Evidence map›Paper›PMID 35452496›Full record

ArticlePLoS pathogens2022

HIV envelope antibodies and TLR7 agonist partially prevent viral rebound in chronically SHIV-infected monkeys.

Brian Moldt, Abishek Chandrashekar, Erica N Borducchi, Joseph P Nkolola, Heather Stephenson, Mark Nagel, Magdeleine Hung, Joshua Goldsmith, Craig S Pace, Brian Carr and 4 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.1field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 32 citations in OpenAlex.

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  10. Post-intervention control in HIV immunotherapy trials.Current opinion in HIV and AIDS · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 1 country.

Brian MoldtGilead Sciences, Foster City, California, United States of America.
Abishek ChandrashekarBeth Israel Deaconess Medical Center, Boston, Massachusetts, United States of America.
Erica N BorducchiBeth Israel Deaconess Medical Center, Boston, Massachusetts, United States of America.
Joseph P NkololaBeth Israel Deaconess Medical Center, Boston, Massachusetts, United States of America.
Heather StephensonGilead Sciences, Foster City, California, United States of America.
Mark NagelGilead Sciences, Foster City, California, United States of America.
Magdeleine HungGilead Sciences, Foster City, California, United States of America.
Joshua GoldsmithGilead Sciences, Foster City, California, United States of America.
Craig S PaceGilead Sciences, Foster City, California, United States of America.
Brian CarrGilead Sciences, Foster City, California, United States of America.
Nathan D ThomsenGilead Sciences, Foster City, California, United States of America.
Wade S BlairGilead Sciences, Foster City, California, United States of America.
Romas GeleziunasGilead Sciences, Foster City, California, United States of America.
Dan H BarouchBeth Israel Deaconess Medical Center, Boston, Massachusetts, United States of America.ORCID 0000-0001-5127-4659
Gilead Sciences (United States) · USBeth Israel Deaconess Medical Center · US

Funding

Project 2U19AI128751 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BAROUCH, DAN H. · 2018 to 2022
$14.0M
NIAID NIH HHS U19 AI128751
6 · The paper itself

Abstract

A key challenge for the development of a cure to HIV-1 infection is the persistent viral reservoir established during early infection. Previous studies using Toll-like receptor 7 (TLR7) agonists and broadly neutralizing antibodies (bNAbs) have shown delay or prevention of viral rebound following antiretroviral therapy (ART) discontinuation in simian-human immunodeficiency virus (SHIV)-infected rhesus macaques. In these prior studies, ART was initiated early during acute infection, which limited the size and diversity of the viral reservoir. Here we evaluated in SHIV-infected rhesus macaques that did not initiate ART until 1 year into chronic infection whether the TLR7 agonist vesatolimod in combination with the bNAb PGT121, formatted either as a human IgG1, an effector enhanced IgG1, or an anti-CD3 bispecific antibody, would delay or prevent viral rebound following ART discontinuation. We found that all 3 antibody formats in combination with vesatolimod were able to prevent viral rebound following ART discontinuation in a subset of animals. These data indicate that a TLR7 agonist combined with antibodies may be a promising strategy to achieve long-term ART-free HIV remission in humans.

Indexed as

HIV-1HIV InfectionsSimian Acquired Immunodeficiency SyndromeSimian Immunodeficiency VirusAnimalsAnti-Retroviral AgentsBroadly Neutralizing AntibodiesHIV AntibodiesImmunoglobulin GMacaca mulattaToll-Like Receptor 7Viral LoadAnti-Retroviral AgentsBroadly Neutralizing AntibodiesHIV AntibodiesImmunoglobulin GToll-Like Receptor 7

Identifiers

PMID35452496
PMCPMC9067686
OpenAlexW4224289637

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.