Evidence map›Paper›PMID 34238985›Full record

ArticleScientific reports2021

In vitro Interleukin-7 treatment partially rescues MAIT cell dysfunction caused by SARS-CoV-2 infection.

Satanay Hubrack, Maryam Ali Al-Nesf, Nourhen Agrebi, Christophe Raynaud, Mohammed Abu Khattab, Merlin Thomas, Tayseer Ibrahim, Salma Taha, Said Dermime, Maysaloun Merhi and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

13 citing papers in PubMed, 14 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. The Emerging Role of MAIT Cell Responses in Viral Infections.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Review
  9. Review
  10. Review
  11. Review
  12. Frontiers in immunology · 2022
    Article
  13. 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

14 authors at 5 institutions in 3 countries.

Satanay Hubrack *Department of Human Genetics, Research Branch, Sidra Medicine, 26999, Doha, Qatar. Shubrack@sidra.org.ORCID 0000-0003-1095-7386
Maryam Ali Al-Nesf *Allergy and Clinical Immunology Section, Hamad Medical Corporation, 3050, Doha, Qatar.
Nourhen AgrebiDepartment of Human Genetics, Research Branch, Sidra Medicine, 26999, Doha, Qatar.
Christophe RaynaudDepartment of Human Genetics, Research Branch, Sidra Medicine, 26999, Doha, Qatar.
Mohammed Abu KhattabDivision of Infectious Disease, Hamad Medical Corporation, 3050, Doha, Qatar.
Merlin ThomasPulmonary Division, Hamad Medical Corporation, 3050, Doha, Qatar.
Tayseer IbrahimAllergy and Clinical Immunology Section, Hamad Medical Corporation, 3050, Doha, Qatar.
Salma TahaAllergy and Clinical Immunology Section, Hamad Medical Corporation, 3050, Doha, Qatar.
Said DermimeTranslational Cancer Research Facility, National Center for Cancer Care and Research, Translational Research Institute, Hamad Medical Corporation, 3050, Doha, Qatar.ORCID 0000-0002-5526-7496
Maysaloun MerhiTranslational Cancer Research Facility, National Center for Cancer Care and Research, Translational Research Institute, Hamad Medical Corporation, 3050, Doha, Qatar.
Michal KulinskiTranslational Research Institute, Hamad Medical Corporation, 3050, Doha, Qatar.
Martin SteinhoffTranslational Research Institute, Hamad Medical Corporation, 3050, Doha, Qatar.
Patrick TangDepartment of Pathology, Sidra Medicine, 26999, Doha, Qatar.ORCID 0000-0003-1583-5484
Bernice LoDepartment of Human Genetics, Research Branch, Sidra Medicine, 26999, Doha, Qatar. blo@sidra.org.
Hamad Medical Corporation · QAQatar Airways (Qatar) · QANational Center for Cancer Care and Research · QACornell University · USThe Royal Free Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MAIT cells have been shown to be activated upon several viral infections in a TCR-independent manner by responding to inflammatory cytokines secreted by antigen-presenting cells. Recently, a few studies have shown a similar activation of MAIT cells in response to severe acute respiratory coronavirus 2 (SARS-CoV-2) infection. In this study, we investigate the effect of SARS-CoV-2 infection on the frequency and phenotype of MAIT cells by flow cytometry, and we test in vitro stimulation conditions on the capacity to enhance or rescue the antiviral function of MAIT cells from patients with coronavirus disease 2019 (COVID-19). Our study, in agreement with recently published studies, confirmed the decline in MAIT cell frequency of hospitalized donors in comparison to healthy donors. MAIT cells of COVID-19 patients also had lower expression levels of TNF-alpha, perforin and granzyme B upon stimulation with IL-12 + IL-18. 24 h' incubation with IL-7 successfully restored perforin expression levels in COVID-19 patients. Combined, our findings support the growing evidence that SARS-CoV-2 is dysregulating MAIT cells and that IL-7 treatment might improve their function, rendering them more effective in protecting the body against the virus.

Indexed as

Cells, CulturedCOVID-19FemaleGranzymesHumansInterleukin-7MaleMucosal-Associated Invariant T CellsPerforinSARS-CoV-2Tumor Necrosis Factor-alphaGranzymesInterleukin-7PerforinTumor Necrosis Factor-alpha

Identifiers

PMID34238985
PMCPMC8266862
OpenAlexW3178922432

What OpenQuestion holds

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LicenceCC BY
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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.