Flórido Manuela, Pearl John E, Solache Alejandra, Borges Margarida, Haynes Laura, Cooper Andrea M, Appelberg Rui
Laboratory of Microbiology and Immunology of Infection, Institute for Molecular and Cell Biology, University of Porto, Rua do Campo Alegre 823, 4150-180 Porto, Portugal.
Infect Immun. 2005 Jun;73(6):3577-86. doi: 10.1128/IAI.73.6.3577-3586.2005.
Infection by virulent Mycobacterium avium caused progressive severe lymphopenia in C57BL/6 mice due to increased apoptosis rates. T-cell depletion did not occur in gamma interferon (IFN-gamma)-deficient mice which showed increased T-cell numbers and proliferation; in contrast, deficiency in nitric oxide synthase 2 did not prevent T-cell loss. Although T-cell loss was IFN-gamma dependent, expression of the IFN-gamma receptor on T cells was not required for depletion. Similarly, while T-cell loss was optimal if the T cells expressed IFN-gamma, CD8(+) T-cell depletion could occur in the absence of T-cell-derived IFN-gamma. Depletion did not require that the T cells be specific for mycobacterial antigen and was not affected by deficiencies in the tumor necrosis factor receptors p55 or p75, the Fas receptor (CD95), or the respiratory burst enzymes or by forced expression of bcl-2 in hematopoietic cells.
致病性鸟分枝杆菌感染可导致C57BL/6小鼠因凋亡率增加而出现进行性严重淋巴细胞减少。在γ干扰素(IFN-γ)缺陷小鼠中未发生T细胞耗竭,这些小鼠的T细胞数量增加且增殖;相反,一氧化氮合酶2缺陷并不能阻止T细胞丢失。虽然T细胞丢失依赖于IFN-γ,但T细胞耗竭并不需要T细胞上表达IFN-γ受体。同样,虽然如果T细胞表达IFN-γ,T细胞丢失最为明显,但在没有T细胞来源的IFN-γ时,CD8(+) T细胞也会发生耗竭。耗竭并不要求T细胞对分枝杆菌抗原具有特异性,也不受肿瘤坏死因子受体p55或p75、Fas受体(CD95)、呼吸爆发酶缺陷的影响,也不受造血细胞中bcl-2的强制表达的影响。