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
Cellular and Molecular Life Sciences | 2018年 / 75卷
关键词
HIV; Interferon; Latency; Anti-viral; JAK/STAT; Cure;
D O I
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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.
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页码:775 / 783
页数:8
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