Evidence map›Paper›PMID 25233487›Full record

ArticlePLoS pathogens2014

MHC class II restricted innate-like double negative T cells contribute to optimal primary and secondary immunity to Leishmania major.

Zhirong Mou, Dong Liu, Ifeoma Okwor, Ping Jia, Kanami Orihara, Jude Ezeh Uzonna

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.5field-weighted citation impact, top 6% 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

30 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
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  16. CD3Frontiers in immunology · 2022
    Review
  17. Review
  18. Review
  19. Article
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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

6 authors at 1 institution in 1 country.

Zhirong MouDepartment of Immunology, Faculty of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
Dong LiuDepartment of Immunology, Faculty of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
Ifeoma OkworDepartment of Immunology, Faculty of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
Ping JiaDepartment of Immunology, Faculty of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
Kanami OriharaDepartment of Immunology, Faculty of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
Jude Ezeh UzonnaDepartment of Immunology, Faculty of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
University of Manitoba · CA

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

Although it is generally believed that CD4(+) T cells play important roles in anti-Leishmania immunity, some studies suggest that they may be dispensable, and that MHC II-restricted CD3(+)CD4(-)CD8(-) (double negative, DN) T cells may be more important in regulating primary anti-Leishmania immunity. In addition, while there are reports of increased numbers of DN T cells in Leishmania-infected patients, dogs and mice, concrete evidence implicating these cells in secondary anti-Leishmania immunity has not yet been documented. Here, we report that DN T cells extensively proliferate and produce effector cytokines (IFN-γ, TNF and IL-17) and granzyme B (GrzB) in the draining lymph nodes and spleens of mice following primary and secondary L. major infections. DN T cells from healed mice display functional characteristics of protective anti-Leishmania memory-like cells: rapid and extensive proliferation and effector cytokines production following L. major challenge in vitro and in vivo. DN T cells express predominantly (> 95%) alpha-beta T cell receptor (αβ TCR), are Leishmania-specific, restricted mostly by MHC class II molecules and display transcriptional profile of innate-like genes. Using in vivo depletion and adoptive transfer studies, we show that DN T cells contribute to optimal primary and secondary anti-Leishmania immunity in mice. These results directly identify DN T cells as important players in effective and protective primary and secondary anti-L. major immunity in experimental cutaneous leishmaniasis.

Indexed as

Adoptive TransferAnimalsBlotting, WesternCells, CulturedCytokinesFemaleHistocompatibility Antigens Class IIImmunity, InnateImmunoenzyme TechniquesLeishmania majorLeishmaniasis, CutaneousMiceMice, Inbred C57BLReal-Time Polymerase Chain ReactionReceptors, Antigen, T-Cell, alpha-betaReverse Transcriptase Polymerase Chain ReactionCytokinesHistocompatibility Antigens Class IIReceptors, Antigen, T-Cell, alpha-betaRNA, Messenger

Identifiers

PMID25233487
PMCPMC4169504
OpenAlexW2062213647

What OpenQuestion holds

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LicenceCC BY
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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.