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Frequency and Absolute Number of FoxP3^+ Regulatory T Cells Correlate with Disease Progression of Chronic HIV-1 Infection 被引量:1
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作者 Jun-liang FU fu-biao kang +6 位作者 Yan-mei JIAO Shao-jun XING Bao-yun FU Chun-bao ZHOU Xi-cheng WANG Hao WU Fu-Sheng WANG 《Virologica Sinica》 SCIE CAS CSCD 2007年第6期501-508,共8页
CD4^+CD25^+ Regulatory T cells (Treg) have been found to down-regulate immune activation in HIV-1 infection. However, whether the depletion of Treg benefits to the disease status of HIV infection remains undefined... CD4^+CD25^+ Regulatory T cells (Treg) have been found to down-regulate immune activation in HIV-1 infection. However, whether the depletion of Treg benefits to the disease status of HIV infection remains undefined. To address this issue, we enumerated the Treg absolute counts and frequency in 75 antiviral-naive HIV-1-infected individuals in this study. It was found that HIV-infected patients displayed a significant decline in Treg absolute counts but a significant increase in Treg frequency. In addition, with disease progression indicated by CD4 T-cell absolute counts, circulating Treg frequency gradually increased; while Treg absolute counts were gradually decreased, suggesting that the alteration of Treg number closely correlated with disease progression in HIV infection Functional analysis further showed that Treg efficiently inhibit both CD4 and CD8 T cell proliferation in vitro. Thus, our findings indicates that Treg actively participate in pathogenesis of chronic HIV infection, influencing the disease progression. 展开更多
关键词 T-LYMPHOCYTES HIV Infections Tolerance/Suppression/Anergy Proliferation
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Tricistronic hepatitis C virus subgenomic replicon expressing double transgenes
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作者 Xin Cheng Xiang-Cui Gao +7 位作者 Jun-Ping Wang Xin-Ying Yang Yan Wang Bao-Sheng Li fu-biao kang Hai-Jun Li Yue-Min Nan Dian-Xing Sun 《World Journal of Gastroenterology》 SCIE CAS 2014年第48期18284-18295,共12页
AIM: To construct a tricistronic hepatitis C virus (HCV) replicon with double internal ribosome entry sites (IRESes) of only 22 nucleotides for each, substituting the encephalomyocarditis virus (EMCV) IRESes, which ar... AIM: To construct a tricistronic hepatitis C virus (HCV) replicon with double internal ribosome entry sites (IRESes) of only 22 nucleotides for each, substituting the encephalomyocarditis virus (EMCV) IRESes, which are most often used as the translation initiation element to form HCV replicons. 展开更多
关键词 HEPACIVIRUS REPLICON Internal ribosome entry site Tricistronic expression
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