Adeno-associated viral delivery of Env-specific antibodies prevents SIV rebound after discontinuing antiretroviral therapy

An alternative to lifelong antiretroviral therapy (ART) is needed to achieve durable control of HIV-1. Here, we show that adeno-associated virus (AAV) delivery of two rhesus macaque antibodies to the simian immunodeficiency virus (SIV) envelope glycoprotein (Env) with potent neutralization and antibody-dependent cellular cytotoxicity can prevent viral rebound in macaques infected with barcoded SIV<sub>mac</sub>239M after discontinuing suppressive ART. After AAV administration, sustained antibody expression with minimal antidrug antibody responses was achieved in all but one animal. After ART withdrawal, SIV replication rebounded within 2 weeks in all control animals but remained <15 copies per milliliter in plasma for more than a year in four of the eight animals that received AAV vectors encoding Env-specific antibodies. Viral sequences from animals that rebounded with delayed kinetics exhibited restricted clonal diversity and antibody escape mutations in Env. Thus, sustained expression of antibodies with potent antiviral activity can afford durable, ART-free containment of pathogenic SIV infection.

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Publication Details

Journal
Science Immunology
Published
2025-02-28
DOI
https://doi.org/10.1126/sciimmunol.adq4973
Citations
3
Primary Topic
HIV Research and Treatment
Type
article
Field-Weighted Citation Impact
3.11
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article

Adeno-associated viral delivery of Env-specific antibodies prevents SIV rebound after discontinuing antiretroviral therapy

David T. Evans, Christine M. Fennessey, Guangping Gao, Rosemarie D. Mason et al.
3 citations
Science Immunology
HIV Research and Treatment
3.11
article

Adeno-associated viral delivery of Env-specific antibodies prevents SIV rebound after discontinuing antiretroviral therapy

David T. Evans, Christine M. Fennessey, Guangping Gao, Rosemarie D. Mason, Aimee Teo Broman, Jeffrey D. Lifson, Emek Köse, Brandon F. Keele, Natasha M. Clark, Saverio Capuano, Matthew R. Gardner, Taina T. Immonen, Vadim A. Klenchin, Mario Roederer, Nida K. Keles
article en
3 citations

Abstract

An alternative to lifelong antiretroviral therapy (ART) is needed to achieve durable control of HIV-1. Here, we show that adeno-associated virus (AAV) delivery of two rhesus macaque antibodies to the simian immunodeficiency virus (SIV) envelope glycoprotein (Env) with potent neutralization and antibody-dependent cellular cytotoxicity can prevent viral rebound in macaques infected with barcoded SIV<sub>mac</sub>239M after discontinuing suppressive ART. After AAV administration, sustained antibody expression with minimal antidrug antibody responses was achieved in all but one animal. After ART withdrawal, SIV replication rebounded within 2 weeks in all control animals but remained <15 copies per milliliter in plasma for more than a year in four of the eight animals that received AAV vectors encoding Env-specific antibodies. Viral sequences from animals that rebounded with delayed kinetics exhibited restricted clonal diversity and antibody escape mutations in Env. Thus, sustained expression of antibodies with potent antiviral activity can afford durable, ART-free containment of pathogenic SIV infection.

Science ImmunologyVol. 10(104)
National Institutes of Health (US), University of Wisconsin–Madison (US), Emory University (US), University of Massachusetts Chan Medical School (US), Frederick National Laboratory for Cancer Research (US), National Institute of Allergy and Infectious Diseases (US)
Openalex Percentile: Top 10%
HIV Research and Treatment
3.11
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