Phospholipid dependent antibodies are usually measured with assays for
antiphosholipid/anticardiolipin antibodies (aPLA) or for lupus antico
agulant (LA) activity. Most of them are targeted to complexes of beta(
2)-glycoprotein I (beta(2)-GPI) and anionic phospholipds (PLP) or to p
rothrombin for some LA. New understandings allow a better standardisat
ion and optimisation of assays' reactivity. Antigenic targets of phosp
holipid dependent antibodies were studied on plasmas from 38 patients
with the antiphospholipid syndrome (APS) and presenting aPLA and/or LA
. Using human beta(2)-GPI-PLP complexes as solid phase antigen offers
the highest sensitivity for measuring aPLA. Many aPLA, but not all, al
so react with beta(2)-GPI coated on solid phase, however there is no e
vidence until now that this latter reactivity shows a closest associat
ion with the clinical context. Most of the patients with LA present an
immunological reactivity to beta(2)-GPI alone or to prothrombin, when
these proteins are coated on solid phase. In two cases there was a re
activity to only beta(2)-GPI-PLP complexes. For the various immunoassa
ys, using NUNC type I plates offers a good binding capacity For coatin
g antigens. They are then present at enough density on solid phase for
insuring an efficient binding of autoantibodies. This is an important
factor for assay sensitivity and reproducibility. Interestingly, in 1
case with LA, autoantibodies were reactive with coated beta(2)-GPI al
one but not with its PLP-complexes. In another case reactivity to beta
(2)-GPI was much higher than that to beta(2)-GPI-PLP.