Greiner D L, Reynolds G W, Lubaroff D M
Thymus. 1982 Feb;4(2):77-90.
The T-lymphocyte differentiation alloantigens, A.R.T.-1 and A.R.T.-2 were used to follow the functional development of these cells in the rat. Delayed hypersensitivity and lymphocytes cytotoxic for allogeneic tumor cells were present in adoptively transferred recipients by 3 wk postirradiation and fetal liver reconstitution. However, these animals did not regain appreciable GvH potential until 7.5 wk postreconstitution. Normal percentages of A.R.T-1 lymphocytes were observed at all times in the spleen and lymph nodes of these animals, whereas, below normal numbers of A.R.T-2 lymphocytes were observed up to 7.5 wk postreconstitution. Depletion experiments using specific anti-A.R.T. sera demonstrated that the proliferative response to PHA and the cytotoxic lymphocyte response to alloantigens were reduced after treatment with anti-A.R.T.-1, but not with anti-A.R.T.-2. In contrast, the GvH potential of lymph node cells was reduced by treatment with either anti-A.R.T.-1 or anti-A.R.T.-2 serum plus complement. The use of these A.R.T. alloantisera in the rat has greatly facilitated the establishment of differentiation patterns for functional T lymphocytes and has resulted in the association of specific functional T-cell subpopulations with characteristic surface alloantigens.
利用T淋巴细胞分化同种异体抗原A.R.T.-1和A.R.T.-2来追踪大鼠体内这些细胞的功能发育。在接受过照射并经胎肝重建的受体动物中,在照射后3周时出现了迟发型超敏反应以及对同种异体肿瘤细胞具有细胞毒性的淋巴细胞。然而,这些动物直到重建后7.5周才恢复明显的移植物抗宿主(GvH)潜能。在这些动物的脾脏和淋巴结中,始终观察到A.R.T-1淋巴细胞的百分比正常,而在重建后长达7.5周的时间里,观察到A.R.T-2淋巴细胞的数量低于正常水平。使用特异性抗A.R.T.血清进行的清除实验表明,用抗A.R.T.-1处理后,对PHA的增殖反应以及对同种异体抗原的细胞毒性淋巴细胞反应降低,但用抗A.R.T.-2处理则不然。相反,用抗A.R.T.-1或抗A.R.T.-2血清加补体处理会降低淋巴结细胞的GvH潜能。在大鼠中使用这些A.R.T.同种异体抗血清极大地促进了功能性T淋巴细胞分化模式的建立,并导致特定功能性T细胞亚群与特征性表面同种异体抗原的关联。