Control of HIV infection by IFN-α: implications for latency and a cure

被引:0
|
作者
Nollaig M. Bourke
Silvia Napoletano
Ciaran Bannan
Suaad Ahmed
Colm Bergin
Áine McKnight
Nigel J. Stevenson
机构
[1] Trinity Translational Medicine Institute,School of Medicine
[2] Trinity College Dublin,Department of Medical Gerontology
[3] Mercer’s Institute for Successful Ageing,School of Biochemistry and Immunology
[4] St. James Hospital,Department of Genito Urinary Medicine and Infectious Diseases
[5] Trinity College Dublin,Blizard Institute School of Medicine and Dentistry
[6] St. James’s Hospital,undefined
[7] Queen Mary University of London,undefined
来源
关键词
HIV; Interferon; Latency; Anti-viral; JAK/STAT; Cure;
D O I
暂无
中图分类号
学科分类号
摘要
Viral infections, including HIV, trigger the production of type I interferons (IFNs), which in turn, activate a signalling cascade that ultimately culminates with the expression of anti-viral proteins. Mounting evidence suggests that type I IFNs, in particular IFN-α, play a pivotal role in limiting acute HIV infection. Highly active anti-retroviral treatment reduces viral load and increases life expectancy in HIV positive patients; however, it fails to fully eliminate latent HIV reservoirs. To revisit HIV as a curable disease, this article reviews a body of literature that highlights type I IFNs as mediators in the control of HIV infection, with particular focus on the anti-HIV restriction factors induced and/or activated by IFN-α. In addition, we discuss the relevance of type I IFN treatment in the context of HIV latency reversal, novel therapeutic intervention strategies and the potential for full HIV clearance.
引用
收藏
页码:775 / 783
页数:8
相关论文
共 50 条
  • [1] Control of HIV infection by IFN-α: implications for latency and a cure
    Bourke, Nollaig M.
    Napoletano, Silvia
    Bannan, Ciaran
    Ahmed, Suaad
    Bergin, Colm
    McKnight, Aine
    Stevenson, Nigel J.
    CELLULAR AND MOLECULAR LIFE SCIENCES, 2018, 75 (05) : 775 - 783
  • [2] IFN-ε protects primary macrophages against HIV infection
    Tasker, Carley
    Subbian, Selvakumar
    Gao, Pan
    Couret, Jennifer
    Levine, Carly
    Ghanny, Saleena
    Soteropoulos, Patricia
    Zhao, Xilin
    Landau, Nathaniel
    Lu, Wuyuan
    Chang, Theresa L.
    JCI INSIGHT, 2016, 1 (20)
  • [3] The predominant role of IFN-γ in the neuropathogenesis of HIV-1 infection
    Shapshak, P
    Duncan, R
    Minagar, A
    Goodkin, K
    NEUROLOGY, 2001, 56 (08) : A476 - A476
  • [4] IFN-λ Inhibits Drug-Resistant HIV Infection of Macrophages
    Wang, Xu
    Wang, He
    Liu, Man-Qing
    Li, Jie-Liang
    Zhou, Run-Hong
    Zhou, Yu
    Wang, Yi-Zhong
    Zhou, Wang
    Ho, Wen-Zhe
    FRONTIERS IN IMMUNOLOGY, 2017, 8
  • [5] Understanding HIV Latency: The Road to an HIV Cure
    Dahabieh, Matthew S.
    Battivelli, Emilie
    Verdin, Eric
    ANNUAL REVIEW OF MEDICINE, VOL 66, 2015, 66 : 407 - 421
  • [6] STAT1 regulates IFN-αβ- and IFN-γ-dependent control of infection with Chlamydia pneumoniae by nonhemopoietic cells
    Rothfuchs, Antonio Gigliotti
    Trumstedt, Christian
    Mattei, Fabrizio
    Schiavoni, Giovanna
    Hidmark, Asa
    Wigzell, Hans
    Rottenberg, Martin E.
    JOURNAL OF IMMUNOLOGY, 2006, 176 (11): : 6982 - 6990
  • [7] Associations of IFN-γ polymorphism with HIV-1 infection in the Korean population
    Kang, MW
    Pyo, CW
    Wie, SH
    Choi, HB
    Kim, Y
    Kim, YK
    Lee, JS
    Kim, TG
    AIDS RESEARCH AND HUMAN RETROVIRUSES, 2006, 22 (03) : 297 - 299
  • [8] Re-examining IFN-α treatment for HIV-1 infection
    McCarthy, Jacob
    FUTURE VIROLOGY, 2012, 7 (04) : 337 - 337
  • [9] Control of IFN-αA by CD73:: Implications for mucosal inflammation
    Louis, Nancy A.
    Robinson, Andreas M.
    MacManus, Christopher F.
    Karhausen, Joern
    Scully, Melanie
    Colgan, Sean P.
    JOURNAL OF IMMUNOLOGY, 2008, 180 (06): : 4246 - 4255
  • [10] Targeting IFN-: therapeutic implications
    Eslam, Mohammed
    George, Jacob
    EXPERT OPINION ON THERAPEUTIC TARGETS, 2016, 20 (12) : 1425 - 1432