B lymphocytes in abdominal aortic aneurysms

Atherosclerosis. 2015 Sep;242(1):311-7. doi: 10.1016/j.atherosclerosis.2015.07.036. Epub 2015 Jul 21.

Abstract

Abdominal aortic aneurysm (AAA) is a progressive inflammatory disease of the artery walls. Immune cells, including B lymphocytes, are implicated in the pathogenesis of AAA through interconnected mechanisms. Many studies have shown that compared with normal abdominal aortic tissue, the amount of B lymphocytes that infiltrate the adventitia of AAAs was significantly higher. Activated B lymphocytes promote AAA by producing immunoglobulins, cytokines, and matrix metalloproteinases (MMPs), resulting in the activation of macrophages, mast cells (MCs) and complement pathways. Finally, all of these factors lead to the degradation of collagen and matrix proteins and to aortic wall remodeling, which are hallmarks of AAA. However, few studies focus on the relative function of B cells, and their precise mechanisms in AAA remain unclear. Thus, we summarize the current knowledge on the role of B cells in AAA and offer recommendations for further investigation of preventing the progression of AAA.

Keywords: Aortic aneurysm; B lymphocyte; Cytokine; Immunoglobulin; Pathogenesis.

Publication types

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

MeSH terms

  • Animals
  • Aorta, Abdominal / immunology*
  • Aorta, Abdominal / metabolism
  • Aorta, Abdominal / pathology
  • Aortic Aneurysm, Abdominal / immunology*
  • Aortic Aneurysm, Abdominal / metabolism
  • Aortic Aneurysm, Abdominal / pathology
  • B-Lymphocytes / immunology*
  • B-Lymphocytes / metabolism
  • B-Lymphocytes / pathology
  • Cytokines / immunology
  • Cytokines / metabolism
  • Disease Progression
  • Humans
  • Immunoglobulin G / immunology
  • Immunoglobulin G / metabolism
  • Inflammation Mediators / immunology
  • Inflammation Mediators / metabolism
  • Matrix Metalloproteinases / immunology
  • Matrix Metalloproteinases / metabolism
  • Signal Transduction

Substances

  • Cytokines
  • Immunoglobulin G
  • Inflammation Mediators
  • Matrix Metalloproteinases