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首页> 外文期刊>Immunologic Research: A Selective Reference to Current Research and Practice >Cross-reactivity between annexin A2 and Beta-2-glycoprotein I in animal models of antiphospholipid syndrome
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Cross-reactivity between annexin A2 and Beta-2-glycoprotein I in animal models of antiphospholipid syndrome

机译:抗磷脂综合征的动物模型中吞咽A2和β-2-糖蛋白I之间的交叉反应性

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Abstract Antiphospholipid syndrome (APS) affects coagulation and the brain by autoimmune mechanisms. The major antigen in APS is beta-2-glycoprotein I (β2-GPI) is known to complex with annexin A2 (ANXA2), and antibodies to ANXA2 have been described in APS. We measured these antibodies in mice with experimental APS (eAPS) induced by immunization with β2-GPI. Sera of these mice reacted significantly with recombinant ANXA2 by enzyme-linked immunosorbent assay (ELISA) and the eAPS mice had significantly high levels of immunoglobulin G (IgG) in the brain by immunoblot assays compared to adjuvant immunized controls. Immunoprecipitation performed by mixing eAPS brain tissue with protein-G beads resulted in identification of two autoantigens unique to the eAPS group, one of which was ANXA2. In order to study more directly and methodically the specific role of anti-ANXA2 antibodies in APS, we immunized mice with β2-GPI which contained no ANXA2 or with ANXA2 and measured antibodies to these proteins. Levels of antibodies to ANXA2 measured by ELISA were 0.72?±?0.007 arbitrary units (a.u), 0.24?±?0.03 and 0.02?±?0.01?a.u for sera from ANXA2, β2-GPI and control mice, respectively ( p ??0.0001 and p ?=?0.037 for the comparison of the ANXA2 and β2-GPI groups to the controls). Purified IgG from β2-GPI sera did not show cross-binding with ANXA2. Antibodies to β2-GPI and phospholipids were found in the β2-GPI immunized group only. The present study suggests an immune response to the β2-GPI–ANXA2 complex in eAPS and provides a novel ANXA2 immunization model which will serve to study the role of ANXA2 antibodies in of APS. ]]>
机译:摘要抗磷脂综合征(APS)通过自身免疫机制影响凝血和脑。 APS中的主要抗原是β-2-糖蛋白I(β2-GPI)是已知的,并且在Anxxin A2(ANXA2)中已知复合,并且已经在APS中描述了对ANXA2的抗体。我们测量了通过用β2-GPI免疫诱导的实验APS(EAPS)的小鼠中的这些抗体。通过酶联免疫吸附试验(ELISA),这些小鼠的血清具有显着的反应,通过酶联免疫吸附测定(ELISA),并且通过免疫印迹测定与佐剂免疫控制相比,EAPS小鼠通过免疫印迹测定具有显着高水平的免疫球蛋白G(IgG)。通过将EAPS脑组织与蛋白-G珠子混合来进行免疫沉淀,导致鉴定EAPS组独一无二的两种自身抗原,其中一个是ANXA2。为了更直接和有条不紊地研究APS中抗ANXA2抗体的特定作用,我们用β2-GPI的小鼠免疫小鼠,其含有ANXA2或ANXA2并测量这些蛋白质的抗体。通过ELISA测量的ANXA2的抗体水平为0.72〜±0.007个任意单位(Au),0.24〜±0.03和0.02?0.01〜0.01?0.01?0.01〜0.Su,用于来自ANXA2,β2-GPI和对照小鼠的血清(P?&lt ;α0.0001和p?= 0.037,用于对照组织和β2-GPI组进行比较)。来自β2-GPI血清的纯化IgG未显示与ANXA2的交叉结合。在β2-GPI免疫基团中发现β2-GPI和磷脂的抗体。本研究表明,对EAPS中β2-GPI-ANXA2复合物的免疫应答,并提供了一种新的ANXA2免疫模型,可以用于研究APS中的ANXA2抗体的作用。 ]]>

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