首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Deletion mutant of human cytomegalovirus lacking US2-US6 and US11 maintains MHC class I expression and antigen presentation by infected dendritic cells.
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Deletion mutant of human cytomegalovirus lacking US2-US6 and US11 maintains MHC class I expression and antigen presentation by infected dendritic cells.

机译:缺少US2-US6和US11的人类巨细胞病毒的缺失突变体通过感染的树突细胞维持MHC I类表达和抗原呈递。

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摘要

A HCMV mutant of endothelial- and DC-tropic strain TB40/E lacking the described MHC downregulating genes US2-6 and US11 (RVTB40/E(4)DeltaUS11) was generated. We analyzed the susceptibility of DC to RVTB40/E(4)DeltaUS11 and subsequently studied antigen presentation and T-cell stimulation. Wildtype TB40/E- and RVTB40/E(4)DeltaUS11 showed no significant difference in the efficiency of infection of DC. Whereas infection with TB40/E induced downregulation of MHC I, no significant MHC I downregulation was observed on RVTB40/E(4)DeltaUS11-infected DC, indicating that the US2-6, US11 region encodes for the major genes relevant for MHC I downregulation. However, both viruses induced downregulation of MHC II, as well as CD40, CD80, CD86 and CD83 to the same levels. Stimulation of IFN-gamma production by HCMV-specific CD8+ T-cells by infected autologous DC correlated with the modulation of MHC expression. While TB40/E-infected DC did not efficiently stimulate IFN-gamma production, RVTB40/E(4)DeltaUS11-infected DC efficiently stimulated CD8+ T-cells to produce IFN-gamma.
机译:生成缺乏所述的MHC下调基因US2-6和US11(RVTB40 / E(4)DeltaUS11)的内皮和DC嗜性菌株TB40 / E的HCMV突变体。我们分析了DC对RVTB40 / E(4)DeltaUS11的敏感性,随后研究了抗原呈递和T细胞刺激。野生型TB40 / E-和RVTB40 / E(4)DeltaUS11在感染DC的效率上没有显着差异。 TB40 / E感染可引起MHC I下调,而在RVTB40 / E(4)DeltaUS11感染的DC上未观察到明显的MHC I下调,表明US2-6,US11区域编码与MHC I下调相关的主要基因。 。但是,两种病毒均诱导MHC II以及CD40,CD80,CD86和CD83的下调至相同水平。感染的自体DC刺激HCMV特异性CD8 + T细胞产生IFN-γ与MHC表达的调节有关。虽然TB40 / E感染的DC不能有效地刺激IFN-γ的产生,但RVTB40 / E(4)DeltaUS11感染的DC可以有效地刺激CD8 + T细胞产生IFN-γ。

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