Small molecule modulators of MHC class II antigen presentation: Mechanistic insights and implications for therapeutic application

被引:17
作者
Call, Melissa J. [1 ]
机构
[1] Univ Melbourne, Walter & Eliza Hall Inst Med Res, Struct Biol Div, Parkville, Vic 3052, Australia
关键词
MHC class II; HLA-DM; Small molecules; Antigen presentation; Peptides; HLA-DR MOLECULES; COMPLEX CLASS-II; PEPTIDE-RECEPTIVE STATE; CHAIN-DERIVED PEPTIDE; HELPER T-CELLS; INVARIANT CHAIN; COMPOUNDS ENHANCE; LIGAND-EXCHANGE; HYDROGEN-BONDS; IN-VIVO;
D O I
10.1016/j.molimm.2011.05.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Antigen presenting cells express MHC class II molecules bound to peptide fragments and are responsible for activating CD4(+) T cells that then broadly influence many branches of the immune response. A growing interest in developing strategies to therapeutically influence the peptides to which naive CD4(+). T cells are exposed has led to the hunt for small molecules that modulate peptide presentation through the MHC class 11 pathway. Over the past decade a number of small molecules have been discovered that show surprising diversity in both structure and putative mechanisms. This review discusses how these small molecules were identified and compares the mechanisms by which they may act with what is known about the endogenous peptide exchanger, HLA-DM. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1735 / 1743
页数:9
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