Author
Listed:
- Samuel J. Vidal
(Harvard Medical School
Harvard Medical School)
- Elena Bekerman
(Gilead Sciences)
- Derek Hansen
(Gilead Sciences)
- Bing Lu
(Gilead Sciences)
- Kelly Wang
(Gilead Sciences)
- Judy Mwangi
(Gilead Sciences)
- William Rowe
(Gilead Sciences)
- Federico Campigotto
(Gilead Sciences)
- Jim Zheng
(Gilead Sciences)
- Darryl Kato
(Gilead Sciences)
- Abishek Chandrashekar
(Harvard Medical School)
- Julia Barrett
(Harvard Medical School)
- Shivani Patel
(Harvard Medical School)
- Huahua Wan
(Harvard Medical School)
- Tochi Anioke
(Harvard Medical School)
- Noe B. Mercado
(Harvard Medical School)
- Joseph P. Nkolola
(Harvard Medical School)
- Melissa J. Ferguson
(Alpha Genesis, Inc.)
- William J. Rinaldi
(Alpha Genesis, Inc.)
- Christian Callebaut
(Gilead Sciences)
- Wade Blair
(Gilead Sciences)
- Tomas Cihlar
(Gilead Sciences)
- Romas Geleziunas
(Gilead Sciences)
- Stephen R. Yant
(Gilead Sciences)
- Dan H. Barouch
(Harvard Medical School
Ragon Institute of MGH, MIT and Harvard)
Abstract
Because no currently available vaccine can prevent HIV infection, pre-exposure prophylaxis (PrEP) with antiretrovirals (ARVs) is an important tool for combating the HIV pandemic1,2. Long-acting ARVs promise to build on the success of current PrEP strategies, which must be taken daily, by reducing the frequency of administration3. GS-CA1 is a small-molecule HIV capsid inhibitor with picomolar antiviral potency against a broad array of HIV strains, including variants resistant to existing ARVs, and has shown long-acting therapeutic potential in a mouse model of HIV infection4. Here we show that a single subcutaneous administration of GS-CA1 provides long-term protection against repeated rectal simian–human immunodeficiency virus (SHIV) challenges in rhesus macaques. Whereas all control animals became infected after 15 weekly challenges, a single 300 mg kg−1 dose of GS-CA1 provided per-exposure infection risk reduction of 97% for 24 weeks. Pharmacokinetic analysis showed a correlation between GS-CA1 plasma concentration and protection from SHIV challenges. GS-CA1 levels greater than twice the rhesus plasma protein-adjusted 95% effective concentration conferred 100% protection in this model. These proof-of-concept data support the development of capsid inhibitors as a novel long-acting PrEP strategy in humans.
Suggested Citation
Samuel J. Vidal & Elena Bekerman & Derek Hansen & Bing Lu & Kelly Wang & Judy Mwangi & William Rowe & Federico Campigotto & Jim Zheng & Darryl Kato & Abishek Chandrashekar & Julia Barrett & Shivani Pa, 2022.
"Long-acting capsid inhibitor protects macaques from repeat SHIV challenges,"
Nature, Nature, vol. 601(7894), pages 612-616, January.
Handle:
RePEc:nat:nature:v:601:y:2022:i:7894:d:10.1038_s41586-021-04279-4
DOI: 10.1038/s41586-021-04279-4
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