Anti-phospholipid IgG antibodies detected by line immunoassay differentiate patients with anti-phospholipid syndrome and other autoimmune diseases.

ABSTRACT: Anti-phospholipid antibodies (aPL) analyzed by line immunoassay (LIA) can recognize beta2-glycoprotein I (?2GPI) domain 1 (D1) epitopes depending on ?2GPI binding to distinct phospholipids. The aPL LIA was compared with consensus ELISA to investigate whether both techniques can discriminate anti-phospholipid syndrome (APS) patients from aPL-positive, systemic autoimmune rheumatic diseases (SARD) patients without clinical symptoms of APS and controls.Thirty-four APS patients (14 arterial/venous thrombosis, 16 pregnancy morbidity, and 4 both), 41 patients with SARD lacking clinical APS criteria but demonstrating positivity for anti-?2GPI (a?2GPI) IgG, and 20 healthy subjects (HS) were tested for aPL to cardiolipin (aCL), phosphatidic acid, phosphatidylcholine, phosphatidylethanolamine, phosphatidylglycerol (aPG), phosphatidylinositol, phosphatidylserine, ?2GPI, prothrombin, and annexin V by LIA. Samples were also tested for aCL, a?2GPI, a?2GPI-domain 1 (aD1), and a?2GPI-domains 4-5 (aD4-5) by ELISA and for lupus anti-coagulant.Comparison of LIA with ELISA revealed a good agreement for the consensus criteria aPL a?2GPI and aCL IgG (kappa?=?0.69, 0.68, respectively) and a moderate agreement for IgM (kappa?=?0.52, 0.49, respectively). Regarding ELISA, aD1/aD4-5 demonstrated the best performance of differentiating APS from asymptomatic SARD [area under the curve (AUC): 0.76]. aPG IgG had the best performance by LIA (AUC: 0.72) not significantly different from aD1/aD4-5. There was a good agreement for aPG IgG with aD1/aD4-5 (kappa?=?0.71).aD1/aD4-5 (ELISA) and aPG IgG (LIA) differentiate APS from SARD patients. PG appears to interact with ?2GPI of APS patients and exposes D1 thereof for disease-specific aPL binding in LIA.

SUBMITTER: Nalli C 

PROVIDER: S-EPMC5975024 | biostudies-other | 2018 May

REPOSITORIES: biostudies-other