenii和L. reuteri)对新鲜分离的PBMC感染HIV的影响。我们发现,用新鲜或固定的 CT 对新鲜分离的 PBMCs 进行预处理,能促进新鲜分离的 CD4+ T 细胞感染 HIV,而乳酸菌则不能。结合之前的报告,我们得出结论:CT 和 GC 等 STI(而非乳酸杆菌等共生菌)增强了 HIV 感染,这可能是通过免疫激活实现的。重要的是,固定 CT 对 HIV 感染的增强作用可能解释了抗生素治疗未能降低 HIV 感染率的原因。在性传播感染的情况下,应考虑采取抑制性传播感染生长和性传播感染介导的粘膜免疫激活的综合策略来预防艾滋病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Chlamydia trachomatis Enhances HIV Infection of Non-Activated PBMCs.

Sexual contact is the most common route of HIV transmission, and the concurrent presence of sexually transmitted infections (STIs) such as Chlamydia trachomatis (CT) and Neisseria gonorrhoeae (gonococcus, GC) is known to increase the HIV risk. Antibiotic treatment decreases the incidence of STIs but not HIV. CT and GC activate Toll-like receptors (TLRs) 2 and 4, which act as sensors of microbial infection are critical for initiating immune responses to control infection. We have previously shown that GC enhances HIV infection of primary resting CD4+ T cells through activation of TLR2 but not TLR4. In this study, we determined the effect of live and fixed CT and different species of lactobacilli including L. jensenii and L. reuteri on HIV infection of freshly isolated PBMCs. We found that pretreatment of freshly isolated PBMCs with fresh or fixed CT, but not lactobacilli, promoted HIV infection of freshly isolated CD4+ T cells. Together with our previous reports, we concluded that STIs such as CT and GC but not commensal bacteria like lactobacilli enhanced HIV infection, possibly through immune activation. Importantly, the enhancement effect of fixed CT on HIV infection may explain the failure of antibiotic treatments to reduce the HIV incidence. Combined strategies to inhibit STI growth and STI-mediated mucosal immune activation should be considered for HIV prevention in the settings of STIs.

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