Alteration of the aPA ELISA by UV exposure of polystyrene microtiter plates

Interlaboratory inconsistencies in antiphospholipid antibody (aPA) solid phase assays have prompted controversy in clinical laboratory testing for aPA. We found that the aPA ELISA can be influenced by the type of microtiter plate utilized and by the conditions in which the plates are stored. By exposing 96-well, flat-bottom polystyrene microtiter plates to short wave UV light (254 nm), the aPA ELISA signal decreased in a UV dose-dependent manner. No effect was seen with long wave UV light (366 nm). These results were independent of the antibody isotype under study or the phospholipid (PL) antigen used: anionic phosphatidylserine (PS) and cardiolipin (CL), or zwitterionic phosphatidylethanolamine (PE). Purified human beta(2)-glycoprotein I (beta(2)GPI), a known cofactor for anionic PL, and rabbit anti-beta 2GPI antisera were used to demonstrate that beta(2)GPI bound equally to UV treated and untreated microtiter plates. In contrast, recognition of beta(2)GPI on an anionic PL surface was decreased on UV treated plates, suggesting that UV exposure alters the lipid binding properties of the microtiter plate. To determine whether UV exposure inhibited PL binding directly or caused a change in the way the PL was bound, the amount of PL bound to UV treated and untreated plates was measured by using fluorescent labeled PS and a fluorimeter. PS binding was decreased by 53% in UV treated wells as compared to untreated wells. These data show that short wave UV exposure reduces PL binding to polystyrene microtiter plates, thereby reducing the amount of beta(2)GPI bound to PL coated ELISA plates. Thus by using UV exposed microtiter plates, decreased or false-negative aPA ELISA results may be obtained for aPA positive plasmas. (C) 1996 Wiiey-Liss, Inc.