Evidence map›Paper›PMID 20696836›Full record

ArticleInfection and immunity2010

Trypanosoma cruzi-induced activation of functionally distinct αβ and γδ CD4- CD8- T cells in individuals with polar forms of Chagas' disease.

Fernanda Nobre Amaral Villani, Manoel Otávio da Costa Rocha, Maria do Carmo Pereira Nunes, Lis Ribeiro do Valle Antonelli, Luisa Mourão Dias Magalhães, Janete Soares Coelho dos Santos, Kenneth J Gollob, Walderez O Dutra

Abstract read
In one paragraph

Article in Infection and immunity, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

26 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
  2. Double negative T cells (CD4Frontiers in immunology · 2026
    Article
  3. Article
  4. Blocking activation of CD4Clinical immunology (Orlando, Fla.) · 2023
    Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Distinct CD4Frontiers in immunology · 2021
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Specific activation of CD4Clinical and experimental immunology · 2017
    Article
  18. Low Double-Negative CD3Frontiers in immunology · 2016
    Article
  19. Article
  20. Review
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

8 authors.

Fernanda Nobre Amaral VillaniDepartment of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Manoel Otávio da Costa Rocha
Maria do Carmo Pereira Nunes
Lis Ribeiro do Valle Antonelli
Luisa Mourão Dias Magalhães
Janete Soares Coelho dos Santos
Kenneth J Gollob
Walderez O Dutra

Funding

The role of CD28- cells in human Chagas' diseaseR03AI066044 · NIAID · UNIVERSIDADE FEDERAL DE MINAS GERAIS · PI DUTRA, WALDEREZ O. · 2007 to 2009
$160k
NIAID NIH HHS R03 AI066044
6 · The paper itself

Abstract

CD4(-) CD8(-) (double-negative [DN]) T cells have recently been shown to display important immunological functions in human diseases. They express γδ or αβ T-cell receptors that recognize lipid/glycolipid antigens presented via the nonclassical major histocompatibility complex molecules of the CD1 family. We recently demonstrated that while αβ DN T cells serve primarily to express inflammatory cytokines, γδ DN T cells express mainly interleukin-10 (IL-10) in patients with cutaneous leishmaniasis. We also demonstrated a correlation between DN T cells and the expression of gamma interferon in the acute phase of Trypanosoma cruzi experimental infection. In this work, we sought to investigate whether αβ or γδ DN T cells display distinct immunoregulatory potentials in patients with polar forms of human Chagas' disease. Our data showed that in vitro infection with T. cruzi leads to expansion of DN T cells in patients with the indeterminate and severe cardiac clinical forms of the disease. However, while αβ DN T cells primarily produce inflammatory cytokines in both forms of the disease, γδ DN T cells display a marked, significant increase in antigen-specific IL-10 expression in indeterminate patients relative to cardiac patients. Finally, higher frequencies of the IL-10-producing γδ DN T cells were correlated with improved clinical measures of cardiac function in the patients, suggesting a protective role for these cells in Chagas' disease. Taken together, these data show distinct functional characteristics for αβ and γδ DN T cells associated with distinct morbidity rates and clinical forms in human Chagas' disease.

Indexed as

AdultAgedChagas DiseaseCross-Sectional StudiesFemaleGene Expression RegulationHumansInterleukin-10MaleMiddle AgedReceptors, Antigen, T-Cell, alpha-betaReceptors, Antigen, T-Cell, gamma-deltaTrypanosoma cruziYoung AdultInterleukin-10Receptors, Antigen, T-Cell, alpha-betaReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID20696836
PMCPMC2950361

What OpenQuestion holds

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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.