Evidence map›Paper›PMID 18390743›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2008

CD127 and CD25 expression defines CD4+ T cell subsets that are differentially depleted during HIV infection.

Richard M Dunham, Barbara Cervasi, Jason M Brenchley, Helmut Albrecht, Amy Weintrob, Beth Sumpter, Jessica Engram, Shari Gordon, Nichole R Klatt, Ian Frank and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

59 citing papers in PubMed, 121 citations in OpenAlex.

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  10. Imbalance of circulating CTLA4Clinical and experimental medicine · 2022
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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 5 institutions in 1 country.

Richard M DunhamDepartment of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.
Barbara Cervasi
Jason M Brenchley
Helmut Albrecht
Amy Weintrob
Beth Sumpter
Jessica Engram
Shari Gordon
Nichole R Klatt
Ian Frank
Donald L Sodora
Daniel C Douek
Mirko Paiardini
Guido Silvestri
Emory University · USUniversity of Pennsylvania · USEmory University Hospital Midtown · USNational Institutes of Health · USCenter for Infectious Disease Research · US

Funding

YNPRC NHP CLINICAL MEDICINE RESIDENCY PROGRAM - SUPPLEMENTP51RR000165 · NCRR · EMORY UNIVERSITY · PI JOHNS, MICHAEL M · 1985 to 2011
$114.0M
Studies of Natural SIV Infection of Sooty MangabeysR01AI066998 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI SILVESTRI, GUIDO · 2006 to 2010
$3.5M
Studies of the HIV-associated cell cycle diseaseR01AI052755 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI SILVESTRI, GUIDO · 2003 to 2006
$1.6M
Mechanisms of Immune Activation and Disease Progression in Animal ModelsZ01AI001029 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI BRENCHLEY, JASON · 2008 to 2008
$455k
Intramural NIH HHS Z99 AI999999NCRR NIH HHS P51 RR000165NCRR NIH HHS RR-00165NIAID NIH HHS R01 AI052755NIAID NIH HHS R01 AI066998NIAID NIH HHS R01 AI52755NIAID NIH HHS R01 AI66998
6 · The paper itself

Abstract

Decreased CD4(+) T cell counts are the best marker of disease progression during HIV infection. However, CD4(+) T cells are heterogeneous in phenotype and function, and it is unknown how preferential depletion of specific CD4(+) T cell subsets influences disease severity. CD4(+) T cells can be classified into three subsets by the expression of receptors for two T cell-tropic cytokines, IL-2 (CD25) and IL-7 (CD127). The CD127(+)CD25(low/-) subset includes IL-2-producing naive and central memory T cells; the CD127(-)CD25(-) subset includes mainly effector T cells expressing perforin and IFN-gamma; and the CD127(low)CD25(high) subset includes FoxP3-expressing regulatory T cells. Herein we investigated how the proportions of these T cell subsets are changed during HIV infection. When compared with healthy controls, HIV-infected patients show a relative increase in CD4(+)CD127(-)CD25(-) T cells that is related to an absolute decline of CD4(+)CD127(+)CD25(low/-) T cells. Interestingly, this expansion of CD4(+)CD127(-) T cells was not observed in naturally SIV-infected sooty mangabeys. The relative expansion of CD4(+)CD127(-)CD25(-) T cells correlated directly with the levels of total CD4(+) T cell depletion and immune activation. CD4(+)CD127(-)CD25(-) T cells were not selectively resistant to HIV infection as levels of cell-associated virus were similar in all non-naive CD4(+) T cell subsets. These data indicate that, during HIV infection, specific changes in the fraction of CD4(+) T cells expressing CD25 and/or CD127 are associated with disease progression. Further studies will determine whether monitoring the three subsets of CD4(+) T cells defined based on the expression of CD25 and CD127 should be used in the clinical management of HIV-infected individuals.

Indexed as

HIV-1AdultAnimalsCD4 Lymphocyte CountCD4-Positive T-LymphocytesCercocebus atysDisease ProgressionFemaleHIV InfectionsHumansInterleukin-2 Receptor alpha SubunitInterleukin-7 Receptor alpha SubunitMaleMiddle AgedSimian Acquired Immunodeficiency SyndromeSimian Immunodeficiency VirusInterleukin-2 Receptor alpha SubunitInterleukin-7 Receptor alpha Subunit

Identifiers

PMID18390743
PMCPMC2683429
OpenAlexW1816675776

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.