Evidence map›Paper›PMID 25483139›Full record

ArticleBrain, behavior, and immunity2015

Immunoendocrine dysbalance during uncontrolled T. cruzi infection is associated with the acquisition of a Th-1-like phenotype by Foxp3(+) T cells.

Florencia B González, Silvina R Villar, Rodrigo Fernández Bussy, Gaëlle H Martin, Louis Pérol, Romina Manarin, Silvana V Spinelli, Caroline Pilon, José Laurent Cohen, Oscar A Bottasso and 2 more

Open access · greenAbstract read
In one paragraph

Article in Brain, behavior, and immunity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 10% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Dynamics and functional heterogeneity of FOXP3+ regulatory T cells in Trypanosoma cruzi infection: a systematic review.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Pooled it
  2. T cell exhaustion in parasitic infections.Frontiers in immunology · 2026
    Review
  3. Towards a map of the immune system manipulation network byFrontiers in cellular and infection microbiology · 2025
    Review
  4. Article
  5. Nasal vaccination againstFrontiers in immunology · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Infection-Associated Thymic Atrophy.Frontiers in immunology · 2021
    Review
  11. Review
  12. Review
  13. Article
  14. Limited Foxp3Frontiers in immunology · 2018
    Article
  15. Review
  16. Article
  17. Article
  18. Benznidazole affects expression of Th1, Th17 and Treg cytokines during acute experimentalThe journal of venomous animals and toxins including tropical diseases · 2017
    Article
  19. Unconventional Pro-inflammatory CD4Frontiers in immunology · 2017
    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

12 authors at 6 institutions in 2 countries.

Florencia B GonzálezIDICER-CONICET, Institute of Clinical and Experimental Immunology of Rosario and Immunology Institute, Faculty of Medical Sciences, National University of Rosario, Argentina.
Silvina R VillarIDICER-CONICET, Institute of Clinical and Experimental Immunology of Rosario and Immunology Institute, Faculty of Medical Sciences, National University of Rosario, Argentina.
Rodrigo Fernández BussyIDICER-CONICET, Institute of Clinical and Experimental Immunology of Rosario and Immunology Institute, Faculty of Medical Sciences, National University of Rosario, Argentina.
Gaëlle H MartinINSERM U955, Equipe 21, Créteil, France.
Louis PérolINSERM U932, 26 rue d'Ulm, 75005 Paris, France; Institut Curie, Section Recherche, 26 rue d'Ulm, 75005 Paris, France.
Romina ManarinIDICER-CONICET, Institute of Clinical and Experimental Immunology of Rosario and Immunology Institute, Faculty of Medical Sciences, National University of Rosario, Argentina.
Silvana V SpinelliIDICER-CONICET, Institute of Clinical and Experimental Immunology of Rosario and Immunology Institute, Faculty of Medical Sciences, National University of Rosario, Argentina.
Caroline PilonUniversité Paris-Est, UMR_S955, UPEC, Créteil, France.
José Laurent CohenINSERM U955, Equipe 21, Créteil, France; Université Paris-Est, UMR_S955, UPEC, Créteil, France; AP-HP, Hôpital Henri-Mondor - A. Chenevier, CIC-BT-504, Créteil, France.
Oscar A BottassoIDICER-CONICET, Institute of Clinical and Experimental Immunology of Rosario and Immunology Institute, Faculty of Medical Sciences, National University of Rosario, Argentina.
Eliane PiaggioINSERM U932, 26 rue d'Ulm, 75005 Paris, France; Institut Curie, Section Recherche, 26 rue d'Ulm, 75005 Paris, France; INSERM Center of Clinical Investigation (CBT507 IGR-Curie), 75005 Paris, France. Electronic address: eliane.piaggio@curie.fr.
Ana R PérezIDICER-CONICET, Institute of Clinical and Experimental Immunology of Rosario and Immunology Institute, Faculty of Medical Sciences, National University of Rosario, Argentina. Electronic address: perez_anarosa@yahoo.com.ar.
National University of Rosario · ARInstitut Curie · FRAssistance Publique – Hôpitaux de Paris · FRConsejo Nacional de Investigaciones Científicas y Técnicas · ARInserm · FRUniversité Paris-Est Créteil · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We previously showed that Trypanosomacruzi infection in C57BL/6 mice results in a lethal infection linked to unbalanced pro- and anti-inflammatory mediators production. Here, we examined the dynamics of CD4(+)Foxp3(+) regulatory T (Treg) cells within this inflammatory and highly Th1-polarized environment. Treg cells showed a reduced proliferation rate and their frequency is progressively reduced along infection compared to effector T (Teff) cells. Also, a higher fraction of Treg cells showed a naïve phenotype, meanwhile Teff cells were mostly of the effector memory type. T. cruzi infection was associated with the production of pro- and anti-inflammatory cytokines, notably IL-27p28, and with the induction of T-bet and IFN-γ expression in Treg cells. Furthermore, endogenous glucocorticoids released in response to T. cruzi-driven immune activation were crucial to sustain the Treg/Teff cell balance. Notably, IL-2 plus dexamethasone combined treatment before infection was associated with increased Treg cell proliferation and expression of GATA-3, IL-4 and IL-10, and increased mice survival time. Overall, our results indicate that therapies aimed at specifically boosting Treg cells, which during T. cruzi infection are overwhelmed by the effector immune response, represent new opportunities for the treatment of Chagas disease, which is actually only based on parasite-targeted chemotherapy.

Indexed as

AdrenalectomyAnimalsChagas CardiomyopathyChagas DiseaseCorticosteroneDexamethasoneDisease Models, AnimalGATA3 Transcription FactorGlucocorticoidsInterferon-gammaInterleukin-10Interleukin-2Interleukin-4MiceMice, Inbred C57BLMuscle, SkeletalCorticosteroneDexamethasoneGata3 protein, mouseGATA3 Transcription FactorGlucocorticoidsIL10 protein, mouseInterferon-gammaInterleukin-10Interleukin-2Interleukin-4Chagas diseaseGlucocorticoidsIFN-γIL-2Regulatory T cells

Identifiers

PMID25483139
PMCPMC7126853
OpenAlexW1993355276

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.