Chen Z W, Yamamoto H, Watkins D I, Levinson G, Letvin N L
New England Regional Primate Research Center, Harvard Medical School, Southborough, Massachusetts 01772-9102.
J Virol. 1992 Jun;66(6):3913-7. doi: 10.1128/JVI.66.6.3913-3917.1992.
To explore the structural basis for AIDS virus recognition by CD8+ lymphocytes, we sought to determine whether there is a diverse or restricted usage of T-cell receptors (TCR) by simian immunodeficiency virus of macaques (SIVmac) Gag-specific cytotoxic T lymphocytes (CTL) in the rhesus monkey. Six Gag-specific CTL clones were independently generated from an SIVmac-infected rhesus monkey. All six CTL clones recognized a single SIVmac Gag peptide in association with a single major histocompatibility complex class I gene product, Mamu-A*01. TCR alpha-chain sequences from these six CTL clones employed four different V alpha families and five different J alpha gene segments. In contrast, five of the six CTL clones expressed V beta genes that were members of the same family, a human V beta 23 homolog. Furthermore, only one J beta gene was expressed by four of the six CTL clones. These results indicate that TCR of SIVmac Gag-specific CTL from a rhesus monkey can exhibit a restricted usage of V beta gene families and J beta genes.
为了探究CD8 +淋巴细胞识别艾滋病病毒的结构基础,我们试图确定恒河猴中猕猴免疫缺陷病毒(SIVmac)Gag特异性细胞毒性T淋巴细胞(CTL)对T细胞受体(TCR)的使用是多样的还是受限的。从一只感染SIVmac的恒河猴中独立产生了六个Gag特异性CTL克隆。所有六个CTL克隆都识别与单个主要组织相容性复合体I类基因产物Mamu-A*01相关的单个SIVmac Gag肽。这六个CTL克隆的TCRα链序列使用了四个不同的Vα家族和五个不同的Jα基因片段。相比之下,六个CTL克隆中的五个表达的Vβ基因是同一家族的成员,即人类Vβ23的同源物。此外,六个CTL克隆中的四个仅表达一个Jβ基因。这些结果表明,来自恒河猴的SIVmac Gag特异性CTL的TCR在Vβ基因家族和Jβ基因的使用上可能受到限制。