Nondaily Preexposure Prophylaxis for HIV Prevention
PURPOSE OF REVIEW:
To
discuss nondaily preexposure prophylaxis (PrEP) modalities that may provide
advantages compared with daily PrEP in cost and cumulative toxicity, but may
have lower adherence forgiveness.
RECENT FINDINGS:
Animal
models have informed our understanding of early viral transmission events,
which help guide event-driven PrEP dosing strategies. These models indicate
early establishment of viral replication in rectal or cervicovaginal tissues,
so event-driven PrEP should rapidly deliver high mucosal drug concentrations
within hours of the potential exposure event. Macaque models have demonstrated
the high biological efficacy for event-driven dosing of oral tenofovir
disoproxil fumarate (TDF) and emtricitabine (FTC) against both vaginal and
rectal virus transmission. In humans, the IPERGAY study demonstrated 86%
efficacy for event-driven oral TDF/FTC dosing among men who have sex with men
(MSM), while no similar efficacy data are available on women or heterosexual
men. The HPTN 067 study showed that certain MSM populations adhere well to
nondaily PrEP, whereas other populations of women adhere more poorly to nondaily
versus daily regimens. Pharmacokinetic studies following oral TDF/FTC dosing in
humans indicate that TFV-diphosphate (the active form of TFV) accumulates to
higher concentrations in rectal versus cervicovaginal tissue, but nonadherence
in trials complicates the interpretation of differential mucosal drug
concentrations.
SUMMARY:
Event-driven
dosing for TFV-based PrEP has promise for HIV prevention in MSM. Future
research of event-driven PrEP in women and heterosexual men should be guided by
a better understanding of the importance of mucosal drug concentrations for
PrEP efficacy and its sensitivity to adherence.
- 1Department of Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, Colorado bLaboratory Branch, Division of HIV/AIDS Prevention, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
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