在潜伏性结核感染人群中,HIV合并感染与结核分枝杆菌特异性CD4 T细胞HLA-DR表达增加相关。

IF 2.8 3区 医学 Q3 IMMUNOLOGY
Jeremiah Khayumbi , Loren E. Sasser , Taryn A. McLaughlin , Joshua Ongalo , Joan Tonui , Samuel Gurrion Ouma , Angie Campbell , Felix Hayara Odhiambo , Neel R. Gandhi , Chelimo Kiprotich , Cheryl L. Day
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引用次数: 0

摘要

艾滋病毒感染与CD4 T细胞对结核分枝杆菌(Mtb)的反应失调和发展为结核病的风险增加有关。HIV患者的mtb特异性CD4 T细胞产生Th1细胞因子的能力降低,因此我们利用基于流式细胞术的方法以细胞因子独立的方式测量mtb特异性CD4 T细胞中CD40L的表达。我们评估了肯尼亚成年潜伏结核分枝杆菌感染的Mtb特异性CD4反应的频率和表型,发现大多数Mtb特异性CD4 T细胞在缺乏IFN-γ的情况下表达CD40L,无论HIV感染状态如何。与未感染艾滋病毒的人相比,艾滋病毒感染者的mmb特异性CD4 T细胞上HLA-DR的表达增加。这些数据表明,mtb特异性CD4 T细胞中HLA-DR的表达可能代表了在症状性结核病发展之前HIV感染者中分枝杆菌抗原刺激增加的早期生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
HIV co-infection is associated with increased HLA-DR expression by Mycobacterium tuberculosis-specific CD4 T cells in people with latent tuberculosis infection
Infection with HIV is associated with dysregulated CD4 T cell responses to Mycobacterium tuberculosis (Mtb) and increased risk of developing tuberculosis. Mtb-specific CD4 T cells in people with HIV have diminished Th1 cytokine production capacity, thus we utilized a flow cytometry-based assay to measure CD40L expression by Mtb-specific CD4 T cells in a cytokine-independent manner. We evaluated the frequency and phenotype of Mtb-specific CD4 responses in Kenyan adults with latent Mtb infection and found that the majority of Mtb-specific CD4 T cells expressed CD40L in the absence of IFN-γ, regardless of HIV infection status. Expression of HLA-DR was increased on Mtb-specific CD4 T cells in people with HIV, compared to people without HIV. These data suggest expression of HLA-DR by Mtb-specific CD4 T cells may represent an early biomarker of increased mycobacterial antigen stimulation in people with HIV prior to the development of symptomatic tuberculosis disease.
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来源期刊
Tuberculosis
Tuberculosis 医学-呼吸系统
CiteScore
4.60
自引率
3.10%
发文量
87
审稿时长
49 days
期刊介绍: Tuberculosis is a speciality journal focusing on basic experimental research on tuberculosis, notably on bacteriological, immunological and pathogenesis aspects of the disease. The journal publishes original research and reviews on the host response and immunology of tuberculosis and the molecular biology, genetics and physiology of the organism, however discourages submissions with a meta-analytical focus (for example, articles based on searches of published articles in public electronic databases, especially where there is lack of evidence of the personal involvement of authors in the generation of such material). We do not publish Clinical Case-Studies. Areas on which submissions are welcomed include: -Clinical TrialsDiagnostics- Antimicrobial resistance- Immunology- Leprosy- Microbiology, including microbial physiology- Molecular epidemiology- Non-tuberculous Mycobacteria- Pathogenesis- Pathology- Vaccine development. This Journal does not accept case-reports. The resurgence of interest in tuberculosis has accelerated the pace of relevant research and Tuberculosis has grown with it, as the only journal dedicated to experimental biomedical research in tuberculosis.
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