DEFECTIVE CALCIUM-DEPENDENT SIGNAL-TRANSDUCTION IN T-LYMPHOCYTES OF ATAXIA-TELANGIECTASIA

被引:32
作者
KONDO, N
INOUE, R
NISHIMURA, S
KASAHARA, K
KAMEYAMA, T
MIWA, Y
LORENZO, PR
ORII, T
机构
[1] Department of Pediatrics, Gifu University School of Medicine, Gifu
关键词
D O I
10.1111/j.1365-3083.1993.tb01692.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T-cell functions of two patients with ataxia-telangiectasia were investigated. Patients with ataxia-telangiectasia had reduced percentages of circulating CD3+ cells and CD4+ cells, although neither patient had a reduced percentage of circulating CD8+ cells. The proliferative responses and interleukin-2 production of peripheral blood mononuclear cells to T-cell mitogens were reduced in the patients. The intracellular calcium concentration in T cells or CD4+ cells from both patients was only slightly increased after phytohaemagglutinin stimulation. Moreover, the concentration after OKT3 stimulation was not or only slightly increased in T cells or CD4+ cells from both patients. Our results suggest that the functional defect of T cells is caused by defective Ca2+-dependent signal transduction through the CD3 complex of the surface in T cells of ataxia-telangiectasia.
引用
收藏
页码:45 / 48
页数:4
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