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首页> 外文期刊>The Journal of Infectious Diseases >Human immunodeficiency virus type 1 (HIV-1)--and Epstein-Barr virus--specific cytotoxic T lymphocyte precursors exhibit different kinetics in HIV-1--infected persons.
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Human immunodeficiency virus type 1 (HIV-1)--and Epstein-Barr virus--specific cytotoxic T lymphocyte precursors exhibit different kinetics in HIV-1--infected persons.

机译:人类1型免疫缺陷病毒(HIV-1)和爱泼斯坦-巴尔病毒特异性细胞毒性T淋巴细胞前体在感染HIV-1的人群中表现出不同的动力学。

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摘要

The frequencies of human immunodeficiency virus type 1 (HIV-1) Gag- and Epstein-Barr virus (EBV)-specific cytotoxic T lymphocyte precursors (CTLp) were studied longitudinally in peripheral blood mononuclear cells from 9 HIV-1-infected persons. By antigen-specific stimulation, HIV-1 Gag-specific CTLp were detected in vitro throughout the course of HIV-1 infection, even after the onset of overt disease. In 4 patients, however, HIV-1 Gag-specific CTLp frequencies declined over time in the presence of maintained EBV-specific CTLp. This decline was correlated with decreasing CD4 (r = .38; P < .05) and CD8 (r = .75; P < .001) cell numbers. The maintenance of EBV-specific CTLp in patients with low CD4 cell numbers indicated that EBV-specific CTL-mediated immunity may remain longer unaffected by HIV-1-induced immune dysfunction. Consistent with this observation, the growth of EBV-specific CTL could be supported in vitro by EBV-infected lymphoblastoid B cell lines, independent of both CD4 cells and exogenous cytokines.
机译:在9个HIV-1感染者的外周血单个核细胞中纵向研究了人类1型免疫缺陷病毒(HIV-1)Gag和爱泼斯坦-巴尔病毒(EBV)特异性细胞毒性T淋巴细胞前体(CTLp)的频率。通过抗原特异性刺激,即使在明显的疾病发作之后,在整个HIV-1感染过程中仍在体外检测到HIV-1 Gag特异性CTLp。但是,在4例患者中,在维持EBV特异性CTLp的情况下,HIV-1 Gag特异性CTLp频率随时间下降。这种下降与CD4(r = .38; P <.05)和CD8(r = .75; P <.001)细胞数目减少相关。 CD4细胞数量低的患者中EBV特异性CTLp的维持表明EBV特异性CTL介导的免疫力可能会保持更长的时间,不受HIV-1诱导的免疫功能障碍的影响。与该观察结果一致,EBV感染的淋巴母细胞B细胞系可在体外支持EBV特异性CTL的生长,而与CD4细胞和外源细胞因子无关。

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