Evidence map›Paper›PMID 26553468›Full record

ArticleInfection and immunity2016

Suppression of CD4+ Effector Responses by Naturally Occurring CD4+ CD25+ Foxp3+ Regulatory T Cells Contributes to Experimental Cerebral Malaria.

Anne-Laurence Blanc, Tarun Keswani, Olivier Gorgette, Antonio Bandeira, Bernard Malissen, Pierre-André Cazenave, Sylviane Pied

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 92% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. The IL-33/ST2 Pathway in Cerebral Malaria.International journal of molecular sciences · 2022
    Review
  2. 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

7 authors at 2 institutions in 1 country.

Anne-Laurence BlancDépartement d'Immunologie, Institut Pasteur, Paris, France Université Pierre et Marie Curie, Paris, France Univ. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR 8204-CIIL-Centre d'Infection et d'Immunité de Lille, Lille, France.
Tarun KeswaniUniv. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR 8204-CIIL-Centre d'Infection et d'Immunité de Lille, Lille, France.
Olivier GorgetteUnité d'Immunologie Moléculaire des Parasites, Institut Pasteur, Paris, France.
Antonio BandeiraDépartement d'Immunologie, Institut Pasteur, Paris, France Unité de Biologie des Populations Lymphocytaires, Institut Pasteur, Paris, France.
Bernard MalissenINSERM U 631-CNRS UMR 6102, Université de la Méditerranée, Centre d'Immunologie de Marseille-Luminy, Marseille, France.
Pierre-André CazenaveDépartement d'Immunologie, Institut Pasteur, Paris, France Université Pierre et Marie Curie, Paris, France CNRS UMR 7211, Université Pierre et Marie Curie, Hôpital de la Pitié-Salpêtrière, Paris, France Univ. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR 8204-CIIL-Centre d'Infection et d'Immunité de Lille, Lille, France.
Sylviane PiedDépartement d'Immunologie, Institut Pasteur, Paris, France Univ. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR 8204-CIIL-Centre d'Infection et d'Immunité de Lille, Lille, France sylviane.pied@pasteur-lille.fr.ORCID http://orcid.org/0000-0003-0642-1423
Centre National de la Recherche Scientifique · FRInstitut Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of naturally occurring CD4(+) CD25(+) Foxp3(+) regulatory T cells (nTreg) in the pathogenesis of cerebral malaria (CM), which involves both pathogenic T cell responses and parasite sequestration in the brain, is still unclear. To assess the contribution and dynamics of nTreg during the neuropathogenesis, we unbalanced the ratio between nTreg and naive CD4(+) T cells in an attenuated model of Plasmodium berghei ANKA-induced experimental CM (ECM) by using a selective cell enrichment strategy. We found that nTreg adoptive transfer accelerated the onset and increased the severity of CM in syngeneic C57BL/6 (B6) P. berghei ANKA-infected mice without affecting the level of parasitemia. In contrast, naive CD4(+) T cell enrichment prevented CM and promoted parasite clearance. Furthermore, early during the infection nTreg expanded in the spleen but did not efficiently migrate to the site of neuroinflammation, suggesting that nTreg exert their pathogenic action early in the spleen by suppressing the protective naive CD4(+) T cell response to P. berghei ANKA infection in vivo in both CM-susceptible (B6) and CM-resistant (B6-CD4(-/-)) mice. However, their sole transfer was not sufficient to restore CM susceptibility in two CM-resistant congenic strains tested. Altogether, these results demonstrate that nTreg are activated and functional during P. berghei ANKA infection and that they contribute to the pathogenesis of CM. They further suggest that nTreg may represent an early target for the modulation of the immune response to malaria.

Indexed as

Adoptive TransferAnimalsBrainCD4 AntigensCell MovementForkhead Transcription FactorsInterleukin-2 Receptor alpha SubunitMalaria, CerebralMiceMice, Inbred C57BLMice, KnockoutPlasmodium bergheiSpleenT-Lymphocytes, RegulatoryCD4 AntigensForkhead Transcription FactorsFoxp3 protein, mouseInterleukin-2 Receptor alpha Subunit

Identifiers

PMID26553468
PMCPMC4694001
OpenAlexW2100377598

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.