Orstavik K H
Department of Medical Genetics, Ullevål Hospital, Oslo, Norway.
Folia Haematol Int Mag Klin Morphol Blutforsch. 1990;117(4):545-8.
Five per cent of patients with haemophilia B develop inhibitors to factor IX. It is of interest to know the immunoglobulin subclass of these IgG antibodies. We have developed a sensitive method for the characterization of the subclass nature of inhibitors to factor IX. The technique is a crossed immunoelectrophoresis for the isolation of factor IX-inhibitor complexes followed by an enzyme-linked immunoassay using monoclonal antibodies to IgG subclasses for the subclass identification. We studied seven inhibitors with both low and high titres. One patient was studied at a very early stage of inhibitor development. All inhibitors gave a strong reaction with antibody to IgG4. Depending on the titre of the inhibitor, a reaction was also found with antibodies to IgG1 and IgG2. No inhibitor contained any detectable IgG3. IgG4 does not bind complement and it is therefore of importance that IgG4 is the main subclass both in high-titred and in low-titred inhibitors. The inhibitors are polyclonal antibodies, also at an early stage of inhibitor development.
5%的乙型血友病患者会产生针对凝血因子IX的抑制物。了解这些IgG抗体的免疫球蛋白亚类很有意义。我们开发了一种灵敏的方法来鉴定针对凝血因子IX抑制物的亚类性质。该技术是一种交叉免疫电泳,用于分离凝血因子IX - 抑制物复合物,随后使用针对IgG亚类的单克隆抗体进行酶联免疫测定以鉴定亚类。我们研究了7种低滴度和高滴度的抑制物。对一名患者在抑制物产生的非常早期阶段进行了研究。所有抑制物与抗IgG4抗体均产生强烈反应。根据抑制物的滴度,还发现与抗IgG1和IgG2抗体有反应。未检测到任何抑制物含有IgG3。IgG4不结合补体,因此,无论是高滴度还是低滴度的抑制物中IgG4都是主要亚类,这一点很重要。这些抑制物是多克隆抗体,在抑制物产生的早期阶段也是如此。