Evidence map›Paper›PMID 21383382›Full record

ArticleThe Journal of infectious diseases2011

Programmed death 1 and cytokine inducible SH2-containing protein dependent expansion of regulatory T cells upon stimulation With Mycobacterium tuberculosis.

Sivakumar Periasamy, Rohan Dhiman, Peter F Barnes, Padmaja Paidipally, Amy Tvinnereim, Anuradha Bandaru, Vijaya Lakshmi Valluri, Ramakrishna Vankayalapati

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

38 citing papers in PubMed, 69 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Frontiers in immunology · 2022
    Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. The promise of CD4Haematologica · 2019
    Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 3 countries.

Sivakumar PeriasamyCenter for Pulmonary and Infectious Disease Control, University of Texas Health Center, Tyler, India.
Rohan Dhiman
Peter F Barnes
Padmaja Paidipally
Amy Tvinnereim
Anuradha Bandaru
Vijaya Lakshmi Valluri
Ramakrishna Vankayalapati
Palo Alto Center for Pulmonary Disease Prevention · USCenter for Disease Control · TWLepra Society · IN

Funding

Regulation of IFN-gamma production in human tuberculosisR01AI063514 · NIAID · UNIVERSITY OF TEXAS HLTH CTR AT TYLER · PI BARNES, PETER F. · 2005 to 2009
$1.3M
The role of NK cells in human M. Tuberculosis infectionR01AI054629 · NIAID · UNIVERSITY OF TEXAS HLTH CTR AT TYLER · PI VANKAYALAPATI, RAMAKRISHNA · 2005 to 2009
$1.3M
The role of regulatory T cells in M. tuberculosis infectionR21AI073612 · NIAID · UNIVERSITY OF TEXAS HLTH CTR AT TYLER · PI VANKAYALAPATI, RAMAKRISHNA · 2008 to 2009
$369k
NIAID NIH HHS AI054629NIAID NIH HHS AI063514NIAID NIH HHS AI073612NIAID NIH HHS R01 AI054629NIAID NIH HHS R01 AI063514NIAID NIH HHS R21 AI073612PHS HHS A1085135
6 · The paper itself

Abstract

We previously found that CD4(+)CD25(+)FoxP3(+) regulatory T cells (Tregs) expand in response to Mycobacterium tuberculosis infection in individuals who are healthy tuberculin reactors, but not in tuberculin-negative individuals. We also found that the M. tuberculosis mannose-capped lipoarabinomannan and prostaglandin E2 produced by monocytes are involved in Treg expansion. In this study, we found that Tregs expanded from CD4(+)CCR4(+) cells but not from CCR4(-) cells. However, introduction of CCR4 small interfering RNA (siRNA) into CD4(+) cells only marginally reduced expansion of Tregs. Using siRNA and neutralizing antibodies, we found that expansion of Tregs by M. tuberculosis required expression of programmed death1 (PD-1) and expression of the signaling molecule, cytokine inducible SH2-containing protein (CISH). Anti-PD-1 siRNA inhibited expression of CISH by expanded Tregs. M. tuberculosis-expanded Tregs produced transforming growth factor β and interleukin 10 and reduced the frequency of interferon γ-producing autologous CD8(+) cells. We conclude that M. tuberculosis infection induces development of Tregs from CCR4(+) cells through a process that depends on PD-1and CISH.

Indexed as

AdolescentAdultAgedAntigens, CDApoptosis Regulatory ProteinsCD4 AntigensHumansMiddle AgedMycobacterium tuberculosisProgrammed Cell Death 1 ReceptorReceptors, CCR4Suppressor of Cytokine Signaling ProteinsT-Lymphocytes, RegulatoryT-Lymphocyte SubsetsTuberculosisYoung AdultAntigens, CDApoptosis Regulatory ProteinsCCR4 protein, humanCD4 AntigensPDCD1 protein, humanProgrammed Cell Death 1 ReceptorReceptors, CCR4Suppressor of Cytokine Signaling Proteins

Identifiers

PMID21383382
PMCPMC3069733
OpenAlexW2148761057

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.