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Completed NON-SBIR/STTR RPGS NIH (US)

STudy of Acute HIV for investiGating Eradication Strategies (STAGES)

$7.94M USD

Funder NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
Recipient Organization University of California, San Francisco
Country United States
Start Date Aug 01, 2024
End Date Jul 31, 2025
Duration 364 days
Number of Grantees 3
Roles Co-Investigator; Principal Investigator
Data Source NIH (US)
Grant ID 11118300
Grant Description

PROJECT SUMMARY/ ABSTRACT The goal of HIV cure research is to induce “antiretroviral therapy (ART)-free” remission by eliminating persistent HIV to overcome the need for lifelong ART and improve clinical outcomes associated with persistent HIV (increased inflammation- and aging-associated diseases). However, HIV cure trials have thus far failed to

demonstrate a clinically meaningful reduction in the HIV reservoir size or lead to sustained ART-free viral control. The goal of the proposed work is to address a critical need – to determine host in vivo mechanisms that drive HIV reservoir decay and sustain long-term viral control, identifying potential novel therapeutic candidates for HIV

cure. We recently demonstrated that class II cytokines (specifically, IL-10 and type I and III interferons) exhibited ongoing fluctuations and predicted faster HIV reservoir decay during the first 24 weeks of ART. These data support prior work demonstrating a dynamic and temporal role of type I interferons in controlling HIV/SIV infection

and two recent studies that showed a critical role for IL-10 in the maintenance of the HIV/SIV reservoir. However, these other studies did not specifically evaluate the role of host cellular drivers of class II cytokine-mediated viral control across HIV stages: acute HIV infection (AHI), ART initiation (ARTi), ART suppression (ART+), and ART

interruption (ATI). Our central hypothesis is that class II cytokines dynamically control virus at different stages of HIV. We aim to identify the host cellular drivers of class II cytokine-mediated viral control across HIV stages from 50 participants from our UCSF Treat Acute HIV cohort (diagnosed and initiated ART

All Grantees

University of California, San Francisco

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