Department of Obstetrics and Gynecology, University of Washington, Seattle, United States; Department of Medicine, University of Washington, Seattle, United States; Vaccine and Infectious Diseases Division, Fred Hutchinson Cancer Research Center, Seattle, United States
Adam Burgener
Department of Medical Microbiology, University of Manitoba, Winnipeg, Canada; National HIV and Retrovirology Laboratories, Public Health Agency of Canada, Winnipeg, Canada
Lamar Ballweber
Vaccine and Infectious Diseases Division, Fred Hutchinson Cancer Research Center, Seattle, United States
Raphael Gottardo
Vaccine and Infectious Diseases Division, Fred Hutchinson Cancer Research Center, Seattle, United States; Department of Biostatistics, University of Washington, Seattle, United States; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, United States
Lucia Vojtech
Department of Obstetrics and Gynecology, University of Washington, Seattle, United States
Slim Fourati
Vaccine and Gene Therapy Institute of Florida, Port Saint Lucie, United States
James Y Dai
Department of Biostatistics, University of Washington, Seattle, United States; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, United States
Mark J Cameron
Vaccine and Gene Therapy Institute of Florida, Port Saint Lucie, United States
Johanna Strobl
Vaccine and Infectious Diseases Division, Fred Hutchinson Cancer Research Center, Seattle, United States
Sean M Hughes
Department of Obstetrics and Gynecology, University of Washington, Seattle, United States
Craig Hoesley
Department of Medicine, University of Alabama, Birmingham, United States
Philip Andrew
FHI 360, Durham, United States
Sherri Johnson
FHI 360, Durham, United States
Jeanna Piper
Division of AIDS, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, United States
David R Friend
CONRAD, Eastern Virginia Medical School, Arlington, United States
T Blake Ball
Department of Medical Microbiology, University of Manitoba, Winnipeg, Canada; National HIV and Retrovirology Laboratories, Public Health Agency of Canada, Winnipeg, Canada
Ross D Cranston
University of Pittsburgh School of Medicine, Pittsburgh, United States; Microbicide Trials Network, Magee-Women's Research Institute, Pittsburgh, United States
Kenneth H Mayer
Fenway Health, Beth Israel Deaconess Hospital, Harvard Medical School, Boston, United States
M Juliana McElrath
Department of Medicine, University of Washington, Seattle, United States; Vaccine and Infectious Diseases Division, Fred Hutchinson Cancer Research Center, Seattle, United States; Department of Global Health, University of Washington, Seattle, United States
Ian McGowan
University of Pittsburgh School of Medicine, Pittsburgh, United States; Microbicide Trials Network, Magee-Women's Research Institute, Pittsburgh, United States
Tenofovir gel is being evaluated for vaginal and rectal pre-exposure prophylaxis against HIV transmission. Because this is a new prevention strategy, we broadly assessed its effects on the mucosa. In MTN-007, a phase-1, randomized, double-blinded rectal microbicide trial, we used systems genomics/proteomics to determine the effect of tenofovir 1% gel, nonoxynol-9 2% gel, placebo gel or no treatment on rectal biopsies (15 subjects/arm). We also treated primary vaginal epithelial cells from four healthy women with tenofovir in vitro. After seven days of administration, tenofovir 1% gel had broad-ranging effects on the rectal mucosa, which were more pronounced than, but different from, those of the detergent nonoxynol-9. Tenofovir suppressed anti-inflammatory mediators, increased T cell densities, caused mitochondrial dysfunction, altered regulatory pathways of cell differentiation and survival, and stimulated epithelial cell proliferation. The breadth of mucosal changes induced by tenofovir indicates that its safety over longer-term topical use should be carefully monitored. Clinical trial registration: NCT01232803.