Petrov R V, Manyko V M, Khaitov R M, Seslavina L S
J Exp Med. 1971 Mar 1;133(3):640-8. doi: 10.1084/jem.133.3.640.
Sublethally (600 R) irradiated (CBA x C57BL)F(1) mice were grafted intravenously with parental lymph node cells in doses ranging from 0.2 x 10(6) to 12 x 10(6). The transplantation of these lymphoid cells leads to inactivation of the recipient's endogenous CFU (as measured by the diminution of the number of colonies registered on the 10th day after irradiation). A 50% inactivation was observed when the graft size of the CBA cells was 0.52 x 10(6). This figure for C57BL cells was 10 times more. This experimental system evaluates two simultaneously developing processes: the multiplication of endogenous CFU and the homograft reaction of transplanted lymphocytes against them. Both processes can be quantitatively estimated simultaneously in the same experiment by the determination of the number of colonies in corresponding experimental groups. Thus it was possible in a single experiment to compare quantitatively the effect of immunosuppressants on two points: (a) mitostatic action (suppression of CFU) and (b) lymphotoxic action. The latter, a true immunosuppressive effect, represents suppression of GVH activity of lymphoid cells and is demonstrated by abolition of the inhibition of endogenous colony formation. In the present system we have tested 6-MP, ALS, cyclophosphamide, hydrocortisone, and other drugs. The definite mitostatic and lymphotoxic doses of drugs are ascertained. Cyclophosphamide and ALS proved to be drugs with high dose ranges of selective lymphotoxic action. Hydrocortisone acetate had a more narrow range of selective lymphotoxic effect. 6-MP and Imuran (azathioprine) failed to exert any selective action on lymphoid elements. They possessed pronounced mitostatic efficiency, however.
用亚致死剂量(600拉德)照射(CBA×C57BL)F1代小鼠,然后静脉内移植亲本淋巴结细胞,移植剂量范围为0.2×10⁶至12×10⁶。这些淋巴细胞的移植导致受体内源性CFU失活(通过照射后第10天记录的集落数量减少来衡量)。当CBA细胞的移植量为0.52×10⁶时,观察到50%的失活。C57BL细胞的这一数值要高10倍。该实验系统评估两个同时发生的过程:内源性CFU的增殖以及移植淋巴细胞对它们的同种移植反应。在同一实验中,通过测定相应实验组中的集落数量,可以同时对这两个过程进行定量估计。因此,在单个实验中就有可能在两个方面定量比较免疫抑制剂的作用:(a)有丝分裂抑制作用(对CFU的抑制)和(b)淋巴细胞毒性作用。后者是一种真正的免疫抑制作用,表现为淋巴细胞GVH活性的抑制,并通过内源性集落形成抑制的消除来证明。在本系统中,我们测试了6 - MP、抗淋巴细胞血清(ALS)、环磷酰胺、氢化可的松及其他药物。确定了药物的明确有丝分裂抑制和淋巴细胞毒性剂量。环磷酰胺和ALS被证明是具有高剂量范围选择性淋巴细胞毒性作用的药物。醋酸氢化可的松的选择性淋巴细胞毒性作用范围较窄。6 - MP和硫唑嘌呤对淋巴细胞成分没有任何选择性作用。然而,它们具有明显的有丝分裂抑制效率。