Pisarev V M, Smirnova N N, Pevnitskiĭ L A
Biull Eksp Biol Med. 1977 Sep;84(9):327-30.
Administration of cyclophosphamide in a dose of 50 to 400 mg/kg to mice immunized with sheep red blood cells failed to decrease significantly the capacity of the splenic cells of these mice to suppress the primary immune response in transplantation to intact syngeneic recipients. Irradiation of the donors of immune splenic cells (ISC) in a dose of 900 r or treatment of ISC in vitro with mitomycin C failed to influence their suppressor activity. Supernatant obtained after the ultracentrifugation of ISC treated with ultrasound inhibited the primary immune response of intact mice. A conclusion was drawn that the suppressor effect of ISC was caused by the factor produced by T-cells. Active proliferation of these cells was not necessary for the realization of its action.
给用绵羊红细胞免疫的小鼠注射剂量为50至400毫克/千克的环磷酰胺,未能显著降低这些小鼠脾细胞抑制移植到同基因正常受体时的初次免疫反应的能力。用900拉德剂量照射免疫脾细胞(ISC)供体或在体外用丝裂霉素C处理ISC,均未影响其抑制活性。超声处理过的ISC超速离心后获得的上清液抑制了正常小鼠的初次免疫反应。得出的结论是,ISC的抑制作用是由T细胞产生的因子引起的。这些细胞的活跃增殖对于其作用的实现并非必要。