Hertoghe T, Wajja A, Ntambi L, Okwera A, Aziz M A, Hirsch C, Johnson J, Toossi Z, Mugerwa R, Mugyenyi P, Colebunders R, Ellner J, Vanham G
Institute of Tropical Medicine, Department of Microbiology, Antwerp and Department of Physiology and Pathology, Free University of Brussels (VUB), Brussels, Belgium.
Clin Exp Immunol. 2000 Dec;122(3):350-7. doi: 10.1046/j.1365-2249.2000.01385.x.
Immune parameters were compared in four groups of Ugandan subjects: HIV-and HIV+ adult patients with active pulmonary TB (HIV- PTB n = 38; HIV+ PTB n = 28), patients with HIV infection only (n = 26) and PPD+ healthy controls (n = 25). Compared with healthy controls, CD4 and CD8 T cells from patients with HIV and/or PTB expressed more activation markers (HLA-DR, CD38); their CD8 T cells expressed more CD95 (pre-apoptosis) and less CD28 (co-stimulatory receptor). Peripheral blood mononuclear cells (PBMC) of patients with either HIV or PTB were impaired in interferon-gamma (IFN-gamma) production upon antigenic stimulation. PTB (with or without HIV) was characterized by monocytosis, granulocytosis, increased transforming growth factor-beta 1 production and PPD-induced apoptosis. In vivo CD4 T cell depletion, in vitro increased spontaneous CD4 T cell apoptosis and defects in IFN-gamma responses upon mitogenic stimulation were restricted to HIV+ subjects (with or without PTB). Overlapping and distinctive immune alterations, associated with PTB and HIV, might explain mutual unfavourable influences of both diseases.
未感染艾滋病毒和感染艾滋病毒的活动性肺结核成年患者(未感染艾滋病毒的肺结核患者n = 38;感染艾滋病毒的肺结核患者n = 28)、仅感染艾滋病毒的患者(n = 26)和结核菌素试验阳性的健康对照者(n = 25)。与健康对照者相比,感染艾滋病毒和/或肺结核患者的CD4和CD8 T细胞表达了更多的活化标志物(HLA-DR、CD38);他们的CD8 T细胞表达了更多的CD95(凋亡前期)且CD28(共刺激受体)表达较少。感染艾滋病毒或肺结核患者的外周血单个核细胞(PBMC)在抗原刺激后产生干扰素-γ(IFN-γ)的能力受损。肺结核(无论是否合并艾滋病毒感染)的特征为单核细胞增多、粒细胞增多、转化生长因子-β1产生增加以及结核菌素诱导的细胞凋亡。体内CD4 T细胞耗竭、体外有丝分裂原刺激后自发CD4 T细胞凋亡增加以及IFN-γ反应缺陷仅限于感染艾滋病毒的受试者(无论是否患有肺结核)。与肺结核和艾滋病毒相关的重叠且独特的免疫改变可能解释了这两种疾病相互不利的影响。