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检测人类T淋巴细胞上HLA/肽四聚体与T细胞受体复合物的结合情况。

Testing for HLA/peptide tetramer-binding to the T cell receptor complex on human T lymphocytes.

作者信息

Weder Pauline, Schumacher Ton N M, Spits Hergen, Luiten Rosalie M

机构信息

Division of Immunology, The Netherlands Cancer Institute/Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.

Tytgat Institute for Liver and Instestinal Research, Academic Medical Center, University of Amsterdam, The Netherlands.

出版信息

Results Immunol. 2012 May 10;2:88-96. doi: 10.1016/j.rinim.2012.04.001. eCollection 2012.

Abstract

HLA/peptide tetramers are frequently used for ex vivo monitoring of disease- or vaccine-induced T cell immune responses and for T cell epitope identification. However, when low-levels HLA/peptide tetramer-positive T cell populations are encountered, it is difficult to ascertain whether this represents a true T cell receptor (TCR)-mediated interaction or background signal. To address this issue, we have developed a method for both HLA class I and class II tetramer assays to confirm tetramer-binding to the TCR/CD3 complex. Preincubation of T cells with anti-CD3 mAb SPV-T3b and subsequent crosslinking interferes with the binding of HLA/peptide tetramers to the TCR/CD3 complex and thereby indicates to what extent HLA/peptide tetramer binds through interaction with TCR/CD3 complex. SPV-T3b pretreatment results in a 2- to 10-fold decrease in tetramer-binding intensity to antigen-specific CD8+ or CD4+ T cells, whereas background reactivity of HLA/peptide tetramers containing HIV-derived peptide in HIV-negative donors remained unchanged. SPV-T3b pretreatment forms a valuable tool to verify tetramer-based detection of antigen-specific T cells during the monitoring of immune responses in clinical studies.

摘要

HLA/肽四聚体常用于体外监测疾病或疫苗诱导的T细胞免疫反应以及T细胞表位鉴定。然而,当遇到低水平HLA/肽四聚体阳性T细胞群体时,很难确定这是真正的T细胞受体(TCR)介导的相互作用还是背景信号。为了解决这个问题,我们开发了一种用于HLA I类和II类四聚体检测的方法,以确认四聚体与TCR/CD3复合物的结合。用抗CD3单克隆抗体SPV-T3b对T细胞进行预孵育并随后进行交联,会干扰HLA/肽四聚体与TCR/CD3复合物的结合,从而表明HLA/肽四聚体通过与TCR/CD3复合物相互作用结合的程度。SPV-T3b预处理导致与抗原特异性CD8+或CD4+ T细胞的四聚体结合强度降低2至10倍,而HIV阴性供体中含HIV衍生肽的HLA/肽四聚体的背景反应性保持不变。在临床研究免疫反应监测过程中,SPV-T3b预处理是验证基于四聚体检测抗原特异性T细胞的一种有价值的工具。

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