MHC class I assembly: out and about

The assembly of major histocompatibility complex (MHC) class I molecules with peptides is orchestrated by several assembly factors including the transporter associated with antigen processing (TAP) and tapasin, the endoplasmic reticulum (ER) oxido-reductases ERp57 and protein disulfide isomerase (PD...

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Published inImmunology today (Amsterdam. Regular ed.) Vol. 29; no. 9; pp. 436 - 443
Main Authors Raghavan, Malini, Del Cid, Natasha, Rizvi, Syed Monem, Peters, Larry Robert
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.09.2008
Elsevier Limited
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Summary:The assembly of major histocompatibility complex (MHC) class I molecules with peptides is orchestrated by several assembly factors including the transporter associated with antigen processing (TAP) and tapasin, the endoplasmic reticulum (ER) oxido-reductases ERp57 and protein disulfide isomerase (PDI), the lectin chaperones calnexin and calreticulin, and the ER aminopeptidase (ERAAP). Typically, MHC class I molecules present endogenous antigens to cytotoxic T lymphocytes (CTLs). However, the initiation of CD8+ T-cell responses against many pathogens and tumors also requires the presentation of exogenous antigens by MHC class I molecules. We discuss recent developments relating to interactions and mechanisms of function of the various assembly factors and pathways by which exogenous antigens access MHC class I molecules.
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ISSN:1471-4906
0167-5699
1471-4981
DOI:10.1016/j.it.2008.06.004