Evidence map›Paper›PMID 24682714›Full record

ArticleJournal of clinical immunology2014

Natural autoantibodies to Fcγ receptors in intravenous immunoglobulins.

Hicham Bouhlal, Denis Martinvalet, Jean-Luc Teillaud, Catherine Fridman, Michel D Kazatchkine, Jagadeesh Bayry, Sébastien Lacroix-Desmazes, Srini V Kaveri

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Article in Journal of clinical immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

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  6. Recombinant Proteins and Monoclonal Antibodies.Advances in biochemical engineering/biotechnology · 2021
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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

8 authors at 6 institutions in 3 countries.

Hicham BouhlalEA 4666 UFR de Médecine, CAP-Santé (FED 4231), Université de Picardie Jules Verne UPJV, Amiens, France.
Denis Martinvalet
Jean-Luc Teillaud
Catherine Fridman
Michel D Kazatchkine
Jagadeesh Bayry
Sébastien Lacroix-Desmazes
Srini V Kaveri
Inserm · FRDélégation Paris 5 · FRIndian Council of Medical Research · INJoint United Nations Programme on HIV/AIDS · CHSorbonne Université · FRUniversité de Picardie Jules Verne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A considerable progress has been achieved in the comprehension of the cellular and molecular mechanisms that account for the therapeutic benefit of intravenous immunoglobulin (IVIg) in several autoimmune and inflammatory conditions. However, the precise mechanisms responsible for such a wide range of biological activities have not been proven unambiguously. A wide range of specificities have been identified within IVIg including idiotypes of immunoglobulins, T cell receptor, HLA molecules, several cell surface molecules of immunological importance such as CD4, CD5, Fas, BAFF, cytokines and cytokine receptors, chemokine receptors, CD40 among others. Here we identify and characterize the natural autoantibodies of IgG isotype directed against the human Fc receptors. We show that the F(ab')2 of IVIg recognize the FcγRIII (CD16) and FcγRII (CD32). Interestingly, the immunopurified anti-FcγIII and anti-FcγII antibodies isolated from IVIg bind soluble and membrane-bound FcR and inhibit rosette formation. Altogether, these results along with previous reports provide pointers on the existence of functionally relevant natural autoantibodies towards a wide range of self-motifs that may participate in regulation of the immune response. Their presence in the therapeutic immunoglobulin preparations may explain at least in part, the beneficial effect of IVIg in autoimmune diseases.

Indexed as

AutoantibodiesAutoimmune DiseasesChromatography, AffinityCytokinesHumansImmunity, InnateImmunoglobulin GImmunoglobulins, IntravenousImmunotherapyJurkat CellsReceptors, IgGAutoantibodiesCytokinesImmunoglobulin GImmunoglobulins, IntravenousReceptors, IgG

Identifiers

PMID24682714
OpenAlexW2078998661

What OpenQuestion holds

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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.