Autoantibodies and Cardiomyopathy: Focus on Beta-1 Adrenergic Receptor Autoantibodies.


Journal

Journal of cardiovascular pharmacology
ISSN: 1533-4023
Titre abrégé: J Cardiovasc Pharmacol
Pays: United States
ID NLM: 7902492

Informations de publication

Date de publication:
01 09 2022
Historique:
received: 21 10 2021
accepted: 16 03 2022
pubmed: 25 3 2022
medline: 9 9 2022
entrez: 24 3 2022
Statut: epublish

Résumé

Antibody response to self-antigens leads to autoimmune response that plays a determinant role in cardiovascular disease outcomes including dilated cardiomyopathy (DCM). Although the origins of the self-reactive endogenous autoantibodies are not well-characterized, it is believed to be triggered by tissue injury or dysregulated humoral response. Autoantibodies that recognize G protein-coupled receptors are considered consequential because they act as modulators of downstream receptor signaling displaying a wide range of unique pharmacological properties. These wide range of pharmacological properties exhibited by autoantibodies has cellular consequences that is associated with progression of disease including DCM. Increase in autoantibodies recognizing beta-1 adrenergic receptor (β1AR), a G protein-coupled receptor critical for cardiac function, is observed in patients with DCM. Cellular and animal model studies have indicated pathological roles for the β1AR autoantibodies but less is understood about the molecular basis of their modulatory effects. Despite the recognition that β1AR autoantibodies could mediate deleterious outcomes, emerging evidence suggests that not all β1AR autoantibodies are deleterious. Recent clinical studies show that β1AR autoantibodies belonging to the IgG3 subclass is associated with beneficial cardiac outcomes in patients. This suggests that our understanding on the roles the β1AR autoantibodies play in mediating outcomes is not well-understood. Technological advances including structural determinants of antibody binding could provide insights on the modulatory capabilities of β1AR autoantibodies in turn, reflecting their diversity in mediating β1AR signaling response. In this study, we discuss the significance of the diversity in signaling and its implications in pathology.

Identifiants

pubmed: 35323150
doi: 10.1097/FJC.0000000000001264
pii: 00005344-202209000-00005
pmc: PMC9452444
mid: NIHMS1791518
doi:

Substances chimiques

Autoantibodies 0
Receptors, Adrenergic, beta-1 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

354-363

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL089473
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL128382
Pays : United States

Informations de copyright

Copyright © 2022 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

The authors report no conflicts of interest.

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Auteurs

Wai Hong Wilson Tang (WHW)

Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland, OH; and.
Department of Cardiovascular Medicine, Heart, Vascular & Thoracic Institute, Cleveland Clinic, Cleveland, OH.

Sathyamangla V Naga Prasad (SV)

Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland, OH; and.

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