Jitsukawa S, Faure F, Lipinski M, Triebel F, Hercend T
Laboratoire d'Immunologie Cellulaire, Département de Biologie Clinique, Villejuif, France.
J Exp Med. 1987 Oct 1;166(4):1192-7. doi: 10.1084/jem.166.4.1192.
We have previously characterized a CD3+ T cell receptor (TCR) alpha/beta- human fetal cloned cell line, termed F6C7, which surface-expresses a CD3-associated gamma chain identified by anti-NKFi, an mAb with a restricted clonotypic reactivity. Here, we have produced an additional antibody, anti-Ti-gamma A, which recognizes a public epitope of the gamma molecule defined by anti-NKFi. Ti-gamma A is present on approximately 3% of circulating lymphocytes with a wide range (1-15%) among 30 healthy individuals tested. Two-color immunofluorescence experiments performed with anti-Ti-gamma A and BMA 031 mAb (a reagent specific for the TCR-alpha/beta receptor) showed that surface expression of Ti-alpha/beta and Ti-gamma A is mutually exclusive. Moreover, it was found that most Ti-gamma A+ cells are CD2+, CD3+, CD4-, CD5+, NKH1-, HLA class II-negative. In contrast, the expression of the CD8 molecule on these T lymphocytes appears to be variable from one individual to another. Finally, we found that Ti-gamma A+ cells represent a majority of peripheral lymphocytes that express CD3 proteins but not the TCR-alpha/beta heterodimer. The delineation of this unique lymphocyte subset should help further studies on the biology of cells with a CD3-associated gamma complex.
我们之前已鉴定出一种CD3⁺T细胞受体(TCR)α/β⁻人胎儿克隆细胞系,称为F6C7,其表面表达一种与CD3相关的γ链,该γ链可被抗NKFi识别,抗NKFi是一种具有受限克隆型反应性的单克隆抗体。在此,我们制备了另一种抗体,抗Ti-γA,它识别由抗NKFi定义的γ分子的一个公共表位。在接受检测的30名健康个体中,Ti-γA存在于约3%的循环淋巴细胞上,范围较广(1%-15%)。用抗Ti-γA和BMA 031单克隆抗体(一种针对TCR-α/β受体的特异性试剂)进行的双色免疫荧光实验表明,Ti-α/β和Ti-γA的表面表达相互排斥。此外,发现大多数Ti-γA⁺细胞是CD2⁺、CD3⁺、CD4⁻、CD5⁺、NKH1⁻、HLA II类阴性。相反,这些T淋巴细胞上CD8分子的表达在个体之间似乎有所不同。最后,我们发现Ti-γA⁺细胞占表达CD3蛋白但不表达TCR-α/β异二聚体的外周淋巴细胞的大多数。对这一独特淋巴细胞亚群的描述应有助于进一步研究具有与CD3相关γ复合体的细胞的生物学特性。