Evidence map›Paper›PMID 27586092›Full record

ArticleScientific reports2016

Enhanced immune response of MAIT cells in tuberculous pleural effusions depends on cytokine signaling.

Jing Jiang, Xinchun Chen, Hongjuan An, Bingfen Yang, Fuping Zhang, Xiaoxing Cheng

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

35 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
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  7. MAIT cells and their implication in human oral diseases.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    Review
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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 3 institutions in 1 country.

Jing JiangShenzhen Key Laboratory of Infection and Immunity, Shenzhen Third People's Hospital, Guangdong Medical College, Shenzhen, Guangdong, China.
Xinchun ChenShenzhen Key Laboratory of Infection and Immunity, Shenzhen Third People's Hospital, Guangdong Medical College, Shenzhen, Guangdong, China.
Hongjuan AnDivision of Research, Institute of Tuberculosis, 309th Hospital, Beijing, China.
Bingfen YangDivision of Research, Institute of Tuberculosis, 309th Hospital, Beijing, China.
Fuping ZhangInstitute of Microbiology, Chinese Academy of Sciences, Beijing, China.
Xiaoxing ChengDivision of Research, Institute of Tuberculosis, 309th Hospital, Beijing, China.
The 309th Hospital of Chinese People's Liberation Army · CNInstitute of Microbiology · CNShenzhen Third People’s Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The functions of MAIT cells at the site of Mycobacterium tuberculosis infection in humans are still largely unknown. In this study, the phenotypes and immune response of MAIT cells from tuberculous pleural effusions and peripheral blood were investigated. MAIT cells in tuberculous pleural effusions had greatly enhanced IFN-γ, IL-17F and granzyme B response compared with those in peripheral blood. The level of IFN-γ response in MAIT cells from tuberculous pleural effusions was inversely correlated with the extent of tuberculosis infection (p = 0.0006). To determine whether cytokines drive the immune responses of MAIT cells at the site of tuberculosis infection, the role of IL-1β, IL-2, IL-7, IL-12, IL-15 and IL-18 was investigated. Blockade of IL-2, IL-12 or IL-18 led to significantly reduced production of IFN-γ and/or granzyme B in MAIT cells from tuberculous pleural effusions. Majority of IL-2-producing cells (94.50%) in tuberculous pleural effusions had phenotype of CD3(+)CD4(+), and most IL-12p40-producing cells (91.39%) were CD14(+) cells. MAIT cells had significantly elevated expression of γc receptor which correlated with enhanced immune responses of MAIT cells. It is concluded that MAIT cells from tuberculous pleural effusions exhibited highly elevated immune response to Mtb antigens, which are controlled by cytokines produced by innate/adaptive immune cells.

Indexed as

Immunity, CellularAdultAntibodies, BlockingFemaleGene Expression RegulationGranzymesHumansInterferon-gammaInterleukin-12Interleukin-12 Subunit p40Interleukin-17Interleukin-18Interleukin-2Lipopolysaccharide ReceptorsMaleMucosal-Associated Invariant T CellsAntibodies, BlockingGranzymesIL17F protein, humanIL18 protein, humanInterferon-gammaInterleukin-12Interleukin-12 Subunit p40Interleukin-17Interleukin-18Interleukin-2Lipopolysaccharide ReceptorsReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID27586092
PMCPMC5009363
OpenAlexW2513113913

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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.