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新型口服抗肿瘤坏死因子结构域抗体的临床前开发用于治疗炎症性肠病。

Preclinical Development of a Novel, Orally-Administered Anti-Tumour Necrosis Factor Domain Antibody for the Treatment of Inflammatory Bowel Disease.

机构信息

VHsquared Ltd., 1 Lower Court, Copley Hill, Cambridge Road, Babraham, Cambridge, CB22 3GN, UK.

Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK.

出版信息

Sci Rep. 2018 Mar 21;8(1):4941. doi: 10.1038/s41598-018-23277-7.

Abstract

TNFα is an important cytokine in inflammatory bowel disease. V565 is a novel anti-TNFα domain antibody developed for oral administration in IBD patients, derived from a llama domain antibody and engineered to enhance intestinal protease resistance. V565 activity was evaluated in TNFα-TNFα receptor-binding ELISAs as well as TNFα responsive cellular assays and demonstrated neutralisation of both soluble and membrane TNFα with potencies similar to those of adalimumab. Although sensitive to pepsin, V565 retained activity after lengthy incubations with trypsin, chymotrypsin, and pancreatin, as well as mouse small intestinal and human ileal and faecal supernatants. In orally dosed naïve and DSS colitis mice, high V565 concentrations were observed in intestinal contents and faeces and immunostaining revealed V565 localisation in mouse colon tissue. V565 was detected by ELISA in post-dose serum of colitis mice, but not naïve mice, demonstrating penetration of disrupted epithelium. In an ex vivo human IBD tissue culture model, V565 inhibition of tissue phosphoprotein levels and production of inflammatory cytokine biomarkers was similar to infliximab, demonstrating efficacy when present at the disease site. Taken together, results of these studies provide confidence that oral V565 dosing will be therapeutic in IBD patients where the mucosal epithelial barrier is compromised.

摘要

TNFα 是炎症性肠病中的一种重要细胞因子。V565 是一种新型的抗 TNFα 结构域抗体,旨在为 IBD 患者开发口服制剂,源自骆驼科动物的抗体,经过工程改造以增强对肠道蛋白酶的抗性。V565 的活性在 TNFα-TNFα 受体结合 ELISA 以及 TNFα 反应性细胞测定中进行了评估,并证明其能够中和可溶性和膜结合 TNFα,其效价与阿达木单抗相当。尽管对胃蛋白酶敏感,但 V565 在与胃蛋白酶、胰凝乳蛋白酶和胰酶以及小鼠小肠和人回肠和粪便上清液长时间孵育后仍保持活性。在口服给予的 naive 和 DSS 结肠炎小鼠中,在肠内容物和粪便中观察到高浓度的 V565,免疫染色显示 V565 在小鼠结肠组织中的定位。在结肠炎小鼠的给药后血清中通过 ELISA 检测到 V565,但在 naive 小鼠中未检测到,表明上皮细胞被破坏后 V565 能够穿透。在体外人类 IBD 组织培养模型中,V565 抑制组织磷酸蛋白水平和炎症细胞因子生物标志物的产生与英夫利昔单抗相似,表明在疾病部位存在时具有疗效。综上所述,这些研究的结果表明,口服 V565 给药将在肠黏膜上皮屏障受损的 IBD 患者中具有治疗作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75c7/5862986/6492ce25d844/41598_2018_23277_Fig1_HTML.jpg

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