Geretti A M, Dings M E, van Els C A, van Baalen C A, Wijnholds F J, Borleffs J C, Osterhaus A D
Institute of Virology, Erasmus University Rotterdam, Netherlands.
J Infect Dis. 1996 Jul;174(1):34-45. doi: 10.1093/infdis/174.1.34.
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.
对9名人类免疫缺陷病毒1型(HIV-1)感染者外周血单个核细胞中的HIV-1 Gag特异性和EB病毒(EBV)特异性细胞毒性T淋巴细胞前体(CTLp)频率进行了纵向研究。通过抗原特异性刺激,在HIV-1感染的整个过程中,甚至在显性疾病发作后,均可在体外检测到HIV-1 Gag特异性CTLp。然而,在4名患者中,在EBV特异性CTLp维持存在的情况下,HIV-1 Gag特异性CTLp频率随时间下降。这种下降与CD4细胞数量减少(r = 0.38;P < 0.05)和CD8细胞数量减少(r = 0.75;P < 0.001)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介导的免疫可能在更长时间内不受HIV-1诱导的免疫功能障碍的影响。与这一观察结果一致,EBV感染的淋巴母细胞样B细胞系可在体外支持EBV特异性CTL的生长,且不依赖于CD4细胞和外源性细胞因子。