Author
Listed:
- Xiao L. Chang
(Vaccine & Gene Therapy Institute
Oregon Health & Science University)
- Gabriela M. Webb
(Vaccine & Gene Therapy Institute
Oregon Health & Science University)
- Helen L. Wu
(Vaccine & Gene Therapy Institute
Oregon Health & Science University)
- Justin M. Greene
(Vaccine & Gene Therapy Institute)
- Shaheed Abdulhaqq
(Vaccine & Gene Therapy Institute)
- Katherine B. Bateman
(Vaccine & Gene Therapy Institute)
- Jason S. Reed
(Vaccine & Gene Therapy Institute)
- Cleiton Pessoa
(Vaccine & Gene Therapy Institute)
- Whitney C. Weber
(Vaccine & Gene Therapy Institute)
- Nicholas Maier
(Vaccine & Gene Therapy Institute)
- Glen M. Chew
(University of Hawaii)
- Roxanne M. Gilbride
(Vaccine & Gene Therapy Institute)
- Lina Gao
(Oregon Health & Science University)
- Rebecca Agnor
(Oregon Health & Science University)
- Travis Giobbi
(Oregon Health & Science University)
- Jeffrey Torgerson
(Oregon Health & Science University)
- Don Siess
(Oregon Health & Science University)
- Nicole Burnett
(Oregon Health & Science University)
- Miranda Fischer
(Oregon Health & Science University)
- Oriene Shiel
(Oregon Health & Science University)
- Cassandra Moats
(Oregon Health & Science University)
- Bruce Patterson
(IncellDX)
- Kush Dhody
(Amarex Clinical Research LLC)
- Scott Kelly
(CytoDyn Inc.)
- Nader Pourhassan
(CytoDyn Inc.)
- Diogo M. Magnani
(MassBiologics of the University of Massachusetts Medical School)
- Jeremy Smedley
(Oregon Health & Science University)
- Benjamin N. Bimber
(Vaccine & Gene Therapy Institute
Oregon Health & Science University)
- Nancy L. Haigwood
(Vaccine & Gene Therapy Institute)
- Scott G. Hansen
(Vaccine & Gene Therapy Institute)
- Timothy R. Brown
(Palm Springs)
- Lishomwa C. Ndhlovu
(Weill Cornell Medicine)
- Jonah B. Sacha
(Vaccine & Gene Therapy Institute
Oregon Health & Science University)
Abstract
In the absence of a prophylactic vaccine, the use of antiretroviral therapy (ART) as pre-exposure prophylaxis (PrEP) to prevent HIV acquisition by uninfected individuals is a promising approach to slowing the epidemic, but its efficacy is hampered by incomplete patient adherence and ART-resistant variants. Here, we report that competitive inhibition of HIV Env-CCR5 binding via the CCR5-specific antibody Leronlimab protects rhesus macaques against infection following repeated intrarectal challenges of CCR5-tropic SHIVSF162P3. Injection of Leronlimab weekly at 10 mg/kg provides significant but partial protection, while biweekly 50 mg/kg provides complete protection from SHIV acquisition. Tissue biopsies from protected macaques post challenge show complete CCR5 receptor occupancy and an absence of viral nucleic acids. After Leronlimab washout, protected macaques remain aviremic, and adoptive transfer of hematologic cells into naïve macaques does not transmit viral infection. These data identify CCR5 blockade with Leronlimab as a promising approach to HIV prophylaxis and support initiation of clinical trials.
Suggested Citation
Xiao L. Chang & Gabriela M. Webb & Helen L. Wu & Justin M. Greene & Shaheed Abdulhaqq & Katherine B. Bateman & Jason S. Reed & Cleiton Pessoa & Whitney C. Weber & Nicholas Maier & Glen M. Chew & Roxan, 2021.
"Antibody-based CCR5 blockade protects Macaques from mucosal SHIV transmission,"
Nature Communications, Nature, vol. 12(1), pages 1-11, December.
Handle:
RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-23697-6
DOI: 10.1038/s41467-021-23697-6
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