PROCESSING PATHWAYS FOR PRESENTATION OF CYTOSOLIC ANTIGEN TO MHC CLASS-II-RESTRICTED T-CELLS

被引:182
作者
MALNATI, MS
MARTI, M
LAVAUTE, T
JARAQUEMADA, D
BIDDISON, W
DEMARS, R
LONG, EO
机构
[1] NIAID,IMMUNOGENET LAB,12441 PARKLAWN DR,ROCKVILLE,MD 20852
[2] HOSP GERMANS TRIAS & PUJOL,IMMUNOL UNIT,E-08916 BADALONA,SPAIN
[3] NINCDS,NEUROIMMUNOL BRANCH,BETHESDA,MD 20892
[4] UNIV WISCONSIN,GENET LAB,MADISON,WI 53706
关键词
D O I
10.1038/357702a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
ANTIGENS presented to CD4+ T cells derive primarily from exogenous proteins that are processed into peptides capable of binding to class II major histocompatibility complex (MHC) molecules in an endocytic compartment 1-4. In contrast, antigens presented to CD8+ T cells derive mostly from proteins processed in the cytosol, and peptide loading onto class I MHC molecules in an early exocytic compartment is dependent on a transporter for antigen presentation encoded in the class II MHC region 5-11. Endogenous cytosolic antigen can also be presented by class II molecules 12,13. Here we show that, unlike class I-restricted recognition of antigen, HLA-DR1-restricted recognition of cytosolic antigen occurs in mutant cells without a transporter for antigen presentation. In contrast, DR1-restricted recognition of a short cytosolic peptide is dependent on such a transporter. Thus helper T-cell epitopes can be generated from cytosolic antigens by several mechanisms, one of which is distinct from the classical class I pathway.
引用
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页码:702 / 704
页数:3
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