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与1型人类免疫缺陷病毒反应的人细胞毒性T淋巴细胞克隆的长期培养及精细特异性

Long-term culture and fine specificity of human cytotoxic T-lymphocyte clones reactive with human immunodeficiency virus type 1.

作者信息

Walker B D, Flexner C, Birch-Limberger K, Fisher L, Paradis T J, Aldovini A, Young R, Moss B, Schooley R T

机构信息

Infectious Disease Unit, Massachusetts General Hospital, Boston.

出版信息

Proc Natl Acad Sci U S A. 1989 Dec;86(23):9514-8. doi: 10.1073/pnas.86.23.9514.

Abstract

The definition of human immunodeficiency virus type 1 (HIV-1) immunogenic epitopes is central to the rational design of AIDS vaccine strategies. In this study, we have generated seven HIV-1 reverse transcriptase-specific cytotoxic T-lymphocyte (CTL) clones from the peripheral blood of two seropositive subjects. Epitopes recognized by these CTL clones were identified by using target cells infected with recombinant HIV-1-vaccinia virus vectors expressing truncated reverse transcriptase proteins and further defined by using target cells incubated with overlapping 25-amino acid synthetic reverse transcriptase peptides. Five different CTL epitopes were identified, and in each case recognition was restricted by class I human leukocyte antigens (HLA). Clones maintained specific cytolytic function in continuous culture for up to 11 months, requiring only periodic restimulation with a CD3-specific monoclonal antibody. These results indicate that HIV-1-specific, major histocompatibility class I-restricted CTL recognize multiple epitopes of a single viral gene product in conjunction with different host HLA antigens. In addition, they demonstrate that human virus-specific CTL can be grown in long-term culture without the need for reexposure to viral antigen.

摘要

1型人类免疫缺陷病毒(HIV-1)免疫原性表位的定义是合理设计艾滋病疫苗策略的核心。在本研究中,我们从两名血清反应阳性受试者的外周血中获得了7个HIV-1逆转录酶特异性细胞毒性T淋巴细胞(CTL)克隆。通过使用感染了表达截短逆转录酶蛋白的重组HIV-1-痘苗病毒载体的靶细胞来鉴定这些CTL克隆识别的表位,并通过使用与重叠的25个氨基酸合成逆转录酶肽孵育的靶细胞进一步确定。鉴定出5种不同的CTL表位,并且在每种情况下,识别都受I类人类白细胞抗原(HLA)限制。克隆在连续培养中长达11个月保持特异性溶细胞功能,仅需要用CD3特异性单克隆抗体进行定期再刺激。这些结果表明,HIV-1特异性、主要组织相容性复合体I类限制的CTL与不同的宿主HLA抗原结合识别单个病毒基因产物的多个表位。此外,它们证明人类病毒特异性CTL可以在长期培养中生长,而无需再次暴露于病毒抗原。

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