Álvarez Teresa, Soto Immaculada, Astermark Jan
Department of Haematology, La Paz University Hospital, Madrid, Spain.
Eur J Haematol. 2015 Feb;94 Suppl 77:2-6. doi: 10.1111/ejh.12494.
The development of inhibitors is the most serious iatrogenic complication affecting patients with haemophilia. This complication is associated with impaired vital or functional prognosis, reduced quality of life and increased cost of treatment. The reasons why some patients develop antibodies to factor replacement and others do not remain unclear. It is however clear that inhibitor development results from a complex multifactorial interaction between genetic and non-genetic risk factors. Environmental influences implicated in increasing the risk of inhibitor formation can be viewed as modifiable risk factors. Therefore, identification of the non-genetic risk factors may offer the possibility of personalising haemophilia therapy by modifying treatment strategies in high-risk patients in the critical early phase of factor VIII exposure. In this article, we review the non-genetic factors reported as well as the potential impact of danger signals and the different scores for inhibitor development risk stratification.
抑制剂的产生是血友病患者面临的最严重的医源性并发症。这种并发症与重要脏器功能预后受损、生活质量下降以及治疗费用增加有关。部分患者会产生针对凝血因子替代治疗的抗体,而其他患者则不会,其原因尚不清楚。然而,抑制剂的产生显然是由遗传和非遗传风险因素之间复杂的多因素相互作用所致。与抑制剂形成风险增加相关的环境影响因素可被视为可改变的风险因素。因此,识别非遗传风险因素可能为在首次接触凝血因子VIII的关键早期阶段,通过调整高危患者的治疗策略来实现血友病治疗的个体化提供可能。在本文中,我们回顾了已报道的非遗传因素,以及危险信号的潜在影响和用于抑制剂产生风险分层的不同评分。