Circulating immunoglobulins are not associated with intraplaque mast cell number and other vulnerable plaque characteristics in patients with carotid artery stenosis

PLoS One. 2014 Feb 21;9(2):e88984. doi: 10.1371/journal.pone.0088984. eCollection 2014.

Abstract

Background: Recently, we have shown that intraplaque mast cell numbers are associated with atherosclerotic plaque vulnerability and with future cardiovascular events, which renders inhibition of mast cell activation of interest for future therapeutic interventions. However, the endogenous triggers that activate mast cells during the progression and destabilization of atherosclerotic lesions remain unidentified. Mast cells can be activated by immunoglobulins and in the present study, we aimed to establish whether specific immunoglobulins in plasma of patients scheduled for carotid endarterectomy were related to (activated) intraplaque mast cell numbers and plasma tryptase levels. In addition, the levels were related to other vulnerable plaque characteristics and baseline clinical data.

Methods and results: OxLDL-IgG, total IgG and total IgE levels were measured in 135 patients who underwent carotid endarterectomy. No associations were observed between the tested plasma immunoglobulin levels and total mast cell numbers in atherosclerotic plaques. Furthermore, no associations were found between IgG levels and the following plaque characteristics: lipid core size, degree of calcification, number of macrophages or smooth muscle cells, amount of collagen and number of microvessels. Interestingly, statin use was negatively associated with plasma IgE and oxLDL-IgG levels.

Conclusions: In patients suffering from carotid artery disease, total IgE, total IgG and oxLDL-IgG levels do not associate with plaque mast cell numbers or other vulnerable plaque histopathological characteristics. This study thus does not provide evidence that the immunoglobulins tested in our cohort play a role in intraplaque mast cell activation or grade of atherosclerosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carotid Stenosis / immunology*
  • Carotid Stenosis / pathology*
  • Endarterectomy, Carotid
  • Humans
  • Immunoglobulin E / blood*
  • Immunoglobulin G / blood*
  • Immunohistochemistry
  • Lipoproteins, LDL / blood
  • Mast Cells / immunology*
  • Statistics, Nonparametric

Substances

  • Immunoglobulin G
  • Lipoproteins, LDL
  • oxidized low density lipoprotein
  • Immunoglobulin E

Grants and funding

This research forms part of the Project P1.03 PENT of the research program of the BioMedical Materials Institute, co-funded by the Dutch Ministry of Economic Affairs, Agriculture and Innovation. DvdV was financed by the LCTD3 program. We acknowledge the support from the Netherlands CardioVascular Research Initiative: the Dutch Heart Foundation, Dutch Federation of University Medical Centres, the Netherlands Organisation for Health Research and Development and the Royal Netherlands Academy of Sciences, for the GENIUS project “Generating the best evidence-based pharmaceutical targets for atherosclerosis” (CVON2011-19). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.