Novel immune assay for quantification of plasma protective capacity against oxidized phospholipids

Author:

Bochkov Valery1,Schoenenberger Andreas W2,Oskolkova Olga1,Toth Ursula3,Stöckl Johannes4,Majdic Otto4,Daci Armond35,Resink Thérèse J6,Erne Paul6,Philippova Maria6

Affiliation:

1. Institute of Pharmaceutical Sciences, University of Graz, Austria

2. Division of Geriatrics, Department of General Internal Medicine, Inselspital, Bern University Hospital & University of Bern, Bern, Switzerland

3. Department of Vascular Biology & Thombosis Research, Medical University of Vienna, Vienna, Austria

4. Institute of Immunology, Medical University of Vienna, Vienna, Austria

5. Department of Pharmacy, Faculty of Medicine, University of Prishtina, Kosovo

6. Signaling Laboratory, Department of Biomedicine, Basel University Hospital, Basel, Switzerland

Abstract

Aim: Oxidized phospholipids (OxPL) are the major pathogenic component of oxidized low-density lipoproteins (OxLDL). Endogenous anti-OxPL activity, defined as the ability to neutralize adverse effects of oxidized lipids, may have biomarker potential. Methods & results: Using two anti-OxPL monoclonal antibodies (commercial mAB-E06 and custom mAB-509) we developed a novel ELISA that measures the global capacity of plasma to inactivate OxPL. Preincubation of OxLDL with plasma inhibits its binding of anti-OxPL mABs. This phenomenon (‘masking’) reflects anti-OxPL plasma activity. A pilot clinical application of the assay revealed reduced anti-OxPL activity in hypertension, coronary artery disease, acute coronary syndrome and diabetes. Conclusion: Inadequate anti-OxPL protection may contribute to cardiovascular disease and have biomarker potential in conditions associated with abnormal lipid peroxidation.

Publisher

Future Medicine Ltd

Subject

Biochemistry, medical,Clinical Biochemistry,Drug Discovery

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