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在意外感染HIV-1的实验室工作人员中鉴定针对同源病毒蛋白的型特异性细胞毒性T淋巴细胞反应。

Identification of type-specific cytotoxic T lymphocyte responses to homologous viral proteins in laboratory workers accidentally infected with HIV-1.

作者信息

Sipsas N V, Kalams S A, Trocha A, He S, Blattner W A, Walker B D, Johnson R P

机构信息

AIDS Research Center, Infectious Disease Unit, Massachusetts General Hospital, Charlestown 02129, USA.

出版信息

J Clin Invest. 1997 Feb 15;99(4):752-62. doi: 10.1172/JCI119221.

Abstract

Characterization of the cytotoxic T lymphocyte (CTL) response against HIV-1 has been limited by the use of target cells expressing viral proteins from laboratory isolates of HIV-1. This approach has favored identification of group-specific CTL responses and precluded assessment of the extent of type-specific CTL responses directed against HIV-1. Using cells expressing viral proteins from the HIV-1 IIIB strain, we performed a detailed characterization of HIV-1-specific CTL response in three laboratory workers accidentally infected with HIV-1 IIIB. Eight of the epitopes identified were group specific, lying in relatively conserved regions of Gag, reverse transcriptase, and envelope. Three type-specific epitopes were identified, two of them in highly variable regions of envelope. In longitudinal studies in one subject, seven different epitopes and five different restricting HLA class I alleles were identified, with a progressive increase in the number of CTL epitopes recognized by this subject over time. Our data demonstrate that type-specific CTL responses make up a significant proportion of the host cellular immune response against HIV-1 and that a broadening of epitope specificity may occur.

摘要

针对HIV-1的细胞毒性T淋巴细胞(CTL)反应的特征描述一直受到限制,这是因为使用了表达来自HIV-1实验室分离株的病毒蛋白的靶细胞。这种方法有利于识别群体特异性CTL反应,却排除了对针对HIV-1的型特异性CTL反应程度的评估。我们使用表达来自HIV-1 IIIB株病毒蛋白的细胞,对三名意外感染HIV-1 IIIB的实验室工作人员体内的HIV-1特异性CTL反应进行了详细的特征描述。所鉴定出的八个表位是群体特异性的,位于Gag、逆转录酶和包膜的相对保守区域。鉴定出了三个型特异性表位,其中两个位于包膜的高度可变区域。在对一名受试者的纵向研究中,鉴定出了七个不同的表位和五个不同的限制性HLA I类等位基因,随着时间的推移,该受试者识别的CTL表位数量逐渐增加。我们的数据表明,型特异性CTL反应在宿主针对HIV-1的细胞免疫反应中占很大比例,并且可能会出现表位特异性的拓宽。

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