DiSanto J P, Keever C A, Small T N, Nicols G L, O'Reilly R J, Flomenberg N
Effector Lymphocyte Biology, Laboratory Sloan-Kettering Institute for Cancer Research, New York, New York 10021.
J Exp Med. 1990 May 1;171(5):1697-704. doi: 10.1084/jem.171.5.1697.
We have characterized a child with a severe combined immunodeficiency disease syndrome with increased numbers, but a normal distribution, of CD3+ T cells. This patient's immunological defect appears to be attributable to a selective deficiency in T cell production of IL-2, which may reflect a subtle abnormality in the IL-2 gene locus or a defect in a regulatory factor necessary for IL-2 transcription. The increased numbers of phenotypically normal T cells in this patient suggest that alternative pathways of T cell development exist in man or that IL-2 production intra- and extrathymically is controlled via distinct regulatory mechanisms.
我们已对一名患有严重联合免疫缺陷病综合征的儿童进行了特征描述,该患儿CD3 + T细胞数量增加,但分布正常。该患者的免疫缺陷似乎归因于T细胞产生白细胞介素-2(IL-2)的选择性缺陷,这可能反映了IL-2基因位点的细微异常或IL-2转录所需调节因子的缺陷。该患者表型正常的T细胞数量增加表明,人类存在T细胞发育的替代途径,或者胸腺内和胸腺外IL-2的产生是通过不同的调节机制控制的。