Evidence map›Paper›PMID 31681293›Full record

Trial reportFrontiers in immunology2019

Adaptive Features of Natural Killer Cells in Multiple Sclerosis.

Antía Moreira, Elisenda Alari-Pahissa, Elvira Munteis, Andrea Vera, Ana Zabalza, Mireia Llop, Noelia Villarrubia, Marcel Costa-García, Roberto Álvarez-Lafuente, Luisa María Villar and 2 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. Natural Killer Cells: Dual Regulators and Therapeutic Targets in Multiple Sclerosis Immunopathogenesis.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2026
    Review
  2. Review
  3. Article
  4. Review
  5. Natural killer cells in multiple sclerosis: foe or friends?Frontiers in cellular neuroscience · 2025
    Review
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  7. Review
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  9. Observational
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  11. Review
  12. Article
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  16. 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

12 authors at 6 institutions in 1 country.

Antía MoreiraNeurology Department, Hospital del Mar Medical Research Institute (IMIM), Barcelona, Spain.
Elisenda Alari-PahissaUniversity Pompeu Fabra, Barcelona, Spain.
Elvira MunteisNeurology Department, Hospital del Mar Medical Research Institute (IMIM), Barcelona, Spain.
Andrea VeraNeurology Department, Hospital del Mar Medical Research Institute (IMIM), Barcelona, Spain.
Ana ZabalzaNeurology Department, Hospital del Mar Medical Research Institute (IMIM), Barcelona, Spain.
Mireia LlopNeurology Department, Hospital del Mar Medical Research Institute (IMIM), Barcelona, Spain.
Noelia VillarrubiaImmunology Department, Hospital Universitario Ramón y Cajal, Madrid, Spain.
Marcel Costa-GarcíaUniversity Pompeu Fabra, Barcelona, Spain.
Roberto Álvarez-LafuenteNeurology Service, Instituto de Investigación Sanitaria del Hospital Clínico de San Carlos, Madrid, Spain.
Luisa María VillarImmunology Department, Hospital Universitario Ramón y Cajal, Madrid, Spain.
Miguel López-BotetUniversity Pompeu Fabra, Barcelona, Spain.
Jose E Martínez-RodríguezNeurology Department, Hospital del Mar Medical Research Institute (IMIM), Barcelona, Spain.
Hospital del Mar Research Institute · ESPompeu Fabra University · ESHospital Del Mar · ESHospital Universitario Ramón y Cajal · ESAlthaia · ESInstituto de Investigación Sanitaria del Hospital Clínico San Carlos · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human cytomegalovirus (HCMV) has been recently related with a lower susceptibility to multiple sclerosis (MS). HCMV promotes an adaptive development of NK cells bearing the CD94/NKG2C receptor with a characteristic phenotypic and functional profile. NK cells are proposed to play an immunoregulatory role in MS, and expansion of the NKG2C(+) subset was recently associated with reduced disability progression. To further explore this issue, additional adaptive NK cell markers, i.e., downregulation of FcεRIγ chain (FcRγ) and PLZF transcription factor, as well as antibody-dependent NK cell activation were assessed in controls and MS patients considering HCMV serology and clinical features. In line with previous reports, increased proportions of NKG2C(+), FcRγ(-), and PLZF(-) CD56

Indexed as

Lymphocyte ActivationAdultCytomegalovirusFemaleHumansKiller Cells, NaturalMaleMiddle AgedMultiple SclerosisNK Cell Lectin-Like Receptor Subfamily CNK Cell Lectin-Like Receptor Subfamily DPromyelocytic Leukemia Zinc Finger ProteinProspective StudiesReceptors, FcTumor Necrosis Factor-alphaFCER1G, humanKLRC2 protein, humanKLRD1 protein, humanNK Cell Lectin-Like Receptor Subfamily CNK Cell Lectin-Like Receptor Subfamily DPromyelocytic Leukemia Zinc Finger ProteinReceptors, FcTumor Necrosis Factor-alphaZBTB16 protein, humancytomegalovirusFcεRIγmultiple sclerosisnatural killer cellsNKG2CPLZF

Identifiers

PMID31681293
PMCPMC6803486
OpenAlexW2980682853

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.