T细胞受体
细胞生物学
T细胞
CD3型
CD28
化学
免疫学
主要组织相容性复合体
生物
抗原
分子生物学
免疫系统
CD8型
作者
Joachim Hagel,Lucy C. Garner,Matthew Bilton,Hema Mehta,Tianqi Leng,Carl-Philipp Hackstein,Prabhjeet Phalora,Ali Amini,Hossain Delowar Akther,Nicholas M. Provine,Matthew Edmans,Christian B. Willberg,Paul Klenerman
出处
期刊:Methods in molecular biology
日期:2019-12-02
卷期号:: 97-124
被引量:15
标识
DOI:10.1007/978-1-0716-0207-2_7
摘要
Mucosal-associated invariant T (MAIT) cells are an abundant innate-like T cell subset in humans, enriched in mucosal tissues and the liver. MAIT cells express a semi-invariant T cell receptor (TCR) and recognize microbial-derived riboflavin metabolites presented on the MHC Class I-like molecule MR1. In addition to activation via the TCR, MAIT cells can also be activated in response to cytokines such as IL-12 and IL-18, in contrast to conventional T cells. Here we describe TCR-dependent and -independent methods for MAIT cell activation. The TCR-dependent approaches include stimulation with microbead- or plate-bound anti-CD3/anti-CD28 antibodies, and with 5-OP-RU or paraformaldehyde (PFA)-fixed E. coli in the presence of antigen-presenting cells (APCs). The latter method includes a combination of TCR- and cytokine-mediated stimulation. The TCR-independent methods include direct stimulation with the recombinant cytokines IL-12 and IL-18, and indirect stimulation with TLR-4/TLR-8 agonists or influenza A virus in the presence of APCs. Finally, we outline a protocol to analyze activated MAIT cells using flow cytometry.
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