Anti-HIV Factors: Targeting Each Step of HIV’s Replication Cycle

Author(s): Marta Colomer-Lluch, Lauren S. Gollahon, Ruth Serra-Moreno

Journal Name: Current HIV Research

Volume 14 , Issue 3 , 2016

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Graphical Abstract:


Background: Similar to other animal viruses, HIV-1 relies on the contributions of the cellular machinery to ensure efficient virus propagation. However, human cells have evolved refined mechanisms to block key steps of the virus life-cycle, thereby suppressing viral replication. These cellular proteins are generally known as restriction factors, and they provide an early antiviral defense. So far, five potent restriction factors have been shown to effectively block HIV and/or SIV replication. These are TRIM5 proteins, SAMHD-1, members of the APOBEC3 (A3) family, Mx2 and Tetherin/BST-2. Results: Here, we review the antiviral mechanisms of these and other antiviral factors, their interaction with the innate immune responses, and how their functions might be exploited to clear and prevent HIV infection. Conclusion: Since the majority of vaccine approaches against HIV have failed so far, it is imperative to start looking at alternative strategies for vaccine and therapy development. By better understanding how HIV hijacks the cellular machinery for its own benefit in completing its life-cycle, and how the virus adapts to circumvent our intrinsic immunity, we will be better equipped to design compounds that specifically interrupt virus replication and spread.

Keywords: Antiviral factors, TRIM5, SAMHD-1, APOBEC3G, Mx2, BST-2, Tetherin, and BCA2.

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Article Details

Year: 2016
Published on: 04 March, 2016
Page: [175 - 182]
Pages: 8
DOI: 10.2174/1570162X14999160224094621
Price: $65

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