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免疫性和特发性中性粒细胞减少症。

Immune and idiopathic neutropenia.

作者信息

Dale D C

机构信息

Department of Medicine, University of Washington School of Medicine, Seattle 98195, USA.

出版信息

Curr Opin Hematol. 1998 Jan;5(1):33-6. doi: 10.1097/00062752-199801000-00006.

Abstract

Neutropenia is often attributed to immunologically mediated injury to mature neutrophils or their precursors. Clinically it is useful to classify immune mediated neutropenias as isoimmune, autoimmune (including some drug-associated neutropenias), and idiopathic (cases possibly with an immune mechanism). Isoimmune neutropenia occurs in infancy and the antigen and is an isoform of CD16. This condition usually resolves spontaneously. For other forms of immune neutropenia the antigens are not yet well defined and the diagnosis is usually based on clinical criteria. In these patients availability of granulocyte macrophage colony-stimulating factor is a major advance; most respond quickly to treatment with this growth factor.

摘要

中性粒细胞减少症通常归因于对成熟中性粒细胞或其前体的免疫介导损伤。临床上,将免疫介导的中性粒细胞减少症分为同种免疫性、自身免疫性(包括一些药物相关的中性粒细胞减少症)和特发性(可能具有免疫机制的病例)是有用的。同种免疫性中性粒细胞减少症发生于婴儿期,抗原是CD16的一种同种型。这种情况通常会自发缓解。对于其他形式的免疫性中性粒细胞减少症,抗原尚未明确界定,诊断通常基于临床标准。对于这些患者,粒细胞巨噬细胞集落刺激因子的应用是一项重大进展;大多数患者对这种生长因子治疗反应迅速。

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