Lai J D, Lillicrap D
Department of Pathology & Molecular Medicine, Queen's University, Kingston, ON, Canada.
Int J Lab Hematol. 2017 May;39 Suppl 1:6-13. doi: 10.1111/ijlh.12659.
In the treatment of hemophilia A, the 20%-30% risk of developing of anti-factor VIII (FVIII) antibodies, or inhibitors, is the dominant concern among healthcare providers. Immune tolerance induction remains the only effective method of eradicating inhibitors in approximately 75% of patients, but is accompanied by significant emotional and economical burden. While certain risk factors, such as the type of FVIII mutation, offer some insight, there remains no strategy to confidently predict the development of an inhibitor. Moreover, even if such a predictive tool existed, there is currently no proven protocol for tolerance induction of a previously untreated patient. In recent years, the growing body of knowledge concerning the fundamental immunology of inhibitors has shed light on potential therapeutic interventions. In this review, we highlight these new findings and their influences on translational medicine.
在甲型血友病的治疗中,医疗服务提供者主要关注的是有20%-30%的患者会产生抗凝血因子VIII(FVIII)抗体或抑制剂。免疫耐受诱导仍然是消除约75%患者体内抑制剂的唯一有效方法,但会带来巨大的情感和经济负担。虽然某些风险因素,如FVIII突变类型,能提供一些线索,但目前仍没有可靠的策略来预测抑制剂的产生。此外,即使存在这样一种预测工具,目前也没有经过验证的针对既往未治疗患者的耐受诱导方案。近年来,关于抑制剂基础免疫学的知识不断增加,为潜在的治疗干预提供了线索。在本综述中,我们重点介绍这些新发现及其对转化医学的影响。