Abstract |
Since HIV was identified as the etiological agent of AIDS, there have been significant advances in antiretroviral therapy (ART) that has reduced morbidity/mortality. Still, the viral genome's high mutation rate, suboptimal ART regimens, incomplete adherence to therapy and poor control of the viral load generate variants resistant to multiple drugs. Licensing over 30 anti-HIV drugs worldwide, including integrase inhibitors, has marked a milestone since they are potent and well-tolerated drugs. In addition, they favor a faster recovery of CD4+ T cells. They also increase the diversity profile of the gut microbiota and reduce inflammatory markers. All of these highlight the importance of including them in different ART regimens.
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Authors | John D Loaiza, Mateo Chvatal-Medina, Juan C Hernandez, Maria T Rugeles |
Journal | Immunotherapy
(Immunotherapy)
Vol. 15
Issue 17
Pg. 1477-1495
(12 2023)
ISSN: 1750-7448 [Electronic] England |
PMID | 37822251
(Publication Type: Journal Article, Review, Research Support, Non-U.S. Gov't)
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Chemical References |
- Anti-HIV Agents
- Integrase Inhibitors
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Topics |
- Humans
- Anti-HIV Agents
(pharmacology, therapeutic use)
- Integrase Inhibitors
(therapeutic use)
- HIV Infections
(drug therapy)
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