Evidence map›Paper›PMID 19487423›Full record

ArticleThe Journal of experimental medicine2009

The first T cell response to transmitted/founder virus contributes to the control of acute viremia in HIV-1 infection.

Nilu Goonetilleke, Michael K P Liu, Jesus F Salazar-Gonzalez, Guido Ferrari, Elena Giorgi, Vitaly V Ganusov, Brandon F Keele, Gerald H Learn, Emma L Turnbull, Maria G Salazar and 14 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03980665 (The Effect of Arsenic Trioxide on Eliminating HIV-1 Reservoir Combined With cART), which is not on this map. Cited by 435 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
435citing papers in PubMed, 1 pooled it
24.1field-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.

NCT03980665 phase1unknown statusnot on this mapstarted 2019, after this paper: background citation

The Effect of Arsenic Trioxide on Eliminating HIV-1 Reservoir Combined With cART

TypeinterventionalSponsorGuangzhou 8th People's HospitalRan2019 to 2025Enrolled20ConditionsHIV/AIDSArmsArsenic Trioxide
3 · Its place in the literature

Who cites it

435 citing papers in PubMed, 1 synthesis or guideline pooled it, 641 citations in OpenAlex.

  1. Transcriptional insights into the CD8Journal of translational medicine · 2020
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375 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

24 authors at 8 institutions in 2 countries.

Nilu GoonetillekeMedical Research Council Human Immunology Unit, Weatherall Institute of Molecular Medicine, Oxford University, Oxford OX3 9DS, England, UK.
Michael K P Liu
Jesus F Salazar-Gonzalez
Guido Ferrari
Elena Giorgi
Vitaly V Ganusov
Brandon F Keele
Gerald H Learn
Emma L Turnbull
Maria G Salazar
Kent J Weinhold
Stephen Moore
CHAVI Clinical Core B
Norman Letvin
Barton F Haynes
Myron S Cohen
Peter Hraber
Tanmoy Bhattacharya
Persephone Borrow
Alan S Perelson
Beatrice H Hahn
George M Shaw
Bette T Korber
Andrew J McMichael
Los Alamos National Laboratory · USUniversity of Alabama at Birmingham · USUniversity of Oxford · GBDuke University · USHarvard University · USJenner Institute · GBMRC Human Immunology Unit · GBUniversity of North Carolina at Chapel Hill · US

Funding

HIV IN SEMEN-EFFECTS OF STDS AND ANTIVIRAL THERAPYR37DK049381 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI COHEN, MYRON SCOTT · 2005 to 2014
$3.4M
HIV IN SEMEN--EFFECTS OF STDS AND ANTIVIRAL THERAPYR01DK049381 · NIDDK · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI COHEN, MYRON S · 1996 to 2004
$2.2M
Medical Research Council MC_U137884177NIDDK NIH HHS DK049381NIDDK NIH HHS R01 DK049381NIDDK NIH HHS R37 DK049381PHS HHS A1067854-03
6 · The paper itself

Abstract

Identification of the transmitted/founder virus makes possible, for the first time, a genome-wide analysis of host immune responses against the infecting HIV-1 proteome. A complete dissection was made of the primary HIV-1-specific T cell response induced in three acutely infected patients. Cellular assays, together with new algorithms which identify sites of positive selection in the virus genome, showed that primary HIV-1-specific T cells rapidly select escape mutations concurrent with falling virus load in acute infection. Kinetic analysis and mathematical modeling of virus immune escape showed that the contribution of CD8 T cell-mediated killing of productively infected cells was earlier and much greater than previously recognized and that it contributed to the initial decline of plasma virus in acute infection. After virus escape, these first T cell responses often rapidly waned, leaving or being succeeded by T cell responses to epitopes which escaped more slowly or were invariant. These latter responses are likely to be important in maintaining the already established virus set point. In addition to mutations selected by T cells, there were other selected regions that accrued mutations more gradually but were not associated with a T cell response. These included clusters of mutations in envelope that were targeted by NAbs, a few isolated sites that reverted to the consensus sequence, and bystander mutations in linkage with T cell-driven escape.

Indexed as

HIV-1Viral ProteinsAmino Acid SequenceCytokinesEpitopesEvolution, MolecularGenome, ViralHIV InfectionsHumansImmune SystemModels, TheoreticalMolecular Sequence DataMutationSequence Analysis, ProteinT-LymphocytesViremiaCytokinesEpitopesViral Proteins

Identifiers

PMID19487423
PMCPMC2715063
OpenAlexW2152534166

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.