4.2 Review

The microbiome and HIV persistence: implications for viral remission and cure

Journal

CURRENT OPINION IN HIV AND AIDS
Volume 13, Issue 1, Pages 61-68

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/COH.0000000000000434

Keywords

cure; gut microbiome; HIV persistence; HIV/AIDS; remission

Funding

  1. National Institutes of Health (NIH) [R01 HD080474]
  2. Johns Hopkins University Center for AIDS Research
  3. NIH [P30AI094189, T32-AI052071]
  4. NIAID
  5. NCI
  6. NICHD
  7. NHLBI
  8. NIDA
  9. NIMH
  10. NIA
  11. FIC
  12. NIGMS
  13. NIDDK
  14. OAR
  15. EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT [R01HD080474] Funding Source: NIH RePORTER
  16. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [T32AI052071, P30AI094189] Funding Source: NIH RePORTER

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Purpose of review This article discusses the interaction between HIV infection, the gut microbiome, inflammation and immune activation, and HIV reservoirs, along with interventions to target the microbiome and their implications for HIV remission and cure. Recent findings Most studies show that HIV-infected adults have a gut microbiome associated with decreased bacterial richness and diversity, and associated systemic inflammation and immune activation. A unique set of individuals, elite controllers, who spontaneously control HIV replication, have a similar microbiome to HIV-uninfected individuals. Conversely, exposure to maternal HIV in infants was shown to alter the gut microbiome, even in infants who escaped perinatal infection. Emerging research highlights the importance of the metabolomics and metaproteomics of the gut microbiome, which may have relevance for HIV remission and cure. Together, these studies illustrate the complexity of the relationship between HIV infection, the gut microbiome, and its systemic effects. Summary Understanding the association of HIV with the microbiome, metabolome, and metaproteome may lead to novel therapies to decrease inflammation and immune activation, and impact HIV reservoir size and vaccine responses. Further research in this area is important to inform HIV remission and cure treatments.

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