Effects of heat shock protein gp96 on human dendritic cell maturation and CTL expansion

被引:31
|
作者
Zhang, YX
Zan, YL
Shan, M
Liu, CM
Shi, M
Li, W
Zhang, ZX
Liu, N
Wang, FS
Zhong, WD
Liao, FL
Gao, GF [1 ]
Tien, P
机构
[1] Chinese Acad Sci, Inst Microbiol, Mol Virol Res Ctr, Beijing 100080, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100080, Peoples R China
[3] Beijing 302 Hosp, Beijing 100039, Peoples R China
[4] Beijing Red Cross Blood Ctr, Histocompatibil Lab, Beijing 100088, Peoples R China
[5] Gilead Sci Inc, Foster City, CA 94404 USA
关键词
hepatitis B virus; heat shock protein gp96; monocyte-derived dendritic cells; cytotoxic T lymphocyte; peptide; transgenic mice;
D O I
10.1016/j.bbrc.2006.03.171
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We reported previously that heat shock protein gp96 and its N-terminal fragment were able to Stimulate CTL expansion specific for a HBV peptide (SYVNTNMGL) in BALB/c mice. Here we characterized the adjuvant effects of gp96 on human HLA-A2 restricted T cells. Full-length gp96 isolated from healthy human liver and recombinant fragments both from prokaryotic cells and eukaryotic cells were analyzed for their ability to stimulate maturation of human dendritic cells. It was found that in vitro these proteins were capable of maturating human monocyte-derived dendritic cells (MDDC) isolated from healthy donors as well as from HBV-positive, hepatocellular carcinoma (HCC) patients. In HLA-A2.1/Kb transgenic mice, gp96 and the recombinant fragments were found to augment CTL response specific for the HBcAg(18-27) FLPSDFFPSV peptide of hepatitis B virus. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:581 / 587
页数:7
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