Evidence map›Paper›PMID 15937547›Full record

Trial reportThe Journal of clinical investigation2005

In vivo expansion of CD4CD45RO-CD25 T cells expressing foxP3 in IL-2-treated HIV-infected patients.

Irini Sereti, Hiromi Imamichi, Ven Natarajan, Tomozumi Imamichi, Meena S Ramchandani, Yunden Badralmaa, Steve C Berg, Julia A Metcalf, Barbara K Hahn, Jean M Shen and 5 more

Open access · bronzeAbstract readClinical TrialClinical Trial, Phase III
In one paragraph

Trial report in The Journal of clinical investigation, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
6.6field-weighted citation impact, top 2% 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

52 citing papers in PubMed, 119 citations in OpenAlex.

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  19. Interleukin 15 provides relief to CTLs from regulatory T cell-mediated inhibition: implications for adoptive T cell-based therapies for lymphoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2013
    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

15 authors at 1 institution in 1 country.

Irini SeretiNational Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD 20892, USA. isereti@niaid.nih.gov
Hiromi Imamichi
Ven Natarajan
Tomozumi Imamichi
Meena S Ramchandani
Yunden Badralmaa
Steve C Berg
Julia A Metcalf
Barbara K Hahn
Jean M Shen
April Powers
Richard T Davey
Joseph A Kovacs
Ethan M Shevach
H Clifford Lane
National Institute of Allergy and Infectious Diseases · US

Funding

Immunologic/Virologic Approaches To HIV-1 TherapeuticsZ01AI000865 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI DAVEY, RICHARD · 2000 to 2008
$4.6M
PATHOGENIC MECHANISMS IN HUMAN IMMUNODEFICIENCY VIRUS INFECTIONSZ01AI000585 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI LANE, HENRY C · 1990 to 2008
$4.5M
RECEPTORS, CORECEPTORS, AND COUNTER RECEPTORS IN T CELL ACTIVATIONZ01AI000224 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI SHEVACH, ETHAN M. · 1985 to 2008
$3.5M
NCI NIH HHS N01 CO012400NCI NIH HHS N01-CO-12400
6 · The paper itself

Abstract

Administration of IL-2 to HIV-infected patients leads to expansion of a unique subset of CD4CD45ROCD25 cells. In this study, the origin, clonality, and function of these cells were investigated. Analysis of TCR excision circles revealed that the CD4CD45ROCD25 cells were the product of peripheral expansion but remained polyclonal as determined by TCR repertoire analysis. Phenotypically, these cells were distinct from naturally occurring Tregs; they exhibited intermediate features, between those of memory and naive cells, and had lower susceptibility to apoptosis than CD45ROCD25 or memory T cells. Studies of intracellular cytokine production and proliferation revealed that cytokine-expanded naive CD25 cells had low IL-2 production and required costimulation for proliferation. Despite elevated expression of forkhead transcription factor P3 (foxP3), they exerted only weak suppression compared with CD45ROCD25 cells (Tregs). In summary, in vivo IL-2 administration to HIV-infected patients leads to peripheral expansion of a population of long-lived CD4CD45ROCD25 cells that express high levels of foxP3 but exert weak suppressive function. These CD4CD25 cytokine-expanded naive cells, distinct from antigen-triggered cells and Tregs, play a role in the maintenance of a state of low turnover and sustained expansion of the CD4 T cell pool.

Indexed as

AdultApoptosisCD4-Positive T-LymphocytesCell ProliferationCohort StudiesDNA-Binding ProteinsFollow-Up StudiesForkhead Transcription FactorsGene ExpressionHIV InfectionsHumansImmunologic MemoryInterleukin-2Leukocyte Common AntigensMiddle AgedPhenotypeDNA-Binding ProteinsForkhead Transcription FactorsFOXP3 protein, humanInterleukin-2Leukocyte Common AntigensReceptors, Interleukin-2Recombinant Proteins

Identifiers

PMID15937547
PMCPMC1142113
OpenAlexW2143161686

What OpenQuestion holds

Textmetadata
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.