Defective antigen processing in GILT-free mice

被引:223
作者
Maric, M
Arunachalam, B
Phan, UT
Dong, C
Garrett, WS
Cannon, KS
Alfonso, C
Karlsson, L
Flavell, RA
Cresswell, P [1 ]
机构
[1] Yale Univ, Howard Hughes Med Inst, Immunol Sect, New Haven, CT 06520 USA
[2] RW Johnson Pharmaceut Res Inst, San Diego, CA 92121 USA
关键词
D O I
10.1126/science.1065500
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
Processing of proteins for major histocompatibility complex (MHC) class II-restricted presentation to CD4-positive T lymphocytes occurs after they are internalized by antigen-presenting cells (APCs). Antigenic proteins frequently contain disulfide bonds, and their reduction in the endocytic pathway facilitates processing. In humans, a gamma interferon-inducible lysosomal thiol reductase (GILT) is constitutively present in late endocytic compartments of APCs. Here, we identified the mouse homolog of GILT and generated a GILT knockout mouse. GILT facilitated the processing and presentation to antigen-specific T cells of protein antigens containing disulfide bonds. The response to hen egg lysozyme, a model antigen with a compact Structure containing four disulfide bonds, was examined in detail.
引用
收藏
页码:1361 / 1365
页数:5
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