Brenchley J M, Knox K S, Asher A I, Price D A, Kohli L M, Gostick E, Hill B J, Hage C A, Brahmi Z, Khoruts A, Twigg H L, Schacker T W, Douek D C
Human Immunology Section, Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Mucosal Immunol. 2008 Jan;1(1):49-58. doi: 10.1038/mi.2007.5.
The mechanisms underlying the massive gastrointestinal tract CD4 T-cell depletion in human immunodeficiency virus (HIV) infection are not well understood nor is it clear whether similar depletion is manifest at other mucosal surfaces. Studies of T-cell and virus dynamics in different anatomical sites have begun to illuminate the pathogenesis of HIV-associated disease. Here, we studied depletion and HIV infection frequencies of CD4 T cells from the gastrointestinal tract, bronchoalveolar lavage (BAL), and blood with the frequencies and functional profiles of HIV-specific T cells in these anatomically distinct sites in HIV-infected individuals. The major findings to emerge were as follows: (i) depletion of gastrointestinal CD4 T cells is associated with high frequencies of infected CD4 T cells; (ii) HIV-specific T cells are present at low frequencies in the gastrointestinal tract compared to blood; (iii) BAL CD4 T cells are not massively depleted during the chronic phase; (iv) infection frequencies of BAL CD4 T cells are similar to those in blood; (v) significantly higher frequencies and increased functionality of HIV-specific T cells were observed in BAL compared to blood. Taken together, these data suggest mechanisms for mucosal CD4 T-cell depletion and interventions that might circumvent global depletion of mucosal CD4 T cells.
人类免疫缺陷病毒(HIV)感染导致胃肠道大量CD4 T细胞耗竭的机制尚未完全明确,而且其他黏膜表面是否也存在类似的耗竭情况也不清楚。对不同解剖部位T细胞和病毒动态的研究已开始阐明HIV相关疾病的发病机制。在此,我们研究了HIV感染者胃肠道、支气管肺泡灌洗(BAL)液和血液中CD4 T细胞的耗竭情况及HIV感染频率,并分析了这些解剖学上不同部位的HIV特异性T细胞的频率和功能特征。主要研究结果如下:(i)胃肠道CD4 T细胞的耗竭与被感染CD4 T细胞的高频率相关;(ii)与血液相比,胃肠道中HIV特异性T细胞的频率较低;(iii)在慢性期,BAL中的CD4 T细胞不会大量耗竭;(iv)BAL中CD4 T细胞的感染频率与血液中的相似;(v)与血液相比,BAL中HIV特异性T细胞的频率显著更高且功能增强。综合来看,这些数据提示了黏膜CD4 T细胞耗竭的机制以及可能规避黏膜CD4 T细胞整体耗竭的干预措施。