Leukocyte adhesion deficiency: molecular basis and functional consequences.

Immunodeficiency reviews Pub Date : 1988-01-01
A Fischer, B Lisowska-Grospierre, D C Anderson, T A Springer
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引用次数: 0

Abstract

Leukocyte adhesion deficiency disease is characterized by a mutation in the gene encoding the beta-subunit shared by three adhesive heterodimers, LFA-1, Mac-1 (CR3) and p150,95 expressed by leukocytes. An absent or abnormal beta-subunit leads to defective expression of the three heterodimers. Severe and moderate phenotypes of the disease are defined by absent and low surface expression of the adhesion molecules. The disease causes an inability of phagocytic cells to adhere to endothelial cells and thereafter to migrate to sites of infections. Severe widespread life-threatening bacterial and fungal infections are the consequences of this abnormality. Cure of the disease can be effected by allogeneic bone marrow transplantation. T-lymphocyte adhesion to various cells is also impaired; its consequences are, however, limited because of the existence of other T-cell-adhesive pathways. Nevertheless, haploidentical bone marrow graft rejection does not occur in the severe phenotype, an indication for possible immunotherapy with LFA-1 specific monoclonal antibodies.

白细胞粘附缺陷:分子基础和功能后果。
白细胞粘附缺乏症的特征是编码三种粘附异二聚体LFA-1、Mac-1 (CR3)和p150,95共享的β亚基的基因突变。缺失或异常的β亚基导致三种异源二聚体的表达缺陷。该疾病的严重和中度表型由黏附分子的缺失和低表面表达来定义。这种疾病导致吞噬细胞不能附着在内皮细胞上,然后迁移到感染部位。严重的、广泛的、危及生命的细菌和真菌感染是这种异常的后果。同种异体骨髓移植可以治愈这种疾病。t淋巴细胞对各种细胞的粘附也受损;然而,由于存在其他t细胞粘附途径,其结果是有限的。然而,单倍体骨髓移植排斥反应在严重表型中不会发生,这表明可能使用LFA-1特异性单克隆抗体进行免疫治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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