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Use of Single Chain MHC Technology to Investigate Co-agonism in Human CD8+ T Cell Activation
Author(s) -
Xiang Zhao,
Maryam Hamidinia,
Joanna Ai Ling Choo,
Chien Tei Too,
Zi Zong Ho,
Ee Chee Ren,
Antonio Bertoletti,
Paul A. MacAry,
Keith G. Gould,
Joanna Brzostek,
Nicholas R. J. Gascoigne
Publication year - 2019
Publication title -
journal of visualized experiments
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.596
H-Index - 91
ISSN - 1940-087X
DOI - 10.3791/59126
Subject(s) - major histocompatibility complex , cd8 , t cell , mhc class i , microbiology and biotechnology , cytotoxic t cell , mhc restriction , biology , agonist , antigen , immune system , immunology , receptor , biochemistry , in vitro
Non-stimulatory self peptide MHC (pMHC) complexes do not induce T cell activation and effector functions, but can enhance T cell responses to agonist pMHC, through a process termed co-agonism. This protocol describes an experimental system to investigate co-agonism during human CD8+ T cell activation by expressing human MHC class I molecules presenting pre-determined peptides as single polypeptides (single chain MHC) in a xenogeneic cell line. We expressed single chain MHCs under conditions where low levels of agonist single chain p-MHC complexes and high levels of non-stimulatory single chain p-MHC complexes were expressed. Use of this experimental system allowed us to compare CD8+ T cell responses to agonist pMHC in the presence or absence of non-stimulatory pMHC. The protocol describes cell line transfection with single chain MHC constructs, generation of stable cell lines, culture of hepatitis B virus-specific human CD8+ T cells and T cell activation experiments simultaneously quantifying cytokine production and degranulation. The presented methods can be used for research on different aspects of CD8+ T cell activation in human T cell systems with known peptide MHC specificity.

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