Curiel T J, Wong J T, Gorczyca P F, Schooley R T, Walker B D
Department of Medicine, University of Colorado Health Sciences Center, Denver 80262.
AIDS Res Hum Retroviruses. 1993 Jan;9(1):61-8. doi: 10.1089/aid.1993.9.61.
Virus-specific cytotoxic T lymphocytes (CTL) are frequently of the CD8+ surface phenotype, although CTL of the CD4+ surface phenotype have also been described. Published reports of CTL derived from peripheral blood mononuclear cells (PBMC) of individuals infected with human immunodeficiency virus type 1 (HIV-1) have described primarily cells of the CD8+ surface phenotype. However, CD4+ HIV-1 envelope-specific CTL have been reported after in vitro stimulation with HIV-1 envelope protein of peripheral blood cells obtained from HIV-1-seronegative donors, in peripheral blood cells after vaccination of HIV-1-seronegative persons with HIV-1 envelope proteins, and in cerebrospinal fluid cells of HIV-1-infected individuals. Recently, CD4+ HIV-1 gag-specific CTL were also reported. We now report a patient from whom we derived HIV-1 envelope-specific CTL cell lines of the CD4+ surface phenotype. Our cell culture technique did not employ exogenous viral antigenic stimulation, and may therefore yield cells that more closely reflect those in the underlying populations from which they were derived. These CTL did not appear to have the clear human leukocyte antigen (HLA) class II restriction pattern typically seen in CD4-expressing cells and were not functionally inhibited by anti-CD3 antibody. Further work will be required to define the role of CD4+ CTL in the pathogenesis of HIV-1 disease.
病毒特异性细胞毒性T淋巴细胞(CTL)通常具有CD8 +表面表型,不过也有关于CD4 +表面表型CTL的描述。来自感染1型人类免疫缺陷病毒(HIV-1)个体外周血单核细胞(PBMC)的CTL的已发表报告主要描述了CD8 +表面表型的细胞。然而,在使用从HIV-1血清阴性供体获得的外周血细胞的HIV-1包膜蛋白进行体外刺激后、HIV-1血清阴性者用HIV-1包膜蛋白接种后的外周血细胞中以及HIV-1感染个体的脑脊液细胞中,均已报告有CD4 + HIV-1包膜特异性CTL。最近,也有关于CD4 + HIV-1 gag特异性CTL的报告。我们现在报告一名患者,我们从其体内获得了具有CD4 +表面表型的HIV-1包膜特异性CTL细胞系。我们的细胞培养技术未采用外源性病毒抗原刺激,因此可能产生更能反映其来源的基础群体中细胞情况的细胞。这些CTL似乎没有在表达CD4的细胞中通常所见的明确的人类白细胞抗原(HLA)II类限制模式,并且不受抗CD3抗体的功能抑制。需要进一步开展工作来确定CD4 + CTL在HIV-1疾病发病机制中的作用。