Evidence map›Paper›PMID 29515123›Full record

Trial reportScientific reports2018

Enumeration, functional responses and cytotoxic capacity of MAIT cells in newly diagnosed and relapsed multiple myeloma.

Nicholas A Gherardin, Liyen Loh, Lorenztino Admojo, Alexander J Davenport, Kelden Richardson, Amy Rogers, Phillip K Darcy, Misty R Jenkins, H Miles Prince, Simon J Harrison and 8 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed, 1 pooled it
8.5field-weighted citation impact, top 2% 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

65 citing papers in PubMed, 1 synthesis or guideline pooled it, 100 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. T Cells Dysfunction in Multiple Myeloma.ImmunoTargets and therapy · 2025
    Review
  14. Review
  15. MAIT Cells in the Bone Marrow of Patients with Aplastic Anemia.International journal of molecular sciences · 2024
    Article
  16. High pre-transplant Mucosal Associated Invariant T Cell (MAIT) count predicts favorable course of myeloid aplasia.Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia · 2024
    Article
  17. Article
  18. Article
  19. Review
  20. Article

5 more citing papers are in PubMed but not listed here.

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

18 authors at 3 institutions in 1 country.

Nicholas A GherardinDepartment of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, Victoria, 3010, Australia.
Liyen LohDepartment of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, Victoria, 3010, Australia.
Lorenztino AdmojoCancer Immunology Program, Peter MacCallum Cancer Centre, Melbourne, Victoria, 3000, Australia.ORCID 0000-0002-3674-6205
Alexander J DavenportCancer Immunology Program, Peter MacCallum Cancer Centre, Melbourne, Victoria, 3000, Australia.
Kelden RichardsonCancer Immunology Program, Peter MacCallum Cancer Centre, Melbourne, Victoria, 3000, Australia.
Amy RogersCancer Immunology Program, Peter MacCallum Cancer Centre, Melbourne, Victoria, 3000, Australia.ORCID 0000-0002-1696-4299
Phillip K DarcyCancer Immunology Program, Peter MacCallum Cancer Centre, Melbourne, Victoria, 3000, Australia.
Misty R JenkinsCancer Immunology Program, Peter MacCallum Cancer Centre, Melbourne, Victoria, 3000, Australia.
H Miles PrinceCancer Immunology Program, Peter MacCallum Cancer Centre, Melbourne, Victoria, 3000, Australia.
Simon J HarrisonCancer Immunology Program, Peter MacCallum Cancer Centre, Melbourne, Victoria, 3000, Australia.
Hang QuachCancer Immunology Program, Peter MacCallum Cancer Centre, Melbourne, Victoria, 3000, Australia.
David P FairlieDivision of Chemistry & Structural Biology, Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland, 4072, Australia.
Katherine KedzierskaDepartment of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, Victoria, 3010, Australia.
James McCluskeyDepartment of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, Victoria, 3010, Australia.ORCID 0000-0002-8597-815X
Adam P UldrichDepartment of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, Victoria, 3010, Australia.
Paul J NeesonCancer Immunology Program, Peter MacCallum Cancer Centre, Melbourne, Victoria, 3000, Australia.
David S RitchieCancer Immunology Program, Peter MacCallum Cancer Centre, Melbourne, Victoria, 3000, Australia.
Dale I GodfreyDepartment of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, Victoria, 3010, Australia. godfrey@unimelb.edu.au.ORCID 0000-0002-3009-5472
The University of Melbourne · AUThe Royal Melbourne Hospital · AUThe University of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mucosal-associated invariant T (MAIT) cells are T cells that recognise vitamin-B derivative Ag presented by the MHC-related-protein 1 (MR1) antigen-presenting molecule. While MAIT cells are highly abundant in humans, their role in tumour immunity remains unknown. Here we have analysed the frequency and function of MAIT cells in multiple myeloma (MM) patients. We show that MAIT cell frequency in blood is reduced compared to healthy adult donors, but comparable to elderly healthy control donors. Furthermore, there was no evidence that MAIT cells accumulated at the disease site (bone marrow) of these patients. Newly diagnosed MM patient MAIT cells had reduced IFNγ production and CD27 expression, suggesting an exhausted phenotype, although IFNγ-producing capacity is restored in relapsed/refractory patient samples. Moreover, immunomodulatory drugs Lenalidomide and Pomalidomide, indirectly inhibited MAIT cell activation. We further show that cell lines can be pulsed with vitamin-B derivative Ags and that these can be presented via MR1 to MAIT cells in vitro, to induce cytotoxic activity comparable to that of natural killer (NK) cells. Thus, MAIT cells are reduced in MM patients, which may contribute to disease in these individuals, and moreover, MAIT cells may represent new immunotherapeutic targets for treatment of MM and other malignancies.

Indexed as

Immunity, CellularFemaleHumansInterferon-gammaKiller Cells, NaturalLenalidomideMaleMucosal-Associated Invariant T CellsMultiple MyelomaNeoplasm ProteinsThalidomideTumor Necrosis Factor Receptor Superfamily, Member 7IFNG protein, humanInterferon-gammaLenalidomideNeoplasm ProteinspomalidomideThalidomideTumor Necrosis Factor Receptor Superfamily, Member 7

Identifiers

PMID29515123
PMCPMC5841305
OpenAlexW2794278101

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.