Emerging therapy options for IgG4-related disease.


Journal

Expert review of clinical immunology
ISSN: 1744-8409
Titre abrégé: Expert Rev Clin Immunol
Pays: England
ID NLM: 101271248

Informations de publication

Date de publication:
05 2021
Historique:
pubmed: 11 3 2021
medline: 3 3 2022
entrez: 10 3 2021
Statut: ppublish

Résumé

Awareness of IgG4-related disease (IgG4-RD) is increasing worldwide and specialists are now familiar with most of its clinical manifestations and mimickers. IgG4-RD promptly responds to glucocorticoids and repeated courses are typically used to induce and maintain remission because the disease relapses in most patients. If left untreated, it can lead to organ dysfunction, organ failure and death. Advancement in our understanding of IgG4-RD pathogenesis is leading to the identification of novel therapeutic targets and emerging treatments are now setting the stage for personalized therapies for the future. This review focuses on emerging treatment options for IgG4-RD based on our advancing understanding of disease pathophysiology. Research was performed in the English literature on Pubmed and clinicaltrials.gov databases. Glucocorticoids remain the first-line induction treatment for the multi-organ manifestations of IgG4-RD. Alternative immunosuppressive agents for maintaining remission are warranted in order to avoid long-term steroid toxicity, and to offer a more mechanistic and personalized therapeutic strategy. Targeting B and T-lymphocyte activation represents the most promising approach, but randomized controlled trials are eagerly awaited to confirm positive preliminary experiences reported in case series and small cohort studies.

Identifiants

pubmed: 33689549
doi: 10.1080/1744666X.2021.1902310
doi:

Substances chimiques

Glucocorticoids 0
Immunoglobulin G 0
Immunosuppressive Agents 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

471-483

Auteurs

Marco Lanzillotta (M)

Università Vita-Salute San Raffaele, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Unit of Immunology, Rheumatology, Allergy and Rare Diseases (Unirar), IRCCS San Raffaele Scientific Institute, ss Milan, Italy.

Andreu Fernàndez-Codina (A)

Internal Medicine Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Rheumatology Division and General Internal Medicine division-Windsor Campus, Western University, 268 Grosvenor St, D2-191, Rheumatology Centre, St. Joseph´s Health Care, London, Ontario, Canada.

Emma Culver (E)

Translational Gastroenterology Unit, University of Oxford, Oxford,UK.
Hepatology, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.

Mikael Ebbo (M)

Département De Médecine Interne, Centre De Référence Constitutif Des Cytopénies Auto-immunes De L'adulte (CERECAI), Hôpital De La Timone, Aix-Marseille Université, Assistance publique-Hôpitaux De Marseille, Marseille, France.

Fernando Martinez-Valle (F)

Internal Medicine Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.

Nicolas Schleinitz (N)

Département De Médecine Interne, Centre De Référence Constitutif Des Cytopénies Auto-immunes De L'adulte (CERECAI), Hôpital De La Timone, Aix-Marseille Université, Assistance publique-Hôpitaux De Marseille, Marseille, France.

Emanuel Della-Torre (E)

Università Vita-Salute San Raffaele, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Unit of Immunology, Rheumatology, Allergy and Rare Diseases (Unirar), IRCCS San Raffaele Scientific Institute, ss Milan, Italy.

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Classifications MeSH