Bash J A, Waksman B H
J Immunol. 1975 Feb;114(2 pt 2):782-7.
DNA synthesis (3H-thymidine incorporation) of DA rat spleen and lymph node cells cultured with PHA or (DA x Lewis)F1 lymph node cells was profoundly inhibited by pretreatment with large i.v. doses of antigen (greater than 100 mg OA or greater than 10(10) SRBC) 24 hr before culture. This effect, seen as early as 3 to 6 hr after antigen administration, had disappeared within 7 days. Similar depressed spleen cell responses were seen 9 days after footpad injection of 200 mug OA in complete adjuvant. Lymph node responses showed a similar inhibition only in the presence of specific antigen in culture. In all experiments in which antigen administration resulted in decreased responses, removal of glass wool adherent cells restored responsiveness to normal. The failure of purified macrophages to reestablish inhibition favored the interpretation that an adherent suppressor cell distinct from the macrophage is activated by antigen in vivo to regulate T cell responses in vitro.
用PHA培养的DA大鼠脾细胞和淋巴结细胞或(DA×Lewis)F1淋巴结细胞的DNA合成(3H-胸腺嘧啶核苷掺入),在培养前24小时经静脉注射大剂量抗原(大于100mg OA或大于10¹⁰个SRBC)预处理后受到显著抑制。这种效应早在抗原给药后3至6小时就可见到,在7天内消失。在完全佐剂中足垫注射200μg OA 9天后,可见到类似的脾细胞反应受抑情况。淋巴结反应仅在培养中有特异性抗原存在时才表现出类似的抑制。在所有抗原给药导致反应降低的实验中,去除玻璃棉黏附细胞可使反应恢复正常。纯化的巨噬细胞不能重建抑制作用,这支持了一种解释,即体内抗原激活了一种不同于巨噬细胞的黏附性抑制细胞,以调节体外的T细胞反应。