Therapeutic Avenues to Modulate B-Cell Function in Patients With Cardiovascular Disease

Author:

O’Brien James W.1ORCID,Case Ayden1ORCID,Kemper Claudia2ORCID,Zhao Tian X.13,Mallat Ziad14ORCID

Affiliation:

1. Division of Cardiorespiratory Medicine, Department of Medicine, Victor Phillip Dahdaleh Heart and Lung Research Institute, University of Cambridge, United Kingdom (J.W.O., A.C., T.X.Z., Z.M.).

2. Complement and Inflammation Research Section, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD (C.K.).

3. Department of Cardiology, Royal Papworth Hospital, Cambridge, United Kingdom (T.X.Z.).

4. Unversité de Paris, Inserm U970, Paris Cardiovascular Research Centre, France (Z.M.).

Abstract

The adaptive immune system plays an important role in the development and progression of atherosclerotic cardiovascular disease. B cells can have both proatherogenic and atheroprotective roles, making treatments aimed at modulating B cells important therapeutic targets. The innate-like B-cell response is generally considered atheroprotective, while the adaptive response is associated with mixed consequences for atherosclerosis. Additionally, interactions of B cells with components of the adaptive and innate immune system, including T cells and complement, also represent key points for therapeutic regulation. In this review, we discuss therapeutic approaches based on B-cell depletion, modulation of B-cell survival, manipulation of both the antibody-dependent and antibody-independent B-cell response, and emerging immunization techniques.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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