Mechanisms of Endogenous HIV-1 Reactivation by Endocervical Epithelial Cells

Author:

Gornalusse Germán G.1ORCID,Valdez Rogelio2,Fenkart Gabriella2,Vojtech Lucia1ORCID,Fleming Lamar M.2,Pandey Urvashi1ORCID,Hughes Sean M.1ORCID,Levy Claire N.1ORCID,dela Cruz Erin J.23ORCID,Calienes Fernanda L.2ORCID,Kirby Anna C.1,Fialkow Michael F.1,Lentz Gretchen M.1,Wagoner Jessica4,Jing Lichen5,Koelle David M.25467ORCID,Polyak Stephen J.4ORCID,Fredricks David N.25ORCID,McElrath M. Juliana254ORCID,Wald Anna2568ORCID,Hladik Florian125ORCID

Affiliation:

1. Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington, USA

2. Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA

3. Medical Scientist Training Program, Molecular and Cellular Biology Graduate Program, University of Washington School of Medicine, Seattle, Washington, USA

4. Department of Laboratory Medicine, University of Washington, Seattle, Washington, USA

5. Department of Medicine, Division of Allergy and Infectious Diseases, University of Washington, Seattle, Washington, USA

6. Department of Global Health, University of Washington, Seattle, Washington, USA

7. Benaroya Research Institute, Seattle, Washington, USA

8. Department of Epidemiology, University of Washington, Seattle, Washington, USA

Abstract

A reason that there is no universal cure for HIV-1 is that the virus can hide in the genome of infected cells in the form of latent proviral DNA. This hidden provirus is protected from antiviral drugs until it eventually reactivates to produce new virions. It is not well understood where in the body or how this reactivation occurs. We studied HIV-1 reactivation in the female genital tract, which is often the portal of HIV-1 entry and which remains a site of infection throughout the disease. We found that the columnar epithelial cells lining the endocervix, the lower part of the uterus, are particularly effective in reactivating HIV-1 from infected T cells. This activity was enhanced by certain microbial stimuli, including herpes simplex virus 2, and blocked by antibodies against the inflammatory cytokine TNF-α. Avoiding HIV-1 reactivation could be important for maintaining a functional HIV-1 cure when antiviral therapy is stopped.

Funder

HHS | NIH | National Institute of Allergy and Infectious Diseases

HHS | NIH | National Institute on Drug Abuse

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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