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伴有T细胞受体/CD3复合物低表达的免疫缺陷。对T淋巴细胞活化的影响。

Immunodeficiency with low expression of the T cell receptor/CD3 complex. Effect on T lymphocyte activation.

作者信息

Le Deist F, Thoenes G, Corado J, Lisowska-Grospierre B, Fischer A

机构信息

INSERUM U 132, Hôpital, Necker-Enfants Malades, Paris, France.

出版信息

Eur J Immunol. 1991 Jul;21(7):1641-7. doi: 10.1002/eji.1830210709.

Abstract

We report the consequences of low expression of the T cell receptor (TcR)/CD3 complex by T lymphocytes from a 4-year-old boy with a mild immunodeficiency. TcR/CD3 expression was found to be deficient on both resting and activated T cells, using both anti-CD3 and anti-TcR alpha/beta monoclonal antibodies. As shown by immunofluorescence and immunoprecipitation studies, residual expression (corresponding to about 10% of normal) was detectable on resting and activated TcR alpha/beta+ T cells. Other T cell membrane receptors were normally expressed. The functional consequences of this TcR/CD3 expression deficiency included an absence of T cell proliferation, interleukin 2 receptor expression and calcium flux following anti-CD3 and anti-CD2 antibody-triggered T cell activation. Antigen (tetanus toxoid, Candida and allogeneic cell)-induced proliferation was detectable. In contrast, cytotoxic T cell activity towards allogeneic cells was deficient. These findings shed light on the function of the TcR/CD3 complex and indicate that the expression of a limited number of TcR/CD3 receptors may be sufficient to trigger antigen-specific T cell activation (and, possibly, differentiation) and that anti-CD3 antibody-induced T cell activation differs somewhat from antigen/major histocompatibility complex molecule-induced activation. These results also confirm that the CD2 pathway of T cell activation is CD3 dependent.

摘要

我们报告了一名患有轻度免疫缺陷的4岁男孩的T淋巴细胞中T细胞受体(TcR)/CD3复合物低表达的后果。使用抗CD3和抗TcRα/β单克隆抗体发现,静息和活化的T细胞上的TcR/CD3表达均不足。免疫荧光和免疫沉淀研究表明,在静息和活化的TcRα/β+ T细胞上可检测到残留表达(约为正常水平的10%)。其他T细胞膜受体表达正常。这种TcR/CD3表达缺陷的功能后果包括抗CD3和抗CD2抗体触发T细胞活化后T细胞增殖、白细胞介素2受体表达和钙通量缺失。抗原(破伤风类毒素、念珠菌和异体细胞)诱导的增殖可检测到。相比之下,对异体细胞的细胞毒性T细胞活性不足。这些发现揭示了TcR/CD3复合物的功能,并表明有限数量的TcR/CD3受体的表达可能足以触发抗原特异性T细胞活化(以及可能的分化),并且抗CD3抗体诱导的T细胞活化与抗原/主要组织相容性复合体分子诱导的活化有所不同。这些结果还证实了T细胞活化的CD2途径是CD3依赖性的。

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