Astermark J
Department for Coagulation Disorders, Malmö University Hospital, Malmö, Sweden.
Haemophilia. 2006 Jul;12 Suppl 3:52-60. doi: 10.1111/j.1365-2516.2006.01261.x.
The formation of inhibitory alloantibodies is, in the postinfectious era, the most severe and costly complication of replacement therapy in patients with haemophilia. The complexity of the immune response to the infused factor becomes more and more obvious as knowledge in the area increases. Antibodies develop as a result of a complex multi-factorial interaction between antigen-presenting cells, T- and B-lymphocytes. Genetic susceptibility of cell surface molecules, such as the major histocompatibility complex, the T-cell receptor and cytokine receptors, as well as various immunomodulatory molecules have a major impact on the outcome. In addition, environmental factors probably influence the risk of inhibitor development. The current concept of inhibitor development is reviewed. A better understanding of the pathophysiological mechanisms involved will facilitate improvement of therapy in the future, and hopefully provide an opportunity to prevent this complication of treatment.
在感染后时代,抑制性同种抗体的形成是血友病患者替代治疗最严重且代价高昂的并发症。随着该领域知识的增加,针对输注因子的免疫反应的复杂性愈发明显。抗体的产生是抗原呈递细胞、T淋巴细胞和B淋巴细胞之间复杂多因素相互作用的结果。细胞表面分子的遗传易感性,如主要组织相容性复合体、T细胞受体和细胞因子受体,以及各种免疫调节分子,对结果有重大影响。此外,环境因素可能影响抑制剂形成的风险。本文综述了目前关于抑制剂形成的概念。更好地理解其中涉及的病理生理机制将有助于未来治疗的改进,并有望提供预防这种治疗并发症的机会。