Evidence map›Paper›PMID 34762600›Full record

Trial reportThe Journal of clinical investigation2022

Anti-HIV antibody development up to 1 year after antiretroviral therapy initiation in acute HIV infection.

Julie L Mitchell, Justin Pollara, Kenneth Dietze, R Whitney Edwards, Junsuke Nohara, Kombo F N'guessan, Michelle Zemil, Supranee Buranapraditkun, Hiroshi Takata, Yifan Li and 26 more

Open access · hybridAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in The Journal of clinical investigation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Trial
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  6. Activation of CXCR3Journal of virology · 2025
    Article
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  10. iScience · 2023
    Article
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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

36 authors at 9 institutions in 3 countries.

Julie L MitchellVaccine and Gene Therapy Institute, Oregon Health and Science University, Beaverton, Oregon, USA.
Justin PollaraDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, USA.
Kenneth DietzeUS Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
R Whitney EdwardsDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, USA.
Junsuke NoharaDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, USA.
Kombo F N'guessanUS Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Michelle ZemilUS Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Supranee BuranapraditkunUS Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Hiroshi TakataVaccine and Gene Therapy Institute, Oregon Health and Science University, Beaverton, Oregon, USA.
Yifan LiUS Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Roshell MuirDepartment of Medicine, Division of Infectious Diseases and HIV Medicine, Drexel University, Philadelphia, Pennsylvania, USA.
Eugene KroonInstitute of HIV Research and Innovation (IHRI), Bangkok, Thailand.
Suteeraporn PinyakornUS Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Shalini JhaDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, USA.
Sopark ManasnayakornDepartment of Medicine and.
Suthat ChottanapundBamrasnaradura Infectious Disease Institute, Nonthaburi, Thailand.
Pattarawat ThantiworasitCenter of Excellence in Vaccine Research and Development, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Peeriya PrueksakaewInstitute of HIV Research and Innovation (IHRI), Bangkok, Thailand.
Nisakorn RatnaratornInstitute of HIV Research and Innovation (IHRI), Bangkok, Thailand.
Bessara NuntapinitArmed Forces Research Institute of Medical Sciences in Bangkok, Bangkok, Thailand.
Lawrence FoxDivision of AIDS, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda, Maryland, USA.
Sodsai TovanabutraUS Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Dominic Paquin-ProulxUS Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Lindsay WieczorekUS Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Victoria R PolonisHenry M. Jackson Foundation for the Advancement of Military Medicine Inc., Bethesda, Maryland, USA.
Frank MaldarelliHIV Dynamics and Replication Program, National Cancer Institute (NCI), NIH, Frederick, Maryland, USA.
Elias K HaddadDepartment of Medicine, Division of Infectious Diseases and HIV Medicine, Drexel University, Philadelphia, Pennsylvania, USA.
Praphan PhanuphakInstitute of HIV Research and Innovation (IHRI), Bangkok, Thailand.
Carlo P SacdalanInstitute of HIV Research and Innovation (IHRI), Bangkok, Thailand.
Morgane RollandUS Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Nittaya PhanuphakInstitute of HIV Research and Innovation (IHRI), Bangkok, Thailand.
Jintanat AnanworanichUS Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Sandhya VasanUS Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Guido FerrariDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, USA.
Lydie TrautmannVaccine and Gene Therapy Institute, Oregon Health and Science University, Beaverton, Oregon, USA.
RV254 and RV304 Study Groups
Henry M. Jackson Foundation · USHIV Netherlands Australia Thailand Research Collaboration · THDuke Medical Center · USDrexel University · USArmed Forces Research Institute of Medical Science · THBamrasnaradura Infectious Diseases Institute · THCenter for Cancer Research · USChulalongkorn University · THNational Institute of Allergy and Infectious Diseases · US

Funding

Social and Behavioral Sciences CoreP30AI064518 · NIAID · DUKE UNIVERSITY · PI GEORGIA Doris TOMARAS · 2005 to 2026
$50.5M
Clinical Interventional Studies of HIV ReservoirsZIABC011464 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MALDARELLI, FRANK · 2012 to 2025
$13.2M
HIV-1 Genetic Variation in Infected IndividualsZIABC010819 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MALDARELLI, FRANK · 2009 to 2025
$9.9M
Preservation of adaptive immunity leads to HIV control upon treatment cessation.R01AI108433 · NIAID · VGTI FLORIDA · PI VASAN, SANDHYA · 2014 to 2018
$3.6M
Combined Hepatitis B and HIV-1 envelope vaccination to augment T cell help via linked recognition of unrelated antigensK01OD024877 · OD · DUKE UNIVERSITY · PI POLLARA, JUSTIN JOSEPH · 2017 to 2019
$1.0M
NIAID NIH HHS P30 AI064518NIAID NIH HHS R01 AI108433NIH HHS K01 OD024877
6 · The paper itself

Abstract

Early initiation of antiretroviral therapy (ART) in acute HIV infection (AHI) is effective at limiting seeding of the HIV viral reservoir, but little is known about how the resultant decreased antigen load affects long-term Ab development after ART. We report here that Env-specific plasma antibody (Ab) levels and Ab-dependent cellular cytotoxicity (ADCC) increased during the first 24 weeks of ART and correlated with Ab levels persisting after 48 weeks of ART. Participants treated in AHI stage 1 had lower Env-specific Ab levels and ADCC activity on ART than did those treated later. Importantly, participants who initiated ART after peak viremia in AHI developed elevated cross-clade ADCC responses that were detectable 1 year after ART initiation, even though clinically undetectable viremia was reached by 24 weeks. These data suggest that there is more germinal center (GC) activity in the later stages of AHI and that Ab development continues in the absence of detectable viremia during the first year of suppressive ART. The development of therapeutic interventions that can enhance earlier development of GCs in AHI and Abs after ART initiation could provide important protection against the viral reservoir that is seeded in individuals treated early in the disease.

Indexed as

Acute DiseaseAdultAnti-Retroviral AgentsCell LineFemaleHIV-1HIV AntibodiesHIV InfectionsHumansMaleViremiaAnti-Retroviral AgentsHIV AntibodiesAIDS/HIVImmunoglobulinsImmunology

Identifiers

PMID34762600
PMCPMC8718150
OpenAlexW3211986893

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.