Evidence map›Paper›PMID 20127276›Full record

ArticleJournal of clinical immunology2010

sHLA-I Contamination, a novel mechanism to explain ex vivo/in vitro modulation of IL-10 synthesis and release in CD8(+) T lymphocytes and in neutrophils following intravenous immunoglobulin infusion.

Massimo Ghio, Paola Contini, Maurizio Setti, Gianluca Ubezio, Clemente Mazzei, Gino Tripodi

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Article in Journal of clinical immunology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-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.

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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

3 citing papers in PubMed, 9 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Massimo GhioDivision of Clinical Immunology, Department of Internal Medicine, University of Genoa Medical School, 16132, Genoa, Italy. mghio@unige.it
Paola Contini
Maurizio Setti
Gianluca Ubezio
Clemente Mazzei
Gino Tripodi
University of Genoa · ITAurelia Hospital · ITIstituto Giannina Gaslini · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNumerous mechanisms have been proposed to explain the beneficial action of intravenous immune globulin (IVIG) in autoimmune and systemic inflammatory disorders; among others, they could decrease pro-inflammatory cytokine levels and also induce anti-inflammatory cytokines. MATERIALS AND

methodsEx vivo analysis of cells from ten IVIG recipients showed significant increase of IL-10 mRNA and intra-cellular IL-10 molecules in both leukotypes.

resultsIn vitro comparable results were obtained incubating CD8(+) T lymphocytes and neutrophils from healthy donors with IVIG. sHLA-I and/or sFasL immunodepletion abolished IL-10 modulation. Co-culture with contaminant-free IgM or MabThera did not exert any mRNA modulation. Finally, IgM or MabThera plus purified sHLA-I molecules enhanced IL-10-mRNA in both leukotypes to levels comparable to those obtained with IVIG incubation.

conclusionAs IVIG infusion involves administration of soluble contaminants, these data consent to speculate that IVIG might modulate IL-10 via the immunomodulatory activities of sHLA-I contaminant molecules inducing transcriptional and post-transcriptional modulation of IL-10 in CD8(+) T lymphocytes and neutrophils.

Indexed as

ImmunotherapyCD8-Positive T-LymphocytesCells, CulturedCell SeparationDrug ContaminationFas Ligand ProteinFatigue Syndrome, ChronicFlow CytometryHistocompatibility Antigens Class IHIVHIV InfectionsHumansImmunoglobulins, IntravenousImmunologic FactorsInterleukin-10NeutrophilsFas Ligand ProteinHistocompatibility Antigens Class IImmunoglobulins, IntravenousImmunologic FactorsInterleukin-10Transforming Growth Factor beta1

Identifiers

PMID20127276
OpenAlexW1971787994

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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.