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使用γ干扰素酶联免疫斑点分析(IFN-γ ELISPOT)鉴定和验证T细胞表位

Identification and validation of T-cell epitopes using the IFN-gamma ELISPOT assay.

作者信息

Wulf Markus, Hoehn Petra, Trinder Peter

机构信息

Thymed GmbH, Mikroforum Ring 2, 55234 Wendelsheim, Germany.

出版信息

Methods Mol Biol. 2009;524:439-46. doi: 10.1007/978-1-59745-450-6_32.

Abstract

The quest for new and enhanced vaccines requires improved means for identification of relevant antigens and the epitopes present within these. While CD8+ T cells recognize antigenic peptides presented in the context of MHC Class I, and play a key role in cellular immunity, CD4+ helper T-cells recognize antigens in the context of MHC Class II and assist other immune cells in orchestration of the defined immune response. Being a functional assay, ELISPOT can be used to define both MHC Class I and II epitopes as well as to validate them. Providing the quality of the cells used in the assay is sufficiently good, ELISPOT provides a solid platform for both screening and validating T-cell epitopes. While some ELISPOT assays rely upon loading of dendritic cells with antigen followed by incubation of HLA matched or autologous PBMC or enriched T cells, the assay presented here uses PBMC from diseased or vaccinated individuals to simultaneously identify and validate T-cell epitopes.

摘要

寻求新型和增强型疫苗需要改进识别相关抗原及其内部表位的方法。虽然CD8 + T细胞识别在MHC I类分子背景下呈递的抗原肽,并在细胞免疫中起关键作用,但CD4 +辅助性T细胞在MHC II类分子背景下识别抗原,并协助其他免疫细胞协调确定的免疫反应。作为一种功能性检测方法,ELISPOT可用于定义MHC I类和II类表位并对其进行验证。只要检测中使用的细胞质量足够好,ELISPOT就能为筛选和验证T细胞表位提供一个坚实的平台。虽然一些ELISPOT检测依赖于用抗原负载树突状细胞,然后孵育HLA匹配或自体的外周血单核细胞(PBMC)或富集的T细胞,但本文介绍的检测方法使用患病或接种疫苗个体的PBMC来同时识别和验证T细胞表位。

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