T cell activation, apoptosis and cytokine dysregulation in the (co)pathogenesis of HIV and pulmonary tuberculosis (TB)

被引:63
作者
Hertoghe, T
Wajja, A
Ntambi, L
Okwera, A
Aziz, MA
Hirsch, C
Johnson, J
Toossi, Z
Mugerwa, R
Mugyenyi, P
Colebunders, R
Ellner, J
Vanham, G
机构
[1] Inst Trop Med, Dept Microbiol, B-2000 Antwerp, Belgium
[2] Free Univ Brussels, Dept Physiol & Pathol, Brussels, Belgium
[3] Uganda Case Western Reserve Univ Res Collaborat, TB Project Clin, Mulago Hosp, Kampala, Uganda
[4] Minist Hlth, German Leprosy Relief Assoc, Natl TB & Leprosy Program, Kampala, Uganda
[5] Case Western Reserve Univ, TB Res Unit, Cleveland, OH 44106 USA
[6] Joint Clin Res Ctr, Kampala, Uganda
[7] Inst Trop Med, Dept Clin Sci, B-2000 Antwerp, Belgium
关键词
HIV; tuberculosis; apoptosis; interferon-gamma; transforming growth factor-beta;
D O I
10.1046/j.1365-2249.2000.01385.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:350 / 357
页数:8
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