Maki T, Satomi S, Gotoh M, Monaco A P
J Immunol. 1986 May 1;136(9):3298-303.
Suppressive activity of culture supernatant of AS-9 (AS-9 CS), a T cell hybridoma line that was derived from fusion of BW5147 thymoma and splenic T cells of anti-lymphocyte serum-treated C3H mice, was analyzed. AS-9 CS inhibited allogeneic cytotoxic T lymphocyte (CTL) generation as well as T cell proliferation to alloantigens and mitogens, but failed to inhibit B cell response to lipopolysaccharide or growth of tumor and fibroblast cells. Although addition of AS-9 CS to the allogeneic sensitization culture as late as on day 2 of incubation resulted in maximal inhibiton of CTL generation, removal of AS-9 CS on day 3 of incubation abolished its inhibitory effect. Addition of purified IL 2 together with AS-9 CS to the allogeneic sensitization cultures only partially abrogated the suppression. Experiments with IL 2-dependent cytotoxic T cell line (CTLL) showed that AS-9 CS suppressed the IL 2-induced proliferation of CTLL. Preincubation of AS-9 CS with CTLL removed its inhibitory effect on CTL generation. These results indicate that AS-9 CS interferes with the mechanism of T cell activation by IL 2. On this basis, AS-9 CS was named contra-IL 2.
对AS-9(AS-9培养上清液)的抑制活性进行了分析,AS-9是一种T细胞杂交瘤细胞系,由BW5147胸腺瘤与抗淋巴细胞血清处理的C3H小鼠的脾T细胞融合而成。AS-9培养上清液抑制同种异体细胞毒性T淋巴细胞(CTL)的产生以及T细胞对同种异体抗原和丝裂原的增殖,但不能抑制B细胞对脂多糖的反应或肿瘤细胞和成纤维细胞的生长。尽管在培养第2天很晚的时候向同种异体致敏培养物中添加AS-9培养上清液会导致CTL产生的最大抑制,但在培养第3天去除AS-9培养上清液会消除其抑制作用。将纯化的IL-2与AS-9培养上清液一起添加到同种异体致敏培养物中只能部分消除抑制作用。对依赖IL-2的细胞毒性T细胞系(CTLL)的实验表明,AS-9培养上清液抑制IL-2诱导的CTLL增殖。AS-9培养上清液与CTLL预孵育可消除其对CTL产生的抑制作用。这些结果表明,AS-9培养上清液干扰了IL-2激活T细胞的机制。在此基础上,AS-9培养上清液被命名为抗IL-2。