King D P, Strober S, Kaplan H S
J Immunol. 1981 Sep;127(3):1085-9.
BALB/c mice were treated with total lymphoid irradiation (TLI; 3400 rads) or single-dose, whole-body irradiation (WBI; 550 rads), and the lymph nodes and spleen were assayed for the level of H-2, Ia, Thy-1.2, Lyt-1.2, Lyt-2.2,3.2, and TL-bearing cells by an in vitro cytotoxicity assay. The level of cells bearing all these markers, except for TL, was similar to that observed in normal unirradiated mice. The level of TL+ cells was increased 10- to 20-fold in the TLI-treated mice as compared to WBI-treated mice or normals. The increased number of TL+ cells persisted for at lest 200 days after radiotherapy, and was not dependent upon irradiation of the thymus. However, thymectomy before TLI prevented the subsequent development of peripheral TL+ cells. The findings suggest that this abnormal subpopulation of T cells develops as a result of changes in the peripheral lymphoid tissue microenvironment induced by TLI.
用全身淋巴照射(TLI;3400拉德)或单剂量全身照射(WBI;550拉德)处理BALB/c小鼠,通过体外细胞毒性试验检测淋巴结和脾脏中携带H-2、Ia、Thy-1.2、Lyt-1.2、Lyt-2.2、3.2和TL的细胞水平。除TL外,所有这些标志物的细胞水平与未照射的正常小鼠中观察到的相似。与WBI处理的小鼠或正常小鼠相比,TLI处理的小鼠中TL+细胞水平增加了10至20倍。放疗后,TL+细胞数量增加至少持续200天,且不依赖于胸腺照射。然而,TLI前进行胸腺切除术可阻止外周TL+细胞的后续发育。这些发现表明,这种异常的T细胞亚群是由TLI诱导的外周淋巴组织微环境变化导致的。