Role of Hydrogen Sulfide Gas in Modulating HIV 1 Latency and Reactivation

dc.contributor.guideSingh, Amit
dc.creator.researcherPal, Virender Kumar
dc.date.accessioned2022-12-20T10:26:30Z
dc.date.available2022-12-20T10:26:30Z
dc.date.awarded2022
dc.date.completed2021
dc.description.abstractHuman Immunodeficiency Virus 1 (HIV-1) remains a global public health threat, claiming 690 thousand people s lives in 2020 and causing 1.5 million new infections. The advent of combinatorial antiretroviral therapy (ART) have curbed the spread of the HIV-1 epidemic by limiting new infections rate. However, ART is not a curative therapy, and HIV-1 persists in latent reservoirs mainly comprising long-lived memory CD4+ T cells. Notably, low ART treatment coverage and cases of poor therapy adherence lead to replenishment of latent reservoirs and the emergence of drug-resistant variants. Thus, to eradicate HIV-1, it is important to understand how the virus establishes latency, maintains stable cellular reservoirs, and promotes rebound upon interruption of antiretroviral therapy (ART). Cellular redox status has been observed as a key determinant modulating HIV-1 latency and reactivation. HIV-1 patients display the hallmark of oxidative stress with reduced levels of major cellular antioxidants, glutathione (GSH), and thioredoxin (Trx) systems. The current approach to target latent HIV-1 includes a shock and kill approach, which utilizes latency reversing agents (LRAs) to reactivate HIV-1 and kill infected cells by immune-based mechanisms [Chapter 1]. The LRAs belonging to histone deacetylase inhibitors class, when used in combination with GSH biosynthesis inhibitor, BSO, induce robust oxidative stress and heightened HIV-1 reactivation. In this direction, the use of antioxidant molecules, e.g., N-acetyl cysteine (NAC), has been shown to limit HIV-1 reactivation, but the molecular mechanism involved in NAC action remains understudied. Recently, NAC has been shown to exert its effect by inducing the biogenesis of a novel antioxidant gasotransmitter molecule, hydrogen sulfide (H2S). Previously considered as a toxic gas, but literature in the past two decades suggests the cytoprotective and antioxidant role of H2S in several patho-physiological conditions. In this study,...
dc.format.accompanyingmaterialNone
dc.format.dimensions30
dc.format.extentvii, 154
dc.identifier.urihttp://hdl.handle.net/10603/428856
dc.languageEnglish
dc.publisher.institutionMicrobiology and Cell Biology
dc.publisher.placeBangalore
dc.publisher.universityIndian Institute of Science Bangalore
dc.rightsuniversity
dc.source.universityUniversity
dc.subject.keywordGenetics and Heredity
dc.subject.keywordLife Sciences
dc.subject.keywordMolecular Biology and Genetics
dc.titleRole of Hydrogen Sulfide Gas in Modulating HIV 1 Latency and Reactivation
dc.title.alternativeRole of Hydrogen Sulfide Gas in Modulating HIV-1 Latency and Reactivation
dc.type.degreePh.D.

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