Evidence map›Paper›PMID 21047964›Full record

ArticleJournal of virology2011

Comprehensive analysis of frequency and phenotype of T regulatory cells in HIV infection: CD39 expression of FoxP3+ T regulatory cells correlates with progressive disease.

Julian Schulze Zur Wiesch, Adriana Thomssen, Philip Hartjen, Ilona Tóth, Clara Lehmann, Dirk Meyer-Olson, Kristina Colberg, Sebastian Frerk, Dalia Babikir, Stefan Schmiedel and 10 more

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed
7.0field-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

98 citing papers in PubMed, 169 citations in OpenAlex.

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  17. CRISPR/Cas9-Mediated Insertion of HIV Long Terminal Repeat withinJournal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  18. Article
  19. Phenotypic analysis of the pediatric immune response to SARS-CoV-2 by flow cytometry.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2022
    Article
  20. The dark side of Tregs during aging.Frontiers in immunology · 2022
    Review

38 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

20 authors at 7 institutions in 2 countries.

Julian Schulze Zur WieschInfectious Disease Unit, Department of Medicine, University Medical Center Hamburg-Eppendorf, Martinistr. 52, 20246 Hamburg, Germany. julianszw@gmail.com
Adriana Thomssen
Philip Hartjen
Ilona Tóth
Clara Lehmann
Dirk Meyer-Olson
Kristina Colberg
Sebastian Frerk
Dalia Babikir
Stefan Schmiedel
Olaf Degen
Stefan Mauss
Jürgen Rockstroh
Schlomo Staszewski
Pavel Khaykin
Alexander Strasak
Ansgar W Lohse
Gerd Fätkenheuer
Joachim Hauber
Jan van Lunzen
Leibniz Institute of Virology (LIV) · DEUniversity Medical Center Hamburg-Eppendorf · DEGoethe University Frankfurt · DEUniversität Hamburg · DECenter for HIV and Hepatogastroenterology · DEMedizinische Hochschule Hannover · DEStatistics Austria · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There are conflicting data about the frequency and role of regulatory T cells (Tregs) during the course of HIV infection. Peripheral blood of a large cohort of HIV-infected patients (n = 131) at different stages of disease, including 15 long-term nonprogressors and 21 elite controllers, was analyzed to determine the frequency and phenotype of Tregs, defined as CD4(+), CD25(high), CD127(low), FoxP3(high) cells. A significantly increased relative frequency of Tregs within the CD4(+) compartment of HIV(+) patients compared to that of healthy controls (P < 0.0001) was observed. Additionally, the relative frequency of Tregs directly correlated with HIV viral load and inversely with CD4(+) counts. However, the absolute Treg number was reduced in HIV-infected patients versus healthy controls (P < 0.0001), with the exception of elite controllers (P > 0.05). The loss of absolute Treg numbers coincided with rising markers of immune activation (P < 0.0006). The initiation of antiviral therapy significantly increased absolute Treg numbers (P < 0.0031). We find that the expression of CD39, a newly defined ectonucleotidase with immunomodulatory functions on Tregs, correlated with progressive HIV disease, HIV viral load, and immune activation. Of note, when tested in peripheral blood mononuclear cells of healthy volunteers, the in vitro capacity to suppress T-cell proliferation was limited to CD4(+), CD25(high), CD39(+) T cells. Interestingly, Tregs of elite controllers exhibited not only the highest expression of CCR5, CTLA-4, and ICOS but also the lowest level of CD39. The data presented here reconcile the seemingly contradictory results of previous studies looking at Tregs in HIV and highlight the complexity of Treg-mediated immunoregulation during human viral infections.

Indexed as

AdultAgedAged, 80 and overAntigens, CDApyraseDisease ProgressionFemaleForkhead Transcription FactorsHIV InfectionsHumansMaleMiddle AgedT-Lymphocytes, RegulatoryViral LoadAntigens, CDApyraseCD39 antigenForkhead Transcription FactorsFOXP3 protein, human

Identifiers

PMID21047964
PMCPMC3020516
OpenAlexW2119546576

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.