Curry N S, Misbah S A, Giangrande P L F, Keeling D M
Oxford Haemophilia Centre and Thrombosis Unit, Oxford Radcliffe Hospitals, Oxford, UK.
Haemophilia. 2007 May;13(3):328-30. doi: 10.1111/j.1365-2516.2007.01463.x.
We describe a young boy with severe haemophilia B who developed inhibitory antibodies and an anaphylactoid reaction to factor IX. Immune tolerance was achieved by desensitisation with escalating doses of factor IX followed by the Malmö regimen.
我们描述了一名患有严重乙型血友病的小男孩,他产生了抑制性抗体,并对凝血因子IX发生类过敏反应。通过递增剂量的凝血因子IX脱敏,随后采用马尔默方案,实现了免疫耐受。