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环磷酰胺处理的白血病细胞的免疫原性。

Immunogenicity of cyclophosphamide-treated leukaemia cells.

作者信息

Kawalec M, Jakóbisiak M, Skórski T, Kawiak J

出版信息

Folia Biol (Praha). 1982;28(5):334-43.

PMID:6816636
Abstract

The median survival time of DBA/2Wf or CD2F1 hybrid mice increased after administration of 10(3) cells of lymphoid leukaemia L 1210 when the recipient mice were injected earlier with L 1210 cells pretreated in vivo with cyclophosphamide. To achieve this effect, at least 10(5) cells treated with cyclophosphamide should be used per mouse. This effect was immunologically specific and could not be induced by L-1 cells treated with cyclophosphamide, and was transferable by means of splenocytes. Such immunoprophylaxis was efficient for at least 100 days. Attempts at immunoprevention by means of the same cells treated with mitomycin C or killed by osmotic shock were unsuccessful.

摘要

当受体小鼠预先注射经环磷酰胺体内预处理的L 1210细胞后,给予10³个淋巴白血病L 1210细胞,DBA/2Wf或CD2F1杂交小鼠的中位生存时间延长。为达到此效果,每只小鼠至少应使用10⁵个经环磷酰胺处理的细胞。这种效应具有免疫特异性,不能由经环磷酰胺处理的L - 1细胞诱导产生,并且可通过脾细胞转移。这种免疫预防至少可持续100天。通过丝裂霉素C处理或渗透休克杀死的相同细胞进行免疫预防的尝试未成功。

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