Detection of intracellular cytokines during antioxidant supplementation incorticoid-dependent asthmatics and modulation of adhesion molecule expression on cultured endothelial cells

Citation
M. Horvathova et al., Detection of intracellular cytokines during antioxidant supplementation incorticoid-dependent asthmatics and modulation of adhesion molecule expression on cultured endothelial cells, BIOL TR EL, 83(1), 2001, pp. 17-30
Citations number
68
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
BIOLOGICAL TRACE ELEMENT RESEARCH
ISSN journal
01634984 → ACNP
Volume
83
Issue
1
Year of publication
2001
Pages
17 - 30
Database
ISI
SICI code
0163-4984(200110)83:1<17:DOICDA>2.0.ZU;2-R
Abstract
In this study, we report on the interferon-gamma (IFN-gamma) and interleuki n-4 (IL-4) cytokine responses to phorbol myristate acetate (PMA) + ionomyci n-stimulated CD3+ lymphocytes in asthmatic subjects when compared with norm al donors. There was a significantly lower production of intracellular IFN- gamma in asthmatic patients. No difference was found for IL-4 production be tween these two groups. After administration of a multivitamin-mineral supplement containing seleni um, zinc, vitamin A, vitamin B-6, vitamin C, and vitamin E for 6 mo, a sign ificant increase in the percentage of CD3+/IL-4 positive cells (p < 0.05) w as found. The induction of endothelial cell adhesion molecule (CAM) expression in cul tured human umbilical vein endothelial cells (HUVEC) and whole-blood mixtur e was studied using flow cytometry. The ICAM-1 and VCAM-1 expressions were higher in the patients than in control donors (p < 0.05). There is a correl ation between the increased percentage of CD3+/IFN-gamma positive cells and reduced endothelial ICAM-1 and VCAM-1 expression after 6 mo of interventio n period. No apparent effect of supplementation on CAM expression was found , suggesting that these changes do not arise from an antioxidant mechanism. This newly developed whole-blood technique for the assessment of CAM expre ssion can be of use for monitoring therapy in inflammatory diseases.