Cutting edge: Class I presentation of host peptides following HIV infection

被引:59
作者
Hickman, HD
Luis, AD
Bardet, W
Buchli, R
Battson, CL
Shearer, MH
Jackson, KW
Kennedy, RC
Hildebrand, WH
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Immunol & Microbiol, Oklahoma City, OK 73104 USA
[2] Univ Oklahoma, Hlth Sci Ctr, William K Warren Med Res Inst, Oklahoma City, OK 73104 USA
关键词
D O I
10.4049/jimmunol.171.1.22
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Class I MHC molecules bind intracellular peptides for presentation to cytotoxic T lymphocytes. Identification of peptides presented by class I molecules during infection is therefore a priority for detecting and targeting intracellular pathogens. To understand which host-encoded peptides distinguish HIV-infected cells, we have developed a mass spectrometric approach to characterize HLA-B*0702 peptides unique to or up-regulated on infected T cells. In this study, we identify 15 host proteins that are differentially presented on infected human T cells. Peptides with increased expression on HIV-infected cells were derived from multiple categories of cellular proteins including RNA binding proteins and cell cycle regulatory proteins. Therefore, comprehensive analysis of the B*0702 peptide repertoire demonstrates that marked differences in host protein presentation occur after HIV infection.
引用
收藏
页码:22 / 26
页数:5
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