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治疗性多特异性正常免疫球蛋白中存在针对自身抗体和VIII:C(抗血友病因子)同种抗体的抗独特型抗体。

Anti-idiotypes against autoantibodies and alloantibodies to VIII:C (anti-haemophilic factor) are present in therapeutic polyspecific normal immunoglobulins.

作者信息

Rossi F, Sultan Y, Kazatchkine M D

机构信息

INSERM U28, Hôpital Broussais, Paris, France.

出版信息

Clin Exp Immunol. 1988 Nov;74(2):311-6.

Abstract

Therapeutic, polyspecific, normal immunoglobulins (IVIg) suppress anti-factor VIII (VIII:C) activity of anti-VIII:c autoantibodies in vivo and in vitro. In the present study anti-VIII:C activity was found to be inhibited by two different preparations of IVIg in the plasma of three of four patients with autoantibodies and two of three patients with alloantibodies. F(ab')2 fragments from IVIg inhibited anti-VIII:C activity in F(ab')2 fragments from the plasma of the patients. In patients in whom anti-VIII:C activity was inhibited by IVIg, anti-VIII:C F(ab')2 antibodies were specifically retained on an affinity column of Sepharose-bound F(ab')2 from IVIg. In patients in whom anti-VIII:C activity was not suppressed by IVIg in vitro, no binding of anti-VIII:C antibodies to Sepharose-bound IVIg was observed. In a patient in whom anti-VIII:C activity was only suppressed by one preparation of IVIg, specific binding of anti-VIII:C antibodies was only observed with that preparation but not with another. These results indicate that IVIg contain anti-idiotypes against autoantibodies and alloantibodies to VIII:C. The capacity of IVIg to inhibit anti-VIII:C activity in vitro is directly related to the presence of demonstrable anti-idiotypes against anti-VIII:C antibodies. The finding of anti-idiotypes against anti-VIII:C alloantibodies in IVIg suggests that, in addition to autoantibodies, some alloantibodies may be suppressed in vivo by IVIg.

摘要

治疗性多特异性正常免疫球蛋白(静脉注射免疫球蛋白,IVIg)在体内和体外均可抑制抗凝血因子VIII(VIII:C)自身抗体的活性。在本研究中,发现4例自身抗体患者中的3例以及3例同种抗体患者中的2例,其血浆中的两种不同IVIg制剂可抑制VIII:C活性。IVIg的F(ab')2片段可抑制患者血浆F(ab')2片段中的抗VIII:C活性。在IVIg抑制抗VIII:C活性的患者中,抗VIII:C F(ab')2抗体特异性结合于IVIg的琼脂糖结合F(ab')2亲和柱上。在体外IVIg未抑制抗VIII:C活性的患者中,未观察到抗VIII:C抗体与琼脂糖结合的IVIg发生结合。在一名仅一种IVIg制剂可抑制抗VIII:C活性的患者中,仅观察到抗VIII:C抗体与该制剂特异性结合,与另一种制剂则未结合。这些结果表明,IVIg含有针对VIII:C自身抗体和同种抗体的抗独特型抗体。IVIg在体外抑制抗VIII:C活性的能力与可证明的针对抗VIII:C抗体的抗独特型抗体的存在直接相关。IVIg中存在针对抗VIII:C同种抗体的抗独特型抗体这一发现表明,除自身抗体外,某些同种抗体在体内也可能被IVIg抑制。

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