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甲型血友病患者诱导对凝血因子VIII产生耐受性后出现的非凝血抑制性凝血因子VIII抗体。

Noncoagulation inhibitory factor VIII antibodies after induction of tolerance to factor VIII in hemophilia A patients.

作者信息

Nilsson I M, Berntorp E, Zettervall O, Dahlbäck B

机构信息

Department of Coagulation Disorders, University of Lund, Malmö General Hospital, Sweden.

出版信息

Blood. 1990 Jan 15;75(2):378-83.

PMID:2104765
Abstract

We recently described tolerance induction with factor VIII/IX, cyclophosphamide, and high-dose intravenous IgG in hemophilia A or B patients with coagulation inhibitory antibodies. Circulating noninhibitory antibodies complexed with factor IX have been demonstrated in tolerant hemophilia B patients. Similar findings are now described in six tolerant hemophilia A patients. Complexes between factor VIII and the 'tolerant' antibody were demonstrated by subjecting plasma to gel filtration chromatography, void fractions containing factor VIII/vWF complexes being collected and adsorbed to protein A. Using 125I-labeled F(ab')2 fragments against IgG subclass and factor VIII antigen, complexes between an IgG4 antibody and factor VIII were found to adsorb to protein A. After infusion of factor VIII to tolerant patients, all factor VIII circulated in complex with IgG4 antibody. In three of the patients, the 'tolerant' antibodies inhibited an ELISA specific for factor VIII light chain but, unlike the pretolerant antibodies, did not bind radiolabeled factor VIII heavy chain. Although after induction of tolerance the patients still have circulating IgG4 antibodies against factor VIII, the antibodies differ in specificity, lack coagulation inhibitory activity, and do not enhance the rate of elimination of factor VIII.

摘要

我们最近描述了在患有凝血抑制性抗体的甲型或乙型血友病患者中,使用凝血因子VIII/IX、环磷酰胺和大剂量静脉注射免疫球蛋白诱导耐受性的情况。在耐受性乙型血友病患者中已证实存在与凝血因子IX结合的循环非抑制性抗体。现在在6例耐受性甲型血友病患者中也发现了类似的结果。通过对血浆进行凝胶过滤色谱法,证明了凝血因子VIII与“耐受性”抗体之间形成复合物,收集含有凝血因子VIII/vWF复合物的空体积组分并吸附到蛋白A上。使用针对IgG亚类和凝血因子VIII抗原的125I标记的F(ab')2片段,发现IgG4抗体与凝血因子VIII之间的复合物可吸附到蛋白A上。给耐受性患者输注凝血因子VIII后,所有凝血因子VIII均与IgG4抗体形成复合物循环。在3例患者中,“耐受性”抗体抑制了针对凝血因子VIII轻链的ELISA,但与耐受性前的抗体不同,不结合放射性标记的凝血因子VIII重链。尽管诱导耐受性后患者仍有针对凝血因子VIII的循环IgG4抗体,但这些抗体在特异性上有所不同,缺乏凝血抑制活性,并且不会提高凝血因子VIII的清除率。

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