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获得性凝血因子VIII:C抑制剂的细胞毒性抑制作用

Cytotoxic suppression of acquired factor VIII:C inhibitors.

作者信息

Green D

机构信息

Department of Medicine, Northwestern University Medical School, Chicago, Illinois.

出版信息

Am J Med. 1991 Nov 4;91(5A):14S-19S. doi: 10.1016/s0002-9343(91)80142-9.

Abstract

Autoantibodies directed against factor VIII:C (FVIII:C) are associated with serious and often fatal bleeding. Efforts to suppress or abolish these antibodies with cytotoxic agents are frequently successful if antibody titer is not too high or there is an associated disease that undergoes remission. Corticosteroids alone may hasten antibody disappearance in almost half of patients, and cyclophosphamide is useful in those who are resistant to steroids administered alone or in combination. Patients refractory to these regimens may respond to a more aggressive approach using combination chemotherapy with cyclophosphamide, prednisone, and vincristine. Unfortunately, because of the rarity of this disorder, randomized, controlled trials have not been conducted either to compare treatments directly or to examine the factors presaging favorable outcomes. Recently, however, a multicenter trial comparing prednisone, cyclophosphamide, and the combination has been initiated, and some preliminary data from this investigation are presented. Approaches to the recognition and clinical management of this disorder also are described.

摘要

针对凝血因子VIII:C(FVIII:C)的自身抗体与严重且往往致命的出血有关。如果抗体滴度不太高或存在病情缓解的相关疾病,使用细胞毒性药物抑制或消除这些抗体的努力通常会成功。单独使用皮质类固醇可能会使近一半患者的抗体消失加速,而环磷酰胺对单独使用或联合使用类固醇耐药的患者有用。对这些治疗方案难治的患者可能对采用环磷酰胺、泼尼松和长春新碱联合化疗的更积极治疗方法有反应。不幸的是,由于这种疾病罕见,尚未进行随机对照试验来直接比较治疗方法或研究预示良好预后的因素。然而,最近启动了一项比较泼尼松、环磷酰胺及两者联合使用的多中心试验,并展示了该研究的一些初步数据。还描述了识别和临床管理这种疾病的方法。

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