Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P02749 (
beta2-glycoprotein I
)
836
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
We studied sera from patients with various disorders including collagen diseases, Buerger's disease, deep vein thrombosis, repeated abortions and idiopathic thrombocytopenic purpura in order to measure anticardiolipin antibody (aCL) titers. In our assay system, we can detect aCL against bovine cardiolipin and the complex of cardiolipin and
beta 2-glycoprotein I
(
beta 2-GPI
). This was done with simultaneous assays using blank wells and bovine cardiolipin coated wells in the
EIA
method in which both wells were also coated with bovine serum albumin possibly containing
beta 2-GPI
, then aCL titers was given by subtraction of O.D. values of blank wells from those of cardiolipin coated wells. When the aCL was quantified by anti human immunoglobulin antibodies, collagen diseases showed positive aCL in 15 (11.5%) out of 130 sera with positive anti ENA antibodies, 3 (11.1%) out of 27 sera with positive anti DNA antibodies and 3 (5.2%) out of 58 sera with other positive ANA sera. The other hand, we found positive aCL in 2 (4.9%) out of 41 sera from patients with Buerger's disease, 4 (36.4%) out of 11 sera from patients with deep vein thrombosis, 1 (7.7%) out of 13 sera from patients with repeated abortions and 6 (14.6%) out of 41 sera from patients with idiopathic thrombocytopenic purpura. Twenty one (61.8%) out of these aCL positive sera had also positive IgG-aCL for the assay using anti human IgG antibody. Compared to previous reports, we thought, low incidence of aCL in our study was due to exclusion of anti
beta 2-GPI
antibody in our assay system.
...
PMID:[Detection of anticardiolipin antibody using the EIA kit prepared to eliminate interference of serum cofactor]. 837 6
Cardiolipin binding of IgG-class anticardiolipin antibody (aCL) depends on the existence of
beta 2-glycoprotein I
(
beta 2-GPI
). We developed an
EIA
system that enables detection of antibodies against
beta 2-GPI
, without the presence of cardiolipin. This system involves use of irradiated polystyrene plates, in which oxygen atoms are introduced onto the surfaces of the plates.
beta 2-GPI
bound to the surface of these plates is assumed to undergo a conformational change that exposes normally cryptic epitopes. Anti-
beta 2-GPI
antibody measured using this
EIA
system showed good correlation with aCL measured by conventional
EIA
methods and may prove useful in evaluating the risk of thrombosis and monitoring the clinical course in patients with SLE. Utilizing this
EIA
system and
beta 2-GPI
-deleted mutants, we found that the fourth domain of
beta 2-GPI
is involved in expression of one of the cryptic epitopes recognized by aCL. We also found that oxidized LDL are sequentially targeted by
beta 2-GPI
and aCL.
...
PMID:Anti-beta 2-glycoprotein I antibody: specificity and clinical significance. 890 64