Manipulating the Interferon Signaling Pathway: Implications for HIV Infection
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  • 英文篇名:Manipulating the Interferon Signaling Pathway: Implications for HIV Infection
  • 作者:Krystelle ; Nganou-Makamdop ; Daniel ; C.Douek
  • 英文作者:Krystelle Nganou-Makamdop;Daniel C.Douek;Institute of Clinical and Molecular Virology, University Hospital Erlangen;Human Immunology Section, Vaccine Research Center,National Institute of Allergy and Infectious Disease, National Institutes of Health;
  • 英文关键词:Human immunodeficiency virus(HIV);;Simian immunodeficiency virus(SIV);;Type I interferon(IFN-I);;Inflammation
  • 中文刊名:ZBDX
  • 英文刊名:中国病毒学(英文版)
  • 机构:Institute of Clinical and Molecular Virology, University Hospital Erlangen;Human Immunology Section, Vaccine Research Center,National Institute of Allergy and Infectious Disease, National Institutes of Health;
  • 出版日期:2019-04-15
  • 出版单位:Virologica Sinica
  • 年:2019
  • 期:v.34
  • 语种:英文;
  • 页:ZBDX201902007
  • 页数:5
  • CN:02
  • ISSN:42-1760/Q
  • 分类号:80-84
摘要
During human immunodeficiency virus(HIV) infection, type I interferon(IFN-I) signaling induces an antiviral state that includes the production of restriction factors that inhibit virus replication, thereby limiting the infection. As seen in other viral infections, type I IFN can also increase systemic immune activation which, in HIV disease, is one of the strongest predictors of disease progression to acquired immune deficiency syndrome(AIDS) and non-AIDS morbidity and mortality.Moreover, IFN-I is associated with CD4 T cell depletion and attenuation of antigen-specific T cell responses. Therefore,therapeutic manipulation of IFN-I signaling to improve HIV disease outcome is a source of much interest and debate in thefield. Recent studies have highlighted the importance of timing(acute vs. chronic infection) and have suggested that specific targeting of type I IFNs and their subtypes may help harness the beneficial roles of the IFN-I system while avoiding its deleterious activities.
        During human immunodeficiency virus(HIV) infection, type I interferon(IFN-I) signaling induces an antiviral state that includes the production of restriction factors that inhibit virus replication, thereby limiting the infection. As seen in other viral infections, type I IFN can also increase systemic immune activation which, in HIV disease, is one of the strongest predictors of disease progression to acquired immune deficiency syndrome(AIDS) and non-AIDS morbidity and mortality.Moreover, IFN-I is associated with CD4 T cell depletion and attenuation of antigen-specific T cell responses. Therefore,therapeutic manipulation of IFN-I signaling to improve HIV disease outcome is a source of much interest and debate in thefield. Recent studies have highlighted the importance of timing(acute vs. chronic infection) and have suggested that specific targeting of type I IFNs and their subtypes may help harness the beneficial roles of the IFN-I system while avoiding its deleterious activities.
引文
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