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严重联合免疫缺陷的家畜模型:犬X连锁严重联合免疫缺陷和马的严重联合免疫缺陷

Domestic animal models of severe combined immunodeficiency: canine X-linked severe combined immunodeficiency and severe combined immunodeficiency in horses.

作者信息

Felsburg P J, Somberg R L, Perryman L E

机构信息

Department of Clinical Studies, School of Veterinary Medicine, University of Pennsylvania, Philadelphia 19104.

出版信息

Immunodefic Rev. 1992;3(4):277-303.

PMID:1449787
Abstract

This review describes the clinical, immunologic and pathologic features of two naturally-occurring models of severe combined immunodeficiency (SCID) in domestic animals that represent different forms of human SCID. Canine X-linked SCID (XSCID) has an X-linked recessive mode of inheritance and, as such, represents a model for the most common form of human SCID in the United States. Affected dogs have normal percentages of circulating B cells and low to normal percentages of phenotypically mature, but nonfunctional T cells. Severe combined immunodeficiency in the horse is an autosomal recessive form of SCID that is characterized by a profound lymphopenia affecting both the B and T cell lineage most likely due to a lymphoid stem cell defect. Since these diseases are naturally-occurring in an outbred species, like man, they represent unique animal models of their respective human counterparts in which to determine the underlying immunologic defect(s), to evaluate novel approaches to immunotherapy or gene therapy, and to evaluate therapeutic regimens for opportunistic infections associated with SCID.

摘要

本综述描述了家畜中两种自然发生的严重联合免疫缺陷(SCID)模型的临床、免疫和病理特征,这些模型代表了人类SCID的不同形式。犬X连锁SCID(XSCID)具有X连锁隐性遗传模式,因此代表了美国最常见的人类SCID形式的模型。患病犬循环B细胞百分比正常,表型成熟但无功能的T细胞百分比低至正常。马的严重联合免疫缺陷是SCID的常染色体隐性形式,其特征是严重淋巴细胞减少,影响B细胞和T细胞系,最可能是由于淋巴干细胞缺陷。由于这些疾病在像人类一样的远交物种中自然发生,它们代表了各自人类对应疾病的独特动物模型,可用于确定潜在的免疫缺陷,评估免疫疗法或基因疗法的新方法,以及评估与SCID相关的机会性感染的治疗方案。

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