Nanoformulations of Rilpivirine for Topical Pericoital and Systemic Coitus-Independent Administration Efficiently Prevent HIV Transmission
Open accessAbstract
Vaginal HIV transmission accounts for the majority of new infections worldwide. Currently, multiple efforts to prevent HIV transmission are based on pre-exposure prophylaxis with various antiretroviral drugs. Here, we describe two novel nanoformulations of the reverse transcriptase inhibitor rilpivirine for pericoital and coitus-independent HIV prevention. Topically applied rilpivirine, encapsulated in PLGA nanoparticles, was delivered in a thermosensitive gel, which becomes solid at body temperature. PLGA nanoparticles with encapsulated rilpivirine coated the reproductive tract and offered significant protection to BLT humanized mice from a vaginal high-dose HIV-1 challenge. A different nanosuspension of crystalline rilpivirine (RPV LA), administered intramuscularly, protected BLT mice from a single vaginal high-dose HIV-1 challenge one week after drug administration. Using transmitted/founder viruses, which were previously shown to establish de novo infection in humans, we demonstrated that RPV LA offers significant protection from two consecutive high-dose HIV-1 challenges one and four weeks after drug administration. In this experiment, we also showed that, in certain cases, even in the presence of drug, HIV infection could occur without overt or detectable systemic replication until levels of drug were reduced. We also showed that infection in the presence of drug can result in acquisition of multiple viruses after subsequent exposures. These observations have important implications for the implementation of long-acting antiretroviral formulations for HIV prevention. They provide first evidence that occult infections can occur, despite the presence of sustained levels of antiretroviral drugs. Together, our results demonstrate that topically- or systemically administered rilpivirine offers significant coitus-dependent or coitus-independent protection from HIV infection.
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An alternative approach tested in mice involves injecting a solution of the drug and polymer in an organic solvent subcutaneously, forming a surgically removable drug depot (~0.75 cm diameter in mice).
“An alternative approach was recently tested in mice and involves injecting a solution of the drug and polymer in an organic solvent subcutaneously 97 . A surgically removable drug depot (~0.75 cm diameter in mice) forms as the organic solvent diffuses out of the injection site.”
From Nanotechnology approaches for global infectious diseases (2021) · cites this paper as [97]
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References 49 · Cited by 77
- Authors
- Kovarova, M., Council, O. D., Date, A. A., Long, J. M., Nochii, T., Belshan, M., Shibata, A., Vincent, H., Baker, C. E., Thayer, W. O., Kraus, G., Lachaud-Durand, S., Williams, P., Destache, C. J., & Garcia, J. V.
- Affiliations
- University of North Carolina at Chapel Hill (US)
- Creighton University (US)
- Janssen (Belgium) (BE)
- Corresponding author
- Garcia, J. Victor
- Venue
- PLOS Pathogens
- Publisher
- Public Library of Science (PLoS)
- Published
- 2015-08-13
- Volume
- 11
- Issue
- 8
- Pages
- e1005075
- ISSN
- 1553-7366 (ISSN-L)
- 1553-7374
- PMC
- PMC4536200
- OpenAlex
- W2143055379
- Cited by
- 77
- References
- 49
- Citations by year
- 2025: 4 · 2024: 2 · 2023: 3 · 2022: 4 · 2021: 7 · 2020: 6 · 2019: 8 · 2018: 8 · 2017: 13 · 2016: 17 · 2015: 5
- FWCI
- 11.14
- Type
- journal article
- Language
- en
- Update notices
- correction (2015-10-16)
- Open access
- gold
- doi.org
- Licence
- Locations
- PLoS Pathogens (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Creighton Digital Repository (CDR) (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Figshare (submittedVersion, cc-by)
- Funders
- University of Nebraska-Lincoln
- National Institutes of Health (UL1TR001111, UL1TR002489)
- Center for AIDS Research, University of Washington (P30 AI-50410)
- University of North Carolina at Chapel Hill (UL1TR001111, P30AI50410)
- Japan Society for the Promotion of Science
- National Institute of Allergy and Infectious Diseases (R01AI096138, R01AI073146, R15AI118550, P30 AI50410, R01AI117740, R56AI095115, P30AI050410)
- National Institute of Environmental Health Sciences (P30ES010126)
- National Center for Advancing Translational Sciences
- Center for AIDS Research, University of North Carolina at Chapel Hill (P30 AI‐50410)
- North Carolina Translational and Clinical Sciences Institute, University of North Carolina at Chapel Hill (UL1TR001111)
- Topics
- Health Sciences › Medicine › Infectious Diseases › HIV/AIDS Research and Interventions
- Health Sciences › Medicine › Infectious Diseases › HIV/AIDS drug development and treatment
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
- Keywords
- rilpivirine, HIV prevention, nanoformulations, PLGA nanoparticles, thermosensitive hydrogel, nanoparticle suspensions, intramuscular administration, pre-exposure prophylaxis, long-acting antiretroviral therapy, reverse transcriptase inhibitors, transmitted/founder virus
- MeSH terms
- Rilpivirine, Animals, Chromatography, High Pressure Liquid, Disease Models, Animal, HeLa Cells, Humans, Vaginal Creams, Foams, and Jellies, HIV Infections, Anti-HIV Agents, Mice, Nanoparticles
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