Latency Reversal and Clearance of Persistent HIV Infection.

Methods Mol Biol

UNC HIV Cure Center, Department of Medicine, and Microbiology and Immunology, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, NC, USA.

Published: March 2022

AI Article Synopsis

  • Efforts to prevent and treat HIV have made progress, with effective antiretroviral therapy (ART) allowing those infected to live long, healthy lives similar to uninfected individuals.
  • The challenge remains due to the dormant HIV virus that requires lifelong ART to prevent resurgence of the infection.
  • Research is ongoing into "latency reversal" and immunotherapy strategies to eliminate the virus, suggesting that advances in treatment and prevention could significantly reduce the impact of HIV on society.

Article Abstract

Efforts to prevent and treat human immunodeficiency virus type 1 (HIV) infection have begun to blunt the spread of HIV infection. Potent, safe, and well-tolerated antiretroviral therapy (ART) allows those infected with HIV to attain a life expectancy similar to that of HIV-uninfected individuals. But the persistence of the quiescent retroviral genome, enforced by the natural proliferative responses of the immune system itself, and a delicate balance of regulators viral expression, mandates lifelong ART suppression to prevent rebound viremia and the return of disease.The approach to HIV eradication that has been studied the most extensively envisions adding therapies to induce the expression of quiescent HIV-1 genomes following the control of viremia by ART, paired with immunotherapies to clear persistent infection. Paired testing of latency reversal and clearance strategies has begun, but the field is still in its infancy and additional obstacles to HIV eradication may emerge. However, there is reason for optimism that together with advances in ART delivery and HIV prevention strategies, efforts in HIV cure research will markedly diminish the effect of the HIV pandemic on society.

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http://dx.doi.org/10.1007/978-1-0716-1871-4_25DOI Listing

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