• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

VB6-845 的临床前评估:一种具有降低免疫原性潜力的抗 EpCAM 免疫毒素。

Preclinical evaluation of VB6-845: an anti-EpCAM immunotoxin with reduced immunogenic potential.

机构信息

Department of Research, Viventia Biotechnologies, Inc., Winnipeg, Manitoba, Canada.

出版信息

Cancer Biother Radiopharm. 2012 Nov;27(9):582-92. doi: 10.1089/cbr.2012.1200.271. Epub 2012 Aug 2.

DOI:10.1089/cbr.2012.1200.271
PMID:22856424
Abstract

VB6-845 is a recombinant immunotoxin comprised of deBouganin (a de-immunized plant toxin) genetically linked to an epithelial cell adhesion molecule (EpCAM)-targeting humanized Fab fragment (4D5MOCB). EpCAM is highly expressed on a wide range of epithelial tumors but has limited expression on most normal epithelia and therefore represents an excellent target for immunotherapy. A comprehensive preclinical evaluation was performed to determine the safety and suitability of VB6-845 as a systemically administered drug for the treatment of solid tumors. Efficacy studies in mice demonstrated that VB6-845 specifically and potently targeted EpCAM-positive tumors. In a dose-ranging study in Sprague-Dawley rats, single doses of VB6-845 were well-tolerated resulting in a no-observable adverse effect level (NOAEL) of 100 mg/kg whereas repeated doses of VB6-845 resulted in vascular leak-associated symptoms particularly at higher dose levels. However, much higher doses in Cynomolgus monkeys were well-tolerated when given as a 3-hour infusion mimicking the intended route of administration in the clinic. In addition, VB6-845 proved to be minimally immunogenic in monkeys. The toxicological data obtained in Cynomolgus monkeys indicated an excellent safety profile with a NOAEL value of 30 mg/kg (equivalent to a 10 mg/kg dose in humans). These results are supportive of an exploratory Phase I trial.

摘要

VB6-845 是一种重组免疫毒素,由去免疫植物毒素 deBouganin 与靶向上皮细胞黏附分子 (EpCAM) 的人源化 Fab 片段 (4D5MOCB) 通过基因连接而成。EpCAM 在广泛的上皮肿瘤中高度表达,但在上皮组织中表达有限,因此是免疫治疗的理想靶点。我们进行了全面的临床前评估,以确定 VB6-845 作为治疗实体瘤的全身性药物的安全性和适用性。在小鼠的疗效研究中,VB6-845 特异性地靶向 EpCAM 阳性肿瘤,并具有强大的疗效。在 Sprague-Dawley 大鼠的剂量范围研究中,VB6-845 的单剂量耐受良好,导致 100mg/kg 的无观察不良效应水平 (NOAEL),而 VB6-845 的重复剂量导致与血管渗漏相关的症状,特别是在较高剂量水平。然而,当在恒河猴中以模拟临床给药途径的 3 小时输注给予更高剂量时,恒河猴耐受良好。此外,VB6-845 在猴子中表现出最小的免疫原性。在恒河猴中获得的毒理学数据表明具有极好的安全性,NOAEL 值为 30mg/kg(相当于人类 10mg/kg 剂量)。这些结果支持探索性 I 期试验。

相似文献

1
Preclinical evaluation of VB6-845: an anti-EpCAM immunotoxin with reduced immunogenic potential.VB6-845 的临床前评估:一种具有降低免疫原性潜力的抗 EpCAM 免疫毒素。
Cancer Biother Radiopharm. 2012 Nov;27(9):582-92. doi: 10.1089/cbr.2012.1200.271. Epub 2012 Aug 2.
2
Engineering and biological characterization of VB6-845, an anti-EpCAM immunotoxin containing a T-cell epitope-depleted variant of the plant toxin bouganin.VB6-845的工程学与生物学特性,一种抗上皮细胞黏附分子免疫毒素,其包含植物毒素布干菌素的T细胞表位缺失变体
J Immunother. 2009 Jul-Aug;32(6):574-84. doi: 10.1097/CJI.0b013e3181a6981c.
3
Preclinical assessment of an anti-EpCAM immunotoxin: locoregional delivery provides a safer alternative to systemic administration.一种抗上皮细胞黏附分子免疫毒素的临床前评估:局部给药为全身给药提供了更安全的替代方案。
Cancer Biother Radiopharm. 2009 Aug;24(4):477-87. doi: 10.1089/cbr.2008.0579.
4
Granzyme B-based cytolytic fusion protein targeting EpCAM specifically kills triple negative breast cancer cells in vitro and inhibits tumor growth in a subcutaneous mouse tumor model.基于 granzyme B 的细胞溶素融合蛋白特异性靶向 EpCAM,可在体外杀伤三阴性乳腺癌细胞,并在皮下荷瘤小鼠模型中抑制肿瘤生长。
Cancer Lett. 2016 Mar 28;372(2):201-9. doi: 10.1016/j.canlet.2016.01.027. Epub 2016 Jan 21.
5
Increasing anticarcinoma activity of an anti-erbB2 recombinant immunotoxin by the addition of an anti-EpCAM sFv.通过添加抗EpCAM单链抗体片段增强抗erbB2重组免疫毒素的抗癌活性。
Clin Cancer Res. 2007 May 15;13(10):3058-67. doi: 10.1158/1078-0432.CCR-06-2454.
6
Therapeutic potential of amanitin-conjugated anti-epithelial cell adhesion molecule monoclonal antibody against pancreatic carcinoma.鹅膏蕈碱偶联抗上皮细胞黏附分子单克隆抗体对胰腺癌的治疗潜力。
J Natl Cancer Inst. 2012 Apr 18;104(8):622-34. doi: 10.1093/jnci/djs140. Epub 2012 Mar 27.
7
Construction, expression, and characterization of a recombinant immunotoxin targeting EpCAM.靶向上皮细胞黏附分子(EpCAM)的重组免疫毒素的构建、表达及特性分析
Mediators Inflamm. 2015;2015:460264. doi: 10.1155/2015/460264. Epub 2015 Apr 16.
8
EpCAM-specific vaccine response by modified antigen and chimeric costimulatory molecule in cynomolgus monkeys.食蟹猴中经修饰抗原和嵌合共刺激分子产生的EpCAM特异性疫苗反应。
J Immunother. 2008 Sep;31(7):644-55. doi: 10.1097/CJI.0b013e3181826d89.
9
Phase I trial of EpCAM-targeting immunotoxin MOC31PE, alone and in combination with cyclosporin.靶向EpCAM免疫毒素MOC31PE单药及联合环孢素的I期试验。
Br J Cancer. 2015 Dec 1;113(11):1548-55. doi: 10.1038/bjc.2015.380. Epub 2015 Nov 10.
10
A Novel Immunotoxin Targeting Epithelial Cell Adhesion Molecule Using Single Domain Antibody Fused to Diphtheria Toxin.一种使用与白喉毒素融合的单域抗体靶向上皮细胞粘附分子的新型免疫毒素。
Mol Biotechnol. 2023 Apr;65(4):637-644. doi: 10.1007/s12033-022-00565-2. Epub 2022 Sep 21.

引用本文的文献

1
Prediction of immunogenicity for humanized and full human therapeutic antibodies.预测人源化和全人源治疗性抗体的免疫原性。
PLoS One. 2020 Aug 31;15(8):e0238150. doi: 10.1371/journal.pone.0238150. eCollection 2020.
2
Bouganin, an Attractive Weapon for Immunotoxins.布甘宁,免疫毒素的诱人武器。
Toxins (Basel). 2018 Aug 8;10(8):323. doi: 10.3390/toxins10080323.
3
The Use of Plant-Derived Ribosome Inactivating Proteins in Immunotoxin Development: Past, Present and Future Generations.植物来源核糖体失活蛋白在免疫毒素研发中的应用:过去、现在和未来。
Toxins (Basel). 2017 Oct 27;9(11):344. doi: 10.3390/toxins9110344.
4
Addressing the Immunogenicity of the Cargo and of the Targeting Antibodies with a Focus on Demmunized Bacterial Toxins and on Antibody-Targeted Human Effector Proteins.关注去免疫细菌毒素和抗体靶向的人类效应蛋白,解决载体及靶向抗体的免疫原性问题。
Biomedicines. 2017 Jun 2;5(2):28. doi: 10.3390/biomedicines5020028.
5
Selecting Targets for Tumor Imaging: An Overview of Cancer-Associated Membrane Proteins.肿瘤成像靶点的选择:癌症相关膜蛋白概述
Biomark Cancer. 2016 Sep 27;8:119-133. doi: 10.4137/BIC.S38542. eCollection 2016.
6
Depletion of T cell epitopes in lysostaphin mitigates anti-drug antibody response and enhances antibacterial efficacy in vivo.溶葡萄球菌酶中T细胞表位的缺失可减轻抗药物抗体反应并增强体内抗菌功效。
Chem Biol. 2015 May 21;22(5):629-39. doi: 10.1016/j.chembiol.2015.04.017.
7
Advances in anticancer immunotoxin therapy.抗癌免疫毒素疗法的进展。
Oncologist. 2015 Feb;20(2):176-85. doi: 10.1634/theoncologist.2014-0358. Epub 2015 Jan 5.
8
Immunotoxins constructed with ribosome-inactivating proteins and their enhancers: a lethal cocktail with tumor specific efficacy.免疫毒素由核糖体失活蛋白及其增强子构建:具有肿瘤特异性疗效的致命鸡尾酒。
Curr Pharm Des. 2014;20(42):6584-643. doi: 10.2174/1381612820666140826153913.
9
PSMA, EpCAM, VEGF and GRPR as imaging targets in locally recurrent prostate cancer after radiotherapy.PSMA、EpCAM、VEGF和GRPR作为放疗后局部复发性前列腺癌的成像靶点。
Int J Mol Sci. 2014 Apr 10;15(4):6046-61. doi: 10.3390/ijms15046046.
10
The functionalized human serine protease granzyme B/VEGF₁₂₁ targets tumor vasculature and ablates tumor growth.功能化的人丝氨酸蛋白酶颗粒酶 B/VEGF₁₂₁靶向肿瘤血管,并消融肿瘤生长。
Mol Cancer Ther. 2013 Oct;12(10):2055-66. doi: 10.1158/1535-7163.MCT-13-0165. Epub 2013 Jul 15.