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The soluble forms of CD28, CD86 and CTLA-4 constitute possible immunological markers in patients with abdominal aortic aneurysm.

Authors :
Sakthivel P
Shively V
Kakoulidou M
Pearce W
Lefvert AK
Source :
Journal of internal medicine [J Intern Med] 2007 Apr; Vol. 261 (4), pp. 399-407.
Publication Year :
2007

Abstract

Objective: The T cell co-stimulatory factors CD28 and CTLA-4 and their ligands CD80 and CD86 occur as receptors on T cells and antigen-presenting cells and also in soluble forms in the circulation. We determined the levels of soluble co-stimulatory molecules in patients with abdominal aortic aneurysm (AAA) and normal individuals. We further correlated these soluble co-stimulatory molecules to other clinical parameters of importance such as age of the patient, presence of hypertension, size of the aneurysm and levels of matrix metalloproteinases-9 and C-reactive protein.<br />Design, Setting, Subjects: This case-control study was designed to quantify the circulating levels of soluble co-stimulatory molecules by an in-house enzyme linked immunosorbent assay. A total of 314 subjects participated in the study including 100 patients and 214 normal controls. The statistical analysis was performed by Mann-Whitney test and Spearman's correlation rank test.<br />Results: Our results show increased plasma levels of sCD28, sCD86 (P = 0.0001) and decreased plasma levels of sCTLA-4 (P = 0.0018) in the patients compared with normal individuals. The levels of these factors were not related to the age of the patient, size of aneurysm or levels of C-reactive protein in plasma. There was, however, a significant inverse relationship between the concentrations of sCTLA-4 and sCD80 with matrix metalloproteinase-9.<br />Conclusions: We suggest that soluble co-stimulatory molecules serve as biomarkers for the estimation of immune activation in AAA patients.

Details

Language :
English
ISSN :
0954-6820
Volume :
261
Issue :
4
Database :
MEDLINE
Journal :
Journal of internal medicine
Publication Type :
Academic Journal
Accession number :
17391115
Full Text :
https://doi.org/10.1111/j.1365-2796.2007.01773.x