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促红细胞生成素模拟物-IgG4融合蛋白CNTO 530对大鼠和家兔胚胎-胎儿发育的影响。

Effects of CNTO 530, an erythropoietin mimetic-IgG4 fusion protein, on embryofetal development in rats and rabbits.

作者信息

Martin Pauline L, Sachs Clifford, Hoberman Alan, Jiao Qun, Bugelski Peter J

机构信息

Centocor Research and Development, Inc., Radnor, Pennsylvania, USA.

出版信息

Birth Defects Res B Dev Reprod Toxicol. 2010 Apr;89(2):87-96. doi: 10.1002/bdrb.20227.

Abstract

BACKGROUND

CNTO 530is a biopharmaceutical consisting of a novel peptide that mimics the actions of erythropoietin, fused to the Fc fragment of human IgG4. Pharmacokinetic and pharmacodynamic studies showed that CNTO 530 produced sustained increases in red blood cell parameters in rats and rabbits and that the serum half life of CNTO 530 was 2 days in rabbits and 3 days in rats.

METHODS

For the evaluation of embryofetal development, CNTO 530 was injected at loading doses of 0, 0.9/1, 6, or 60 mg/kg subcutaneously (SC) on gestation day (GD)7 followed by maintenance doses of 0, 0.3, 2, or 20 mg/kg SC every 3 days through GD16 in rats and every 2 days through GD19 in rabbits (GD0 was the day of mating). Rats were Caesarean sectioned on GD21, rabbits on GD29.

RESULTS

Administration of CNTO 530 was associated with an increase in hematocrit at all dose levels and a decrease in maternal body weight gains. Fetuses exhibited reduced body weight and delayed ossification. Soft tissue changes were limited to cardiovascular alterations in the high-dose rabbits only. Rat and rabbit fetuses were exposed to CNTO 530 in all dose groups.

CONCLUSIONS

These studies show that the embryo/fetal development effects observed following CNTO 530 treatment during organogenesis are qualitatively similar to those seen with other erythropoietin agonists and are likely a secondary consequence of increased hematocrit in the dams. Unlike other erythropoietin receptor agonists, CNTO 530 was able to cross the placental barrier, which was considered likely the result of FcRn-mediated transcytosis.

摘要

背景

CNTO 530是一种生物制药产品,由一种模拟促红细胞生成素作用的新型肽与人类IgG4的Fc片段融合而成。药代动力学和药效学研究表明,CNTO 530可使大鼠和兔子的红细胞参数持续增加,且CNTO 530在兔子体内的血清半衰期为2天,在大鼠体内为3天。

方法

为评估胚胎胎儿发育情况,在妊娠第7天,对大鼠皮下注射剂量分别为0、0.9/1、6或60mg/kg的负荷剂量CNTO 530,随后在妊娠第16天前每3天皮下注射维持剂量0、0.3、2或20mg/kg;对兔子在妊娠第7天皮下注射剂量分别为0、0.9/1、6或60mg/kg的负荷剂量CNTO 530,随后在妊娠第19天前每2天皮下注射维持剂量0、0.3、2或20mg/kg(妊娠第0天为交配日)。大鼠在妊娠第21天剖宫产,兔子在妊娠第29天剖宫产。

结果

在所有剂量水平下,给予CNTO 530均导致血细胞比容升高和母体体重增加减少。胎儿体重减轻,骨化延迟。软组织变化仅限于高剂量组兔子的心血管改变。所有剂量组的大鼠和兔子胎儿均接触到了CNTO 530。

结论

这些研究表明,在器官形成期用CNTO 530治疗后观察到的胚胎/胎儿发育影响在性质上与其他促红细胞生成素激动剂所见相似,可能是母鼠血细胞比容升高的继发结果。与其他促红细胞生成素受体激动剂不同,CNTO 530能够穿过胎盘屏障,这被认为可能是FcRn介导的转胞吞作用的结果。

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