Evidence map›Paper›PMID 29103189›Full record

ArticleJournal of clinical immunology2018

Modulation of the Interleukin-21 Pathway with Interleukin-4 Distinguishes Common Variable Immunodeficiency Patients with More Non-infectious Clinical Complications.

Marylin Desjardins, Marianne Béland, Marieme Dembele, Duncan Lejtenyi, Jean-Phillipe Drolet, Martine Lemire, Christos Tsoukas, Moshe Ben-Shoshan, Francisco J D Noya, Reza Alizadehfar and 2 more

Abstract read
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In one paragraph

Article in Journal of clinical immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
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  5. Review
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  10. A Unique HeterozygousFrontiers in immunology · 2018
    Article
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 2 institutions in 1 country.

Marylin DesjardinsDivision of Allergy and Immunology, Department of Paediatrics, McGill University Health Centre, Montreal, Quebec, Canada. marylin.desjardins@mcgill.ca.ORCID 0000-0001-7914-8398
Marianne BélandMeakins-Christie Laboratories of the Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada.
Marieme DembeleMeakins-Christie Laboratories of the Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada.
Duncan LejtenyiDivision of Allergy and Immunology, Department of Paediatrics, McGill University Health Centre, Montreal, Quebec, Canada.
Jean-Phillipe DroletDivision of Allergy and Clinical Immunology, Department of Medicine, Centre Hospitalier Universitaire de Quebec, Quebec City, Quebec, Canada.
Martine LemireDivision of Allergy & Clinical Immunology, Department of Medicine, McGill University Health Centre, Montreal, Quebec, Canada.
Christos TsoukasDivision of Allergy & Clinical Immunology, Department of Medicine, McGill University Health Centre, Montreal, Quebec, Canada.
Moshe Ben-ShoshanDivision of Allergy and Immunology, Department of Paediatrics, McGill University Health Centre, Montreal, Quebec, Canada.
Francisco J D NoyaDivision of Allergy and Immunology, Department of Paediatrics, McGill University Health Centre, Montreal, Quebec, Canada.
Reza AlizadehfarDivision of Allergy and Immunology, Department of Paediatrics, McGill University Health Centre, Montreal, Quebec, Canada.
Christine T McCuskerDivision of Allergy and Immunology, Department of Paediatrics, McGill University Health Centre, Montreal, Quebec, Canada.
Bruce D MazerDivision of Allergy and Immunology, Department of Paediatrics, McGill University Health Centre, Montreal, Quebec, Canada.
McGill University Health Centre · CACentre hospitalier universitaire de Québec · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCommon variable immunodeficiency (CVID) is characterized by hypogammaglobulinemia and clinical manifestations such as infections, autoimmunity, and malignancy. We sought to determine if responsiveness to interleukin-21 (IL-21), a key cytokine for B cell differentiation, correlates with distinct clinical phenotypes in CVID.

methodsCVID subjects were recruited through the Canadian Primary Immunodeficiency Evaluative Survey registry. Peripheral blood mononuclear cells were cultured with anti-CD40 ± interferon-gamma, interleukin-4 (IL-4), IL-21, and/or IL-4+IL-21. B cell subpopulations and IgG production were determined at baseline and day 7 by flow cytometry and ELISA. Clinical complications were compared using contingency tables.

resultsCVID subjects exhibited decreased CD27

conclusionsThe IL-4 and IL-21 in vitro assays distinguish two groups of CVID subjects and can be used with baseline B cell subpopulation phenotyping to better identify patients experiencing more vs. fewer clinical non-infectious complications and potentially to modulate therapy.

Indexed as

AdultB-LymphocytesB-Lymphocyte SubsetsCells, CulturedCommon Variable ImmunodeficiencyDiagnosis, DifferentialFemaleHumansImmunoglobulin GImmunologic MemoryImmunophenotypingInterleukin-21Interleukin-4InterleukinsLymphocyte ActivationMaleImmunoglobulin GInterleukin-21Interleukin-4InterleukinsTumor Necrosis Factor Receptor Superfamily, Member 7antibody productionB lymphocytesCommon Variable Immunodeficiencyhumoral immune responseinterleukin-21interleukin-4

Identifiers

PMID29103189
OpenAlexW2765268617

What OpenQuestion holds

Textmetadata
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.