Evidence map›Paper›PMID 34093549›Full record

ArticleFrontiers in immunology2021

High Dose Intravenous IgG Therapy Modulates Multiple NK Cell and T Cell Functions in Patients With Immune Dysregulation.

Sarah M McAlpine, Sarah E Roberts, John J Heath, Fabian Käsermann, Andrew C Issekutz, Thomas B Issekutz, Beata Derfalvi

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

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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

7 authors at 2 institutions in 2 countries.

Sarah M McAlpineDepartment of Pediatrics, Dalhousie University, Halifax, NS, Canada.
Sarah E RobertsDepartment of Pediatrics, Dalhousie University, Halifax, NS, Canada.
John J HeathDepartment of Pediatrics, Dalhousie University, Halifax, NS, Canada.
Fabian KäsermannCSL Behring Research, CSL Biologics Research Center, Bern, Switzerland.
Andrew C IssekutzDepartment of Pediatrics, Dalhousie University, Halifax, NS, Canada.
Thomas B IssekutzDepartment of Pediatrics, Dalhousie University, Halifax, NS, Canada.
Beata DerfalviDepartment of Pediatrics, Dalhousie University, Halifax, NS, Canada.
Dalhousie University · CACSL (Switzerland) · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intravenous immunoglobulin (IVIG) is an effective immunomodulatory treatment for immune dysregulation diseases. However, the mechanisms by which it reduces systemic inflammation are not well understood. NK cell cytotoxicity is decreased by IVIG in women with reduced fertility, but IVIG effects on NK cells in immune dysregulation are less clear. We hypothesized that IVIG modulation of lymphocyte function, especially in NK cells, is important for resolution of inflammation. Our aim was to identify IVIG-induced changes in a cohort of patients with Kawasaki disease (KD) and those that occur broadly in pediatric patients with various immune dysregulatory diseases. Peripheral blood mononuclear cells (PBMCs) of patients with KD or autoimmune/inflammatory diseases were phenotyped pre and post high dose IVIG treatment by flow cytometry. In KD patients, after IVIG infusion T

Indexed as

AdolescentCD4-Positive T-LymphocytesChildChild, PreschoolCohort StudiesFemaleFlow CytometryHumansImmunoglobulins, IntravenousImmunomodulationInflammationKiller Cells, NaturalLeukocytes, MononuclearMaleMucocutaneous Lymph Node SyndromeT-Lymphocytes, RegulatoryImmunoglobulins, Intravenousautoimmune diseaseimmune dysregulationIVIGKawasaki diseaseNK cell

Identifiers

PMID34093549
PMCPMC8170153
OpenAlexW3163080462

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.