Evidence map›Paper›PMID 23646169›Full record

ArticlePloS one2013

Angiotensin II is a new component involved in splenic T lymphocyte responses during Plasmodium berghei ANKA infection.

João Luiz Silva-Filho, Mariana Conceição Souza, Claudio Teixeira Ferreira-Dasilva, Leandro Souza Silva, Maria Fernanda Souza Costa, Tatiana Almeida Padua, Maria das Graças Henriques, Alexandre Morrot, Wilson Savino, Celso Caruso-Neves and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.6field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. CD8Frontiers in cellular and infection microbiology · 2025
    Article
  4. Review
  5. Article
  6. Article
  7. Is there a role for bradykinin in cerebral malaria pathogenesis?Frontiers in cellular and infection microbiology · 2023
    Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Kinins Released by Erythrocytic Stages ofFrontiers in medicine · 2019
    Article
  16. Article
  17. Article
  18. Targeting Angiotensin II Type-1 Receptor (ATFrontiers in cellular and infection microbiology · 2017
    Article
  19. Review
  20. Angiotensin II type-1 receptor (ATScientific reports · 2016
    Article
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

11 authors at 2 institutions in 1 country.

João Luiz Silva-FilhoInstituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Mariana Conceição Souza
Claudio Teixeira Ferreira-Dasilva
Leandro Souza Silva
Maria Fernanda Souza Costa
Tatiana Almeida Padua
Maria das Graças Henriques
Alexandre Morrot
Wilson Savino
Celso Caruso-Neves
Ana Acacia Sá Pinheiro
Universidade Federal do Rio de Janeiro · BRFundação Oswaldo Cruz · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The contribution of T cells in severe malaria pathogenesis has been described. Here, we provide evidence for the potential role of angiotensin II (Ang II) in modulating splenic T cell responses in a rodent model of cerebral malaria. T cell activation induced by infection, determined by 3 to 4-fold enhancement in CD69 expression, was reduced to control levels when mice were treated with 20 mg/kg losartan (IC₅₀ = 0.966 mg/kg/d), an AT₁ receptor antagonist, or captopril (IC₅₀ = 1.940 mg/kg/d), an inhibitor of angiotensin-converting enzyme (ACE). Moreover, the production of interferon-γ and interleukin-17 by CD4+ T cells diminished 67% and 70%, respectively, by both treatments. Losartan reduced perforin expression in CD8+ T cells by 33% while captopril completely blocked it. The upregulation in chemokine receptor expression (CCR2 and CCR5) observed during infection was abolished and CD11a expression was partially reduced when mice were treated with drugs. T cells activated by Plasmodium berghei ANKA antigens showed 6-fold enhance in AT₁ levels in comparison with naive cells. The upregulation of AT₁ expression was reduced by losartan (80%) but not by captopril. Our results suggest that the AT₁/Ang II axis has a role in the establishment of an efficient T cell response in the spleen and therefore could participate in a misbalanced parasite-induced T cell immune response during P. berghei ANKA infection.

Indexed as

Angiotensin IIAngiotensin II Type 1 Receptor BlockersAnimalsCell AdhesionCell LineCell MovementCytokinesDisease Models, AnimalInflammation MediatorsLymphocyte ActivationMalariaMalaria, CerebralMicePlasmodium bergheiSpleenT-Lymphocyte SubsetsAngiotensin IIAngiotensin II Type 1 Receptor BlockersCytokinesInflammation Mediators

Identifiers

PMID23646169
PMCPMC3639972
OpenAlexW2034880823

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.