Evidence map›Paper›PMID 23589672›Full record

Trial reportBlood2013

Interleukin-7 promotes HIV persistence during antiretroviral therapy.

Claire Vandergeeten, Rémi Fromentin, Sandrina DaFonseca, Mariam B Lawani, Irini Sereti, Michael M Lederman, Moti Ramgopal, Jean-Pierre Routy, Rafick-Pierre Sékaly, Nicolas Chomont

2 registry-linked trialsOpen access · greenAbstract readClinical Trial, Phase IRandomized Controlled Trial
In one paragraph

Trial report in Blood, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 159 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
159citing papers in PubMed, 2 pooled it
9.3field-weighted citation impact, top 1% 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.

NCT00099671 phase1completednot on this map

A Phase I, Randomized, Placebo-Controlled, Double-Blind Study Evaluating the Safety of Subcutaneous Single Dose Interleukin-7 in HIV-1-Infected Subjects Who Are Receiving Antiretroviral Treatment

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2005 to 2007Enrolled25ConditionsHIV InfectionsArmsRecombinant human interleukin-7
NCT02563509 phase1completednot on this mapstarted 2016, after this paper: background citation

Reconstitution of HIV-specific Immunity Against HIV

TypeinterventionalSponsorGuangzhou 8th People's HospitalRan2016 to 2017Enrolled30ConditionsHIVArmsHIV-specific CD8 cells
3 · Its place in the literature

Who cites it

159 citing papers in PubMed, 2 syntheses or guidelines pooled it, 246 citations in OpenAlex.

  1. Pooled it
  2. The Hitchhiker Guide to CD4Frontiers in immunology · 2021
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99 more citing papers are in PubMed but not listed here.

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

10 authors at 5 institutions in 2 countries.

Claire VandergeetenVaccine and Gene Therapy Institute Florida, Port St. Lucie, FL 34987, USA.
Rémi Fromentin
Sandrina DaFonseca
Mariam B Lawani
Irini Sereti
Michael M Lederman
Moti Ramgopal
Jean-Pierre Routy
Rafick-Pierre Sékaly
Nicolas Chomont
Vaccine & Gene Therapy Institute of Florida · USCase Western Reserve University · USMcGill University Health Centre · CAMidway College · USNational Institute of Allergy and Infectious Diseases · US

Funding

Viral reservoirs and sanctuaries in HAART - treated patients: role and mechanismsU19AI096109 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI STEVENSON, MARIO · 2011 to 2015
$29.5M
Immunopathogenic Mechanisms of Human Immunodeficiency Virus (HIV) DiseaseZIAAI001121 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI SERETI, IRINI · 2010 to 2025
$27.2M
Novel Concepts for the Eradication of HIVDP1DA028871 · NIDA · VGTI FLORIDA · PI SEKALY, RAFICK PIERRE · 2009 to 2013
$4.5M
CIHR HOP 103230Intramural NIH HHSNIAID NIH HHS 1U19AI096109NIAID NIH HHS U19 AI096109NIDA NIH HHS DP1 DA028871
6 · The paper itself

Abstract

HIV persists in latently infected memory CD4(+) T cells during antiretroviral therapy (ART). When administered to HIV-infected subjects receiving suppressive ART, interleukin-7 (IL-7) increases the number of CD4(+) T cells by promoting their survival and proliferation. However, little is known about the impact of IL-7 on HIV persistence during ART. By isolating large numbers of CD4(+) T cells from HIV-infected subjects, we demonstrate that IL-7 enhances viral production in productively infected cells but does not disrupt viral latency in latently infected cells. When administered to virally suppressed subjects, IL-7 led to the rapid proliferation of memory CD4(+) T cells, which resulted in a 70% increase in the absolute number of circulating CD4(+) T cells harboring integrated HIV DNA 4 weeks after therapy. The genetic diversity of the viral reservoir increased transiently in the majority of the subjects studied before returning to baseline values. Altogether, our results indicate that IL-7 promotes the mechanisms of HIV persistence during ART by enhancing residual levels of viral production and inducing proliferation of latently infected cells, and suggest that IL-7 does not represent a suitable candidate therapeutic strategy for HIV eradication. This trial was registered at www.clinicaltrials.gov as #NCT00099671 (AIDS Clinical Trials Group protocol 5214).

Indexed as

Anti-Retroviral AgentsCD4-Positive T-LymphocytesCell DivisionCells, CulturedGenetic VariationHIV-1HIV InfectionsHumansImmune ToleranceImmunologic MemoryInterleukin-7Virus LatencyAnti-Retroviral AgentsIL7 protein, humanInterleukin-7

Identifiers

PMID23589672
PMCPMC3663425
OpenAlexW1978674283

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.