A novel gel for targeting vaginal inflammation to prevent HIV transmission
Adolescent girls and young women in sub-Saharan Africa are up to 3 times more likely to be infected with HIV than their male peers. Subclinical genital inflammation, caused by a non-optimal vaginal microbiome lacking beneficial Lactobacillus species, is a key mechanism driving this difference. We have discovered that optimal vaginal Lactobacillus spp. make a product that has direct anti-inflammatory effects on cervicovaginal epithelial cells that could help prevent HIV.
Objective
This study will formulate and perform preclinical studies of an anti-inflammatory microbiota metabolite for in vivo evaluation.
Approach
Formulated gels will be assessed for their physicochemical properties, ability to dampen inflammation in cervicovaginal epithelial cells in vitro, kill non-optimal vaginal bacteria, and their safety in a three-dimensional vaginal tissue model.
Community impact
A non-optimal vaginal microbiome increases the risk of a women acquiring HIV by >4-fold and transmitting HIV to their male partners. Developing a vaginal gel that dampens genital inflammation could be used by women to decrease HIV transmission.
Partners
Funding partners
- NHMRC
- ACH2
- Campbell Foundation
- MRFF
Collaborators
- Dr LIndi Masson
- Professor Catriona Bradshaw
- Professor Jacques Ravel
- Dr Simon Moulton
- Dr Simon Cook
- Dr Seyoum Ayenhunie
- Dr Lenka Vodstrcil
- Professor Deborah Bateson
- Dr Erica Plummer
Project contacts

Professor Gilda Tachedjian
Head, Life Sciences Discipline; Head, Retroviral Biology and Antivirals Laboratory
Project team

Dr Celine Deffrasnes
Senior Research Officer

Dr Paula Ellenberg
Laboratory Manager

Associate Professor Anna Hearps
Deputy Program Director, Disease Elimination; Head, Infection, Inflammation and Innate Immunity
