细胞毒性T细胞
抗原
肽
主要组织相容性复合体
生物
链霉菌
细胞毒性
人口
四聚体
T淋巴细胞
病毒学
免疫系统
体外
免疫学
化学
抗原提呈细胞
分子生物学
生物化学
医学
酶
环境卫生
作者
John D. Altman,Paul Moss,Philip Goulder,Dan H. Barouch,Michael G. McHeyzer‐Williams,John I. Bell,Andrew J. McMichael,Mark M. Davis
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1996-10-04
卷期号:274 (5284): 94-96
被引量:3623
标识
DOI:10.1126/science.274.5284.94
摘要
Identification and characterization of antigen-specific T lymphocytes during the course of an immune response is tedious and indirect. To address this problem, the peptide-major histocompatability complex (MHC) ligand for a given population of T cells was multimerized to make soluble peptide-MHC tetramers. Tetramers of human lymphocyte antigen A2 that were complexed with two different human immunodeficiency virus (HIV)-derived peptides or with a peptide derived from influenza A matrix protein bound to peptide-specific cytotoxic T cells in vitro and to T cells from the blood of HIV-infected individuals. In general, tetramer binding correlated well with cytotoxicity assays. This approach should be useful in the analysis of T cells specific for infectious agents, tumors, and autoantigens.
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