Sobotková E, Sůla K, Nouza K
Institute of Experimental Medicine, Czechoslovak Academy of Sciences, Prague.
Neoplasma. 1988;35(4):361-7.
Using the model of Sarcoma I (SaI) (H-2a) tumor allograft transplanted to normal B10 (H-2b) mice and to B10 mice pretreated with ATS, we studied the effects of anti-Thy-1,2 monoclonal antibody (MTA) and compared them with those of rabbit polyvalent antiserum against mouse thymocytes (ATS). When administered shortly before tumor transplantation, MTA showed immunosuppressive effects, at one dose identical to those of ATS, at two doses exceeding ATS effects. In the period following the transplantation of SaI to normal mice, single doses of MTA and ATS showed weak antitumor effects. In mice immunosuppressed with ATS before the tumor transplantation the effects of each agent differed: MTA showed opposite immunomodulatory effects depending on the period of its administration, while ATS supported the primary growth of tumors independent of the time of administration. The results indicate that the immunomodulatory influence of MTA on the development of the tumor allograft is more selective than that of ATS.
利用移植到正常B10(H-2b)小鼠和经抗胸腺细胞血清(ATS)预处理的B10小鼠体内的肉瘤I(SaI)(H-2a)肿瘤同种异体移植模型,我们研究了抗Thy-1,2单克隆抗体(MTA)的作用,并将其与兔抗小鼠胸腺细胞多价抗血清(ATS)的作用进行比较。在肿瘤移植前不久给药时,MTA显示出免疫抑制作用,在一个剂量下与ATS相同,在两个剂量下超过ATS的作用。在将SaI移植到正常小鼠后的时期,单剂量的MTA和ATS显示出较弱的抗肿瘤作用。在肿瘤移植前用ATS免疫抑制的小鼠中,每种药物的作用有所不同:MTA根据其给药时期显示出相反的免疫调节作用,而ATS则支持肿瘤的原发性生长,与给药时间无关。结果表明,MTA对肿瘤同种异体移植发育的免疫调节影响比ATS更具选择性。