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Antibodies toward High‐Density Lipoprotein Components Inhibit Paraoxonase Activity in Patients with Systemic Lupus Erythematosus
Author(s) -
BATUCA J. R.,
AMES P. R. J.,
ISENBERG D. A.,
DELGADO ALVES J.
Publication year - 2007
Publication title -
annals of the new york academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.712
H-Index - 248
eISSN - 1749-6632
pISSN - 0077-8923
DOI - 10.1196/annals.1422.016
Subject(s) - paraoxonase , antibody , pon1 , medicine , immunology , titer , population , antibody titer , endocrinology , immune system , lipoprotein , cholesterol , oxidative stress , chemistry , biochemistry , environmental health , genotype , gene
: Patients with systemic lupus erythematosus (SLE) have an increased incidence of vascular disease, and oxidative stress is recognized as an important feature in this condition, despite the underlying mechanisms not being fully understood. In these patients, an interaction between lipoproteins and the immune system has been suggested, but most studies have only looked at antibodies against oxidized low‐density lipoproteins. This study was undertaken to determine the presence of antibodies directed against high‐density lipoproteins (HDL) and to identify a possible association between these antibodies and paraoxonase (PON), an antioxidant enzyme present in HDL. Plasma from 55 patients with SLE was collected and IgG aHDL and antiapolipoprotein A‐I (aApo A‐I) antibodies were assessed by enzyme‐linked immunosorbent assay. Standardization of the method was performed in a control population of 150 healthy subjects. Plasma levels above 5 standard deviations of the mean of the control population were considered positive. PON activity was assessed by quantification of p ‐nitrophenol formation (μmol/mL/min). Patients with SLE had higher titers of aHDL ( P < 0.0001) and aApo A‐I ( P < 0.0001) antibodies, and lower PON activity ( P < 0.0001) than healthy controls. There was also a direct correlation between the titers of aHDL and aApo A‐I antibodies ( r = 0.61; P < 0.0001). PON activity was inversely correlated with aApo A‐I ( P = 0.0129) antibody levels. Anti‐HDL and aApo A‐I antibodies from patients with high titers were isolated and subsequently incubated with human HDL. These antibodies reduced PON activity up to a maximum of 70.2% and 78.4%, respectively. This study showed the presence of aHDL and aApo A‐I antibodies in patients with SLE. These antibodies were associated with reduced PON activity in plasma, and the in vitro inhibition assay confirmed a direct inhibition of the enzyme activity.