Update on the Impact of Depot Medroxyprogesterone Acetate on Vaginal Mucosal Endpoints and Relevance to Sexually Transmitted Infections.
Smritee DabeeChristina BalleMaricianah OnonoSteve InnesGonasagrie NairThesla Palanee-PhillipsAdam D BurgenerSteven E BosingerJo-Ann S PassmoreRenee HeffronHeather B JaspanAnna-Ursula HappelPublished in: Current HIV/AIDS reports (2023)
Although previous observational studies found women using DMPA-IM had higher abundance of bacterial vaginosis (BV)-associated bacteria, increased inflammation, increased cervicovaginal HIV target cell density, and epithelial barrier damage, sub-studies of the ECHO Trial found no adverse changes in vaginal microbiome, inflammation, proteome, transcriptome, and risk of viral and bacterial STIs, other than an increase in Th17-like cells. Randomised data suggest that DMPA-IM use does not adversely change mucosal endpoints associated with acquisition of infections. These findings support the safe use of DMPA-IM in women at high risk of acquiring STIs, including HIV.
Keyphrases
- antiretroviral therapy
- oxidative stress
- hiv positive
- hiv infected
- hiv testing
- polycystic ovary syndrome
- human immunodeficiency virus
- single cell
- clinical trial
- hepatitis c virus
- hiv aids
- men who have sex with men
- study protocol
- pregnancy outcomes
- rna seq
- open label
- magnetic resonance
- phase iii
- cervical cancer screening
- sars cov
- ulcerative colitis
- gene expression
- pregnant women
- double blind
- south africa
- computed tomography
- lipopolysaccharide induced
- skeletal muscle
- type diabetes
- phase ii
- cell therapy
- bone marrow
- diffusion weighted
- wastewater treatment
- data analysis
- dna methylation