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结核病治疗后的结核特异性反应:合并感染HIV的影响

Tuberculosis specific responses following therapy for TB: Impact of HIV co-infection.

作者信息

Siddiqui S, Sarro Y, Diarra B, Diallo H, Guindo O, Dabitao D, Tall M, Hammond A, Kassambara H, Goita D, Dembele P, Traore B, Hengel R, Nason M, Warfield J, Washington J, Polis M, Diallo S, Dao S, Koita O, Lane H C, Catalfamo M, Tounkara A

机构信息

Collaborative Clinical Research Branch, National Institutes of Allergy and Infectious Diseases, National Institutes of Health, Rm 1167, Bldg. 6700B, Rockledge Drive, Bethesda, MD 20892, USA.

Collaborative Clinical Research Branch, National Institutes of Allergy and Infectious Diseases, National Institutes of Health, Rm 1167, Bldg. 6700B, Rockledge Drive, Bethesda, MD 20892, USA.

出版信息

Clin Immunol. 2015 Jul;159(1):1-12. doi: 10.1016/j.clim.2015.04.002. Epub 2015 Apr 15.

Abstract

Characterizing perturbations in the immune response to tuberculosis in HIV can develop insights into the pathogenesis of coinfection. HIV+ TB+ and TB monoinfected (TB+) subjects recruited from clinics in Bamako prior to initiation of TB treatment were evaluated at time-points following initiation of therapy. Flow cytometry assessed CD4+/CD8+ T cell subsets and activation markers CD38/HLA-DR. Antigen specific responses to TB proteins were assessed by intracellular cytokine detection and proliferation. HIV+ TB+ subjects had significantly higher markers of immune activation in the CD4+ and CD8+ T cells compared to TB+ subjects. HIV+ TB+ had lower numbers of TB-specific CD4+ T cells at baseline. Plasma IFNγ levels were similar between HIV+ TB+ and TB+ subjects. No differences were observed in in-vitro proliferative capacity to TB antigens between HIV+ TB+ and TB+ subjects. Subjects with HIV+ TB+ coinfection demonstrate in vivo expansion of TB-specific CD4+ T cells. Immunodeficiency associated with CD4+ T cell depletion may be less significant compared to immunosuppression associated with HIV viremia or untreated TB infection.

摘要

表征HIV感染中对结核病免疫反应的扰动有助于深入了解合并感染的发病机制。在巴马科诊所招募的、在开始抗结核治疗前的HIV+TB+和单纯结核感染(TB+)受试者在开始治疗后的不同时间点进行了评估。流式细胞术评估CD4+/CD8+T细胞亚群以及活化标志物CD38/HLA-DR。通过细胞内细胞因子检测和增殖来评估对结核蛋白的抗原特异性反应。与TB+受试者相比,HIV+TB+受试者的CD4+和CD8+T细胞中免疫活化标志物显著更高。HIV+TB+受试者在基线时结核特异性CD4+T细胞数量较少。HIV+TB+和TB+受试者之间的血浆IFNγ水平相似。HIV+TB+和TB+受试者之间对结核抗原的体外增殖能力未观察到差异。HIV+TB+合并感染的受试者表现出结核特异性CD4+T细胞在体内的扩增。与HIV病毒血症或未经治疗的结核感染相关的免疫抑制相比,与CD4+T细胞耗竭相关的免疫缺陷可能不太显著。

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