Clinical and biological activity of rituximab in the treatment of pemphigus.

B-cell depletion therapy CD20 monoclonal antibody pemphigus rituximab

Journal

Immunotherapy
ISSN: 1750-7448
Titre abrégé: Immunotherapy
Pays: England
ID NLM: 101485158

Informations de publication

Date de publication:
01 2021
Historique:
pubmed: 14 10 2020
medline: 19 1 2022
entrez: 13 10 2020
Statut: ppublish

Résumé

B-cells are major effector cells in autoimmunity since they differentiate into plasmocytes that produce pathogenic auto-antibody such as anti-desmoglein antibodies in pemphigus patients. Major advances were obtained using whole B-cell depleting therapies including anti-CD20 antibodies in refractory pemphigus patients that lead to rituximab approval in pemphigus patients in EU and USA. This review summarizes the data supporting the efficacy of rituximab in pemphigus and provides an overview of the reported immunological changes underlying its therapeutic action. Short and long-term remission in pemphigus is explained by the removal of autoreactive B-cells involved in the production of pathogenic IgG auto-antibodies and by enhancement of the appearance of regulatory B-cells that could maintain long term immune tolerance.

Identifiants

pubmed: 33045883
doi: 10.2217/imt-2020-0189
doi:

Substances chimiques

Immunologic Factors 0
Rituximab 4F4X42SYQ6

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

35-53

Auteurs

Gérôme Bohelay (G)

Department of Dermatology, Groupe Hospitalier Paris Seine-Saint-Denis, AP-HP & INSERM UMR1125, Bobigny, France.

Frédéric Caux (F)

Department of Dermatology, Groupe Hospitalier Paris Seine-Saint-Denis, AP-HP & INSERM UMR1125, Bobigny, France.

Philippe Musette (P)

Department of Dermatology, Groupe Hospitalier Paris Seine-Saint-Denis, AP-HP & INSERM UMR1125, Bobigny, France.

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Classifications MeSH