咨询与建议

看过本文的还看了

相关文献

该作者的其他文献

文献详情 >The role of RIP3 in the induct... 收藏
The role of RIP3 in the induction of influenza viral antigen...

The role of RIP3 in the induction of influenza viral antigen specific CD8+T cell responses in C57BL/6 mice upon H1N1influenza virus infection

作     者:Boyin Qin Chao Wang Lixiang Chen Yang Liu Xiaonan Ren Bin Wu Shun Li Xiaohui Zhou 

作者单位:Shanghai public health clinical center 

会议名称:《第十四届全国免疫学学术大会》

会议日期:2021年

学科分类:1001[医学-基础医学(可授医学、理学学位)] 100102[医学-免疫学] 10[医学] 

关 键 词:Receptor-interacting protein 3(RIP3) H1N1 influenza virus antigen specific CD8+T cells 

摘      要:Objective:The purpose of this study was to explore whether RIP3 is involved in the induction and function of antigen-specific CD8T cells and memory CD8T cells in mice infected with influenza A virus ***:RIP3 and WT mice were infected through intranasal with influenza A H1 N1 PR8 virus(0.5 x LD50),*** spleen and peripheral blood of mice were dissected and collected in the post-infection effect stage(7 days after infection),memory formation stage β7 days after infection) and memory response stage β days after reinfection).The number and proportion of virus-specific effector CD8+T cells were detected by flow cytometry,and the expression of cytokines IFN-γ,TNF-α,IL-2 and GranzymeB were detected by flow *** the same time,the expression of immune checkpoint molecules PD-1,LAG-3,Tim-3 and CTLA-4 of CD8CD44 T cell subsets in mouse spleen was *** proportion of CD8T cells differentiated into TCM and TEM/TEff in the memory response phase was also ***:In the effect stage,there were few influenza antigen-specific CD8T cells in the spleen of RIP3 infected mice,and the expression levels of effector cytokines IFN-γ,TNF-α,IL-2 and GranzymeB on CD8+T cells were significantly lower than those in WT *** the same time,the immune checkpoint molecules LAG-3 and Tim-3 expressed by CD8+T cells in RIP3 infected group were significantly lower than those in WT *** the memory stage,the number of antigen-specific CD8T cells in peripheral blood of RIP3 mice was significantly lower than that of WT *** the stage of memory response,the number of antigen-specific CD8T cells produced by RIP3 mice and the ability of CD8T cells to secrete IFN-y were significantly lower than those of WT *** the phenotypes of activated memory CD8+T cells,the proportion of TEM in WT mice was significantly higher than that in RIP3 mice,while the proportion of TCM in WT mice was significantly lower than that in RIP3 ***:This study suggests t

读者评论 与其他读者分享你的观点

用户名:未登录
我的评分