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贝宁商业性工作者中HIV-1感染者全身和生殖道区室免疫调节细胞因子表达模式的差异。

Differences in immunoregulatory cytokine expression patterns in the systemic and genital tract compartments of HIV-1-infected commercial sex workers in Benin.

作者信息

Lajoie J, Poudrier J, Massinga-Loembe M, Guédou F, Agossa-Gbenafa C, Labbé A-C, Alary M, Roger M

机构信息

Laboratoire d'immunogénétique, Centre de Recherche du Centre Hospitalier de l'Université de Montréal, Canada.

出版信息

Mucosal Immunol. 2008 Jul;1(4):309-16. doi: 10.1038/mi.2008.18. Epub 2008 May 14.

Abstract

Initial exposure to human immunodeficiency virus type 1 (HIV-1) during heterosexual transmission occurs in the genital tract. Although much of the literature on the immune response to HIV-1 infection is based on studies performed at the systemic level, our understanding of tissue-specific immunity is lacking. Levels of both genital mucosal and blood interleukin (IL)-2, IL-4, IL-6, IL-10, tumor necrosis factor (TNF)-alpha, and interferon (IFN)-gamma production were compared between 57 HIV-1-uninfected and 52 HIV-1-infected female commercial sex workers (CSWs) as well as 73 HIV-1-uninfected non-CSW control women at low risk for exposure. HIV-1-infected CSWs had significantly higher genital mucosal levels of TNF-alpha and IFN-gamma compared with those in both the HIV-uninfected CSW and non-CSW groups. In contrast, the serum levels of all the cytokines tested were lower in HIV-1-infected CSWs compared with those in the other groups. The increased production of genital mucosal pro-inflammatory cytokines in HIV-1-infected CSWs possibly reflects susceptibility to HIV-1 infection and disease progression/perpetuation at the initial site of exposure.

摘要

在异性传播过程中,初次接触1型人类免疫缺陷病毒(HIV-1)发生在生殖道。尽管关于HIV-1感染免疫反应的许多文献是基于在全身水平进行的研究,但我们对组织特异性免疫仍缺乏了解。比较了57名未感染HIV-1的女性商业性工作者(CSW)、52名感染HIV-1的女性商业性工作者以及73名暴露风险低的未感染HIV-1的非CSW对照女性的生殖道黏膜和血液中白细胞介素(IL)-2、IL-4、IL-6、IL-10、肿瘤坏死因子(TNF)-α和干扰素(IFN)-γ的产生水平。与未感染HIV-1的CSW组和非CSW组相比,感染HIV-1的CSW的生殖道黏膜TNF-α和IFN-γ水平显著更高。相反,与其他组相比,感染HIV-1的CSW的所有检测细胞因子的血清水平更低。感染HIV-1的CSW生殖道黏膜促炎细胞因子产生增加可能反映了在初次接触部位对HIV-1感染以及疾病进展/持续存在的易感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14ba/3181215/f12f7f7c98f3/nihms719f1.jpg

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