Taylor N, Bacon K B, Smith S, Jahn T, Kadlecek T A, Uribe L, Kohn D B, Gelfand E W, Weiss A, Weinberg K
Division of Research Immunology and Bone Marrow Transplantation, Children's Hospital, Los Angeles, California 90027, USA.
J Exp Med. 1996 Nov 1;184(5):2031-6. doi: 10.1084/jem.184.5.2031.
A variant of severe combined immunodeficiency syndrome (SCID) with a selective inability to produce CD8 single positive T cells and a signal transduction defect in peripheral CD4+ cells has recently been shown to be the result of mutations in the ZAP-70 gene. T cell receptor (TCR) signaling requires the association of the ZAP-70 protein tyrosine kinase with the TCR complex. Human T cell leukemia virus type I-transformed CD4+ T cell lines were established from ZAP-70-deficient patients and normal controls. ZAP-70 was expressed and appropriately phosphorylated in normal T cell lines after TCR engagement, but was not detected in T cell lines from ZAP-70-deficient patients. To determine whether signaling could be reconstituted, wild-type ZAP-70 was introduced into deficient cells with a ZAP-70 retroviral vector. High titer producer clones expressing ZAP-70 were generated in the Gibbon ape leukemia virus packaging line PG13. After transduction, ZAP-70 was detected at levels equivalent to those observed in normal cells, and was appropriately phosphorylated on tyrosine after receptor engagement. The kinase activity of ZAP-70 in the reconstituted cells was also appropriately upregulated by receptor aggregation. Moreover, normal and transduced cells, but not ZAP-70-deficient cells, were able to mobilize calcium after receptor ligation, indicating that proximal TCR signaling was reconstituted. These results indicate that this form of SCID may be corrected by gene therapy.
最近研究表明,一种严重联合免疫缺陷综合征(SCID)变体,其特征为选择性无法产生CD8单阳性T细胞以及外周CD4 +细胞存在信号转导缺陷,是由ZAP - 70基因突变所致。T细胞受体(TCR)信号传导需要ZAP - 70蛋白酪氨酸激酶与TCR复合物结合。从ZAP - 70缺陷患者和正常对照中建立了人T细胞白血病病毒I型转化的CD4 + T细胞系。TCR激活后,正常T细胞系中可表达并适当磷酸化ZAP - 70,但在ZAP - 70缺陷患者的T细胞系中未检测到。为了确定信号传导是否可以重建,使用ZAP - 70逆转录病毒载体将野生型ZAP - 70导入缺陷细胞。在长臂猿白血病病毒包装细胞系PG13中产生了表达ZAP - 70的高滴度生产克隆。转导后,检测到的ZAP - 70水平与正常细胞中观察到的水平相当,并且受体激活后酪氨酸被适当磷酸化。重建细胞中ZAP - 70的激酶活性也通过受体聚集而适当上调。此外,正常细胞和转导细胞,而非ZAP - 70缺陷细胞,在受体连接后能够动员钙离子,表明近端TCR信号传导得以重建。这些结果表明,这种形式的SCID可能通过基因治疗得到纠正。