Groh V, Porcelli S, Fabbi M, Lanier L L, Picker L J, Anderson T, Warnke R A, Bhan A K, Strominger J L, Brenner M B
Department of Biochemistry and Molecular Biology, Harvard University, Cambridge, Massachusetts 02138.
J Exp Med. 1989 Apr 1;169(4):1277-94. doi: 10.1084/jem.169.4.1277.
A direct quantitative and phenotypic cytofluorographic analysis of TCR-gamma/delta+ lymphocytes as well as an immunohistologic study of their tissue distribution and microanatomy was made possible by the availability of two mAbs (anti-TCR-delta 1 and anti-C gamma M1) specific for framework determinants on human TCR gamma and delta chains, respectively. TCR-gamma/delta+ lymphocytes, ranging between greater than 0.5 and 16% of CD3+ cells, were found in fetal and postnatal thymus, fetal and adult peripheral lymphoid organs, and adult peripheral blood. While TCR-gamma/delta+ lymphocytes comprised a small subpopulation of T cells (mean, approximately 4%) occasionally greater than 10-16% of CD3+ cells expressed TCR-gamma/delta. Virtually all TCR-gamma/delta+ thymocytes/lymphocytes expressed CD7, CD2, and CD5 but were heterogeneous with respect to their expression of CD1, CD4, CD8, CD28, CD11b, CD16, and Leu-7. Human TCR-gamma/delta+ cells populate both organized lymphoid tissues (thymus, tonsil, lymphnode, and spleen) as well as the gut- and skin-associated lymphoid systems at similar frequencies without obvious tropism for epithelial microenvironments. TCR-gamma/delta+ lymphocytes tend to be located within a given organ wherever TCR-alpha/beta+ lymphocytes are found. This study shows that TCR-gamma/delta+ lymphocytes constitute a small but numerically important, phenotypically diverse T cell population distributed throughout the body. These results support the concept that TCR-gamma/delta+ cells comprise a distinct, functionally heterogeneous, mature T cell sublineage that may substantially broaden the T cell repertoire at all immunologically relevant sites.
两种分别针对人TCRγ和δ链构架决定簇的单克隆抗体(抗-TCRδ1和抗-CγM1)的问世,使得对TCRγ/δ+淋巴细胞进行直接的定量和表型细胞荧光分析以及对其组织分布和显微解剖学进行免疫组织学研究成为可能。在胎儿和出生后的胸腺、胎儿和成人的外周淋巴器官以及成人外周血中发现,TCRγ/δ+淋巴细胞占CD3+细胞的比例在大于0.5%至16%之间。虽然TCRγ/δ+淋巴细胞构成了T细胞的一个小亚群(平均约为4%),但偶尔有超过10% - 16%的CD3+细胞表达TCRγ/δ。几乎所有的TCRγ/δ+胸腺细胞/淋巴细胞都表达CD7、CD2和CD5,但在CD1、CD4、CD8、CD28、CD11b、CD16和Leu - 7的表达方面存在异质性。人类TCRγ/δ+细胞以相似的频率分布于有组织的淋巴组织(胸腺、扁桃体、淋巴结和脾脏)以及肠道和皮肤相关淋巴系统中,对上皮微环境没有明显的趋向性。无论在哪里发现TCRα/β+淋巴细胞,TCRγ/δ+淋巴细胞往往都位于给定器官内。这项研究表明,TCRγ/δ+淋巴细胞构成了一个数量虽少但在数值上很重要、表型多样的T细胞群体,分布于全身。这些结果支持了这样一种概念,即TCRγ/δ+细胞构成了一个独特的、功能异质性的成熟T细胞亚系,可能在所有免疫相关部位显著拓宽T细胞库。