Evidence map›Paper›PMID 33810246›Full record

ReviewInternational journal of molecular sciences2021

Hyposialylation Must Be Considered to Develop Future Therapies in Autoimmune Diseases.

Anne Bordron, Marie Morel, Cristina Bagacean, Maryvonne Dueymes, Pierre Pochard, Anne Harduin-Lepers, Christophe Jamin, Jacques-Olivier Pers

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. 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
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

14 citing papers in PubMed, 21 citations in OpenAlex.

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  14. Identification of Metabolism-Associated Molecular Subtypes of Chronic Obstructive Pulmonary Disease.International journal of chronic obstructive pulmonary disease · 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 3 institutions in 1 country.

Anne BordronUniv Brest, Inserm, LBAI, UMR1227 Brest, France.ORCID 0000-0002-7886-2546
Marie MorelUniv Brest, Inserm, LBAI, UMR1227 Brest, France.
Cristina BagaceanUniv Brest, Inserm, LBAI, UMR1227 Brest, France.
Maryvonne DueymesUniv Brest, Inserm, LBAI, UMR1227 Brest, France.
Pierre PochardCHU de Brest, Laboratory of Immunolgy, 29200 Brest, France.
Anne Harduin-LepersUniv. Lille, CNRS UMR 8576-UGSF-Unité de Glycobiologie Structurale et Fonctionnelle, 59000 Lille, France.ORCID 0000-0002-1233-3799
Christophe JaminUniv Brest, Inserm, LBAI, UMR1227 Brest, France.ORCID 0000-0002-9494-3223
Jacques-Olivier PersUniv Brest, Inserm, LBAI, UMR1227 Brest, France.ORCID 0000-0001-7287-5541
Inserm · FRCentre Hospitalier Régional Universitaire de Brest · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoimmune disease development depends on multiple factors, including genetic and environmental. Abnormalities such as sialylation levels and/or quality have been recently highlighted. The adjunction of sialic acid at the terminal end of glycoproteins and glycolipids is essential for distinguishing between self and non-self-antigens and the control of pro- or anti-inflammatory immune reactions. In autoimmunity, hyposialylation is responsible for chronic inflammation, the anarchic activation of the immune system and organ lesions. A detailed characterization of this mechanism is a key element for improving the understanding of these diseases and the development of innovative therapies. This review focuses on the impact of sialylation in autoimmunity in order to determine future treatments based on the regulation of hyposialylation.

Indexed as

Protein Processing, Post-TranslationalAnimalsAutoantibodiesAutoimmune DiseasesHumansImmunophenotypingPrecision MedicineSialic AcidsAutoantibodiesSialic Acidsautoimmune diseasesCD22immunoglobulinsialic acidsialyltransferasetherapies

Identifiers

PMID33810246
PMCPMC8036829
OpenAlexW3151112158

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.