Lubaki N M, Ray S C, Dhruva B, Quinn T C, Siliciano R F, Bollinger R C
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
J Infect Dis. 1997 Jun;175(6):1360-7. doi: 10.1086/516468.
A total of 82 human immunodeficiency virus (HIV)-1-specific cytolytic T lymphocyte (CTL) clones were isolated and characterized from 5 HIV-infected subjects, utilizing multiple HLA class I alleles. B62-restricted, HIV-1 gag-specific CTL clones isolated from a single blood sample from 1 subject used four different Vbeta gene rearrangements. Multiple CTL clones could be isolated from the same time point directed against HIV-1 gag, nef, and env from 1 subject. A prospective analysis resulted in the isolation of CTL clones from 1 subject directed against multiple HIV-1 antigens, including the same highly conserved nef peptide, over a 1-year period, in the absence of detectable circulating viral plasma RNA. These data suggest that in some persons without clinical progression and low levels of circulating HIV-1, the CTL response is polyclonal, is directed against multiple HIV-1 proteins, including highly conserved peptides within these proteins, and is maintained over time.
利用多种HLA I类等位基因,从5名HIV感染受试者中分离并鉴定了总共82个针对人类免疫缺陷病毒1型(HIV-1)的细胞毒性T淋巴细胞(CTL)克隆。从1名受试者的单个血样中分离出的受B62限制的、HIV-1 gag特异性CTL克隆使用了四种不同的Vβ基因重排。从1名受试者的同一时间点可以分离出多个针对HIV-1 gag、nef和env的CTL克隆。一项前瞻性分析导致在1名受试者中,在未检测到循环血浆病毒RNA的情况下,经过1年的时间分离出针对多种HIV-1抗原(包括相同的高度保守的nef肽)的CTL克隆。这些数据表明,在一些没有临床进展且循环HIV-1水平较低的人中,CTL反应是多克隆的,针对多种HIV-1蛋白,包括这些蛋白内的高度保守肽,并且随时间维持。