Regulation of HLA class II expression prevents allogeneic T-cell responses

被引:6
作者
Jaimes, Y. [1 ]
Seltsam, A. [2 ]
Eiz-Vesper, B. [1 ]
Blasczyk, R. [1 ]
Figueiredo, C. [1 ]
机构
[1] Hannover Med Sch, Inst Transfus Med, D-30625 Hannover, Germany
[2] Inst Springe, Blood Serv NSTOB, Springe, Germany
来源
TISSUE ANTIGENS | 2011年 / 77卷 / 01期
关键词
allogeneic transplantation; human leukocyte antigen-DM; human leukocyte antigen-DR; RNA interference; tolerance; MHC CLASS-II; MEDIATING ALLOGRAFT-REJECTION; RNA INTERFERENCE; ANTIGEN PRESENTATION; CLINICAL-RELEVANCE; LENTIVIRAL VECTORS; HIV-INFECTION; GENE-THERAPY; IFN-GAMMA; PATHWAY;
D O I
10.1111/j.1399-0039.2010.01576.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The delivery of HLA-DR- or HLA-DM-specific short hairpin RNAs (shRNAs) in a monocytic cell line caused a decrease by up to 85% and 75% at the respective mRNA level. Allogeneic T-cells stimulated with HLA-DM-silenced monocytes decreased to 30% granzyme B mRNA and interferon gamma (IFN-gamma) production in comparison with T-cells stimulated with monocytes expressing a non-specific shRNA. By contrast, HLA-DR-silenced monocytes did not induce proliferation, up-regulation of granzyme B mRNA levels or high IFN-gamma secretion by allogeneic T-cells vs HLA-DR expressing cells. Direct targeting of HLA-DR expression prevented more efficiently an allogeneic T-cell response in comparison with the knockdown of the expression of HLA-DM molecules. Silencing the expression of HLA-DR molecules might contribute to the development of new allogeneic cell-based therapeutic approaches.
引用
收藏
页码:36 / 44
页数:9
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