Autoantibodies in Rheumatoid Arthritis: Historical Background and Novel Findings.


Journal

Clinical reviews in allergy & immunology
ISSN: 1559-0267
Titre abrégé: Clin Rev Allergy Immunol
Pays: United States
ID NLM: 9504368

Informations de publication

Date de publication:
Oct 2022
Historique:
accepted: 24 08 2021
pubmed: 9 9 2021
medline: 14 9 2022
entrez: 8 9 2021
Statut: ppublish

Résumé

Autoantibodies represent a hallmark of rheumatoid arthritis (RA), with the rheumatoid factor (RF) and antibodies against citrullinated proteins (ACPA) being the most acknowledged ones. RA patients who are positive for RF and/or ACPA ("seropositive") in general display a different etiology and disease course compared to so-called "seronegative" patients. Still, the seronegative patient population is very heterogeneous and not well characterized. Due to the identification of new autoantibodies and advancements in the diagnosis of rheumatic diseases in the last years, the group of seronegative patients is constantly shrinking. Aside from antibodies towards various post-translational modifications, recent studies describe autoantibodies targeting some native proteins, further broadening the spectrum of recognized antigens. Next to the detection of new autoantibody groups, much research has been done to answer the question if and how autoantibodies contribute to the pathogenesis of RA. Since autoantibodies can be detected years prior to RA onset, it is a matter of debate whether their presence alone is sufficient to trigger the disease. Nevertheless, there is gathering evidence of direct autoantibody effector functions, such as stimulation of osteoclastogenesis and synovial fibroblast migration in in vitro experiments. In addition, autoantibody positive patients display a worse clinical course and stronger radiographic progression. In this review, we discuss current findings regarding different autoantibody types, the underlying disease-driving mechanisms, the role of Fab and Fc glycosylation and clinical implications.

Identifiants

pubmed: 34495490
doi: 10.1007/s12016-021-08890-1
pii: 10.1007/s12016-021-08890-1
pmc: PMC9464122
doi:

Substances chimiques

Autoantibodies 0
Rheumatoid Factor 9009-79-4

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

138-151

Subventions

Organisme : deutsche forschungsgemeinschaft
ID : FOR2886 PANDORA
Organisme : deutsche forschungsgemeinschaft
ID : SPP1468-IMMUNOBONE
Organisme : innovative medicines initiative
ID : RTCure grant (no. 777357)
Organisme : bundesministerium für bildung und forschung
ID : MASCARA

Informations de copyright

© 2021. The Author(s).

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Auteurs

Maria V Sokolova (MV)

Department of Internal Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-Universität Erlangen-Nürnberg and Universitätsklinikum Erlangen, Universitätstrasse 25a, 91054, Erlangen, Germany.
Deutsches Zentrum Für Immuntherapie, Friedrich-Alexander-Universität Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.

Georg Schett (G)

Department of Internal Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-Universität Erlangen-Nürnberg and Universitätsklinikum Erlangen, Universitätstrasse 25a, 91054, Erlangen, Germany.
Deutsches Zentrum Für Immuntherapie, Friedrich-Alexander-Universität Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.

Ulrike Steffen (U)

Department of Internal Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-Universität Erlangen-Nürnberg and Universitätsklinikum Erlangen, Universitätstrasse 25a, 91054, Erlangen, Germany. ulrike.steffen@uk-erlangen.de.
Deutsches Zentrum Für Immuntherapie, Friedrich-Alexander-Universität Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany. ulrike.steffen@uk-erlangen.de.

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