The effects of cyclophosphamide on the toxicity and immunogenicity of ricin A chain immunotoxin in rats.

Molecular biotherapy Pub Date : 1990-09-01
J B Stoudemire, R Mischak, C Foxall, W S Harkonen, M Del Rio, L E Spitler
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Abstract

We conducted a study to determine if treatment with cyclophosphamide (CY) could suppress the formation of anti-murine and anti-ricin A chain antibodies in rats treated with a murine monoclonal antibody-ricin A chain immunotoxin (IT). Female Sprague-Dawley rats received intravenous doses of IT at a dose of 5 mg/kg body weight alone or in combination with CY at a dose level of either 10 or 20 mg/kg body weight. The IT was given as one or two courses consisting of five consecutive daily intravenous injections (days 0 to 4, or days 0 to 4 and days 21 to 25 of the study). Cyclophosphamide was given on days 2, 4, 6, 13, and 17 of the study to the group receiving a single course of IT; additional doses of CY were administered on days 23, 25, and 27 to the group receiving two courses of IT. On days 4, 14, 21, 28, and 35, animals from each group were evaluated for antibodies to murine IgG and ricin A chain, and for clinical laboratory parameters and histopathology. Animals receiving IT alone developed significant titers of both anti-murine and anti-ricin A chain antibodies. Compared with the response in the animals receiving single-course IT, the response to both of the components of the IT was significantly increased on days 28 and 35 in the animals receiving a second course of IT. The groups receiving a combination of either one or two courses of CY and IT demonstrated a significantly decreased antibody response to both the murine IgG and the ricin A chain compared with the group receiving IT alone.(ABSTRACT TRUNCATED AT 250 WORDS)

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环磷酰胺对蓖麻毒素A链免疫毒素大鼠毒性及免疫原性的影响。
我们进行了一项研究,以确定环磷酰胺(CY)治疗是否可以抑制小鼠单克隆抗体-蓖麻毒素a链免疫毒素(IT)治疗的大鼠抗小鼠和抗蓖麻毒素a链抗体的形成。雌性Sprague-Dawley大鼠单独静脉注射剂量为5 mg/kg体重的IT,或与10或20 mg/kg体重的CY联合注射。IT作为一个或两个疗程给予,包括连续5次每日静脉注射(研究的第0至4天,或第0至4天和第21至25天)。在研究的第2天、第4天、第6天、第13天和第17天给予单疗程IT组环磷酰胺;在第23、25、27天对接受两个疗程IT的组给予额外剂量的CY。在第4、14、21、28和35天,对各组动物进行小鼠IgG和蓖麻毒素A链抗体检测,并检测临床实验室参数和组织病理学。单独接受IT治疗的动物产生了显著的抗小鼠和抗蓖麻毒素A链抗体滴度。与接受单疗程信息技术的动物相比,接受第二疗程信息技术的动物在第28天和第35天对信息技术两部分的反应都显著增加。与单独接受IT的组相比,接受一个或两个疗程CY和IT联合治疗的组对小鼠IgG和蓖麻毒素a链的抗体反应明显降低。(摘要删节250字)
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