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含外毒素修饰片段的新型抗HER2免疫毒素在BALB/C小鼠中的安全性评估

Evaluation of the Safety of A Novel Anti-HER2 Immunotoxin Containing Modified Fragment of Exotoxin in BALB/C Mice.

作者信息

Saadatkhah Fatemeh, Hajhashemi Valiollah, Naimi Azar, Akbari Vajihe, Kolahdoozan Melika

机构信息

Department of Pharmaceutical Biotechnology, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran.

Department of Pharmacology and Toxicology, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

Iran J Biotechnol. 2025 Apr 1;23(2):e4000. doi: 10.30498/ijb.2025.481960.4000. eCollection 2025 Apr.

Abstract

BACKGROUND

Human epidermal growth factor-2 (HER-2) receptors are overexpressed in some malignancies like breast cancer. Previously, we constructed a novel anti-HER immunotoxin, scFv-PE35KDEL, containing modified fragments of exotoxin, which showed remarkable cytotoxicity against breast cancer cells. safety evaluation is essential for evaluating toxicity to perform efficacy studies. This study aimed to evaluate the acute toxicity of scFv-PE35KDEL in BALB/c mice.

OBJECTIVES

The objective of this research was to express and purify the recombinant scFv-PE35KDEL protein and remove its endotoxin content, as well as to evaluate its toxicity profile by determining the LD and monitoring body weight changes in BALB/c mice following injection.

MATERIALS AND METHODS

After expression and purification of scFv-PE35KDEL, BALB/c mice were intraperitoneally administered single doses of 250, 500, 1000, and 2000 µg.kg of immunotoxin. Mice's weight, body temperature, and acute toxicity symptoms were evaluated every odd day for two weeks. Histopathological evaluation of the kidney, liver and lungs was performed.

RESULTS

All mice died after a single dose of 2000 µg.kg of immunotoxin, but after exposure to 1000 µg.mg, all mice survived for 15 days. There was no significant difference in the body temperature between the groups ( > 0.05). There was a considerable weight loss at 500 and 1000 µg.kg doses until three days ( < 0.05) which recovered gradually. Diarrhea and loss of muscular tonicity were among the common adverse effects, which were worsened by increasing the dose to 1000 µg.mg. Based on histopathological analysis, no specific toxicity was observed in the liver and kidney tissues at doses up to 1000 µg.kg.

CONCLUSION

These findings revealed that the LD50 of scFv-PE35KDEL is in the range of 1000-2000 µg.mg and it seems to be a safe and non-toxic agent, and could be a promising candidate for anti-HER2 cancer therapy. However, further evaluations are required.

摘要

背景

人表皮生长因子-2(HER-2)受体在某些恶性肿瘤如乳腺癌中过度表达。此前,我们构建了一种新型抗HER免疫毒素scFv-PE35KDEL,其包含外毒素的修饰片段,对乳腺癌细胞显示出显著的细胞毒性。安全性评估对于评估毒性以进行疗效研究至关重要。本研究旨在评估scFv-PE35KDEL在BALB/c小鼠中的急性毒性。

目的

本研究的目的是表达和纯化重组scFv-PE35KDEL蛋白并去除其内毒素含量,以及通过测定半数致死量(LD)和监测BALB/c小鼠注射后体重变化来评估其毒性特征。

材料与方法

scFv-PE35KDEL表达纯化后,给BALB/c小鼠腹腔注射单剂量250、500、1000和2000μg/kg的免疫毒素。每隔一天评估小鼠体重、体温和急性毒性症状,持续两周。对肾脏、肝脏和肺进行组织病理学评估。

结果

单次注射2000μg/kg免疫毒素后所有小鼠死亡,但暴露于1000μg/kg后,所有小鼠存活了15天。各组间体温无显著差异(P>0.05)。500和1000μg/kg剂量组在三天内体重显著下降(P<0.05),随后逐渐恢复。腹泻和肌肉张力丧失是常见的不良反应,剂量增加到1000μg/kg时症状加重。基于组织病理学分析,在高达1000μg/kg的剂量下,肝脏和肾脏组织未观察到特异性毒性。

结论

这些结果表明,scFv-PE35KDEL的半数致死量在1000 - 2000μg/kg范围内,似乎是一种安全无毒的药物,可能是抗HER2癌症治疗的有前途的候选药物。然而,还需要进一步评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b060/12374125/e7d4d06ec338/IJB-23-2-e4000-g001.jpg

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