Ishikura H, Matsuura A, Ishii Y, Natori T, Kikuchi K, Aizawa M
Clin Exp Immunol. 1985 Dec;62(3):570-8.
Distributions and ultrastructures of T cell subsets within grafts were studied in unmodified, first-set rat renal transplantation systems (F344----WKA, TO----WKA). Rejections took place within 9.0 +/- 0.5 and 12.2 +/- 1.6 days, respectively. Mouse monoclonal antibodies, R1-3B3 and R1-10B5, were used here for the detection of RLyt-1 and RLyt-2 antigenic systems of rat T cells, respectively. RLyt-1 and RLyt-2 antigens are chemical homologues of mouse Lyt-1 and Lyt-2,3 antigens. In the perivascular areas, RLyt-1+,2- cells were the predominant T cells in earlier stages of rejection. However, toward the end of rejection, RLyt-1+,2- cells decreased in number, with the increase in RLyt-1+,2+ cells. In the interstitial peritubular areas, RLyt-1+,2+ cells were the predominant T cells throughout the course of rejection. Thus, the major T cells in perivascular areas were helper T cells in earlier stages and cytotoxic/suppressor T cells in the later stage, whereas in interstitial peritubular areas, cytotoxic/suppressor T cells were the major T cell population during the entire course of rejection. Ultrastructural studies revealed that many RLyt-2+ blast cells had clustered dense bodies, and that RLyt-2+ cells were found among renal tubular epithelial cells. Renal tubular cells adjacent to RLyt-2+ cells were degenerative in most cases. In addition, membranous structures seen in grafts were RLyt-1+,2+,Ia-, suggesting that they might derive from the destruction of cytotoxic/suppressor T cells after several target cell lyses in vivo.
在未修饰的首次大鼠肾移植系统(F344→WKA,TO→WKA)中研究了移植物内T细胞亚群的分布和超微结构。排斥反应分别在9.0±0.5天和12.2±1.6天内发生。这里使用小鼠单克隆抗体R1-3B3和R1-10B5分别检测大鼠T细胞的RLyt-1和RLyt-2抗原系统。RLyt-1和RLyt-2抗原是小鼠Lyt-1和Lyt-2,3抗原的化学同源物。在血管周围区域,RLyt-1 +,2-细胞是排斥早期的主要T细胞。然而,在排斥末期,RLyt-1 +,2-细胞数量减少,而RLyt-1 +,2+细胞增加。在间质肾小管周围区域,RLyt-1 +,2+细胞在整个排斥过程中是主要的T细胞。因此,血管周围区域的主要T细胞在早期是辅助性T细胞,后期是细胞毒性/抑制性T细胞,而在间质肾小管周围区域,细胞毒性/抑制性T细胞是整个排斥过程中的主要T细胞群体。超微结构研究显示,许多RLyt-2 +母细胞有聚集的致密体,并且在肾小管上皮细胞中发现了RLyt-2 +细胞。在大多数情况下,与RLyt-2 +细胞相邻的肾小管细胞发生变性。此外,在移植物中看到的膜性结构是RLyt-1 +,2+,Ia-,表明它们可能源自体内几个靶细胞裂解后细胞毒性/抑制性T细胞的破坏。