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口服抗肿瘤坏死因子域抗体 V565 可提供高肠道浓度,并降低溃疡性结肠炎患者的炎症标志物。

Oral Anti-Tumour Necrosis Factor Domain Antibody V565 Provides High Intestinal Concentrations, and Reduces Markers of Inflammation in Ulcerative Colitis Patients.

机构信息

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

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

出版信息

Sci Rep. 2019 Oct 1;9(1):14042. doi: 10.1038/s41598-019-50545-x.

Abstract

V565 is an engineered TNFα-neutralising single domain antibody formulated into enteric coated mini-tablets to enable release in the intestine after oral administration as a possible oral treatment for inflammatory bowel disease (IBD). Following oral administration, ileal recovery of V565 was investigated in four patients with terminal ileostomy. Intestinal and systemic pharmacokinetics were measured in six patients with Crohn's disease and evidence of target engagement assessed in five patients with ulcerative colitis. Following oral administration, V565 was detected at micromolar concentrations in ileal fluid from the ileostomy patients and in stools of the Crohn's patients. In four of the five ulcerative colitis patients, biopsies taken after 7d dosing demonstrated V565 in the lamina propria with co-immunostaining on CD3 T-lymphocytes and CD14 macrophages. Phosphorylation of signalling proteins in biopsies taken after 7d oral dosing was decreased by approximately 50%. In conclusion, enteric coating of V565 mini-tablets provided protection in the stomach with gradual release in intestinal regions affected by IBD. Immunostaining revealed V565 tissue penetration and association with inflammatory cells, while decreased phosphoproteins after 7d oral dosing was consistent with V565-TNFα engagement and neutralising activity. Overall these results are encouraging for the clinical utility of V565 in the treatment of IBD.

摘要

V565 是一种经过工程改造的 TNFα 中和单域抗体,制成肠溶包衣迷你片剂,以便在口服后能在肠道中释放,作为治疗炎症性肠病(IBD)的潜在口服疗法。在口服给药后,在 4 名回肠造口术患者中研究了 V565 在回肠的恢复情况。在 6 名克罗恩病患者中测量了肠道和全身药代动力学,并在 5 名溃疡性结肠炎患者中评估了靶标结合的证据。口服给药后,在回肠造口术患者的回肠液和克罗恩病患者的粪便中均以微摩尔浓度检测到 V565。在 5 名溃疡性结肠炎患者中的 4 名患者中,在 7d 给药后进行的活检显示 V565 存在于固有层中,并与 CD3 T 淋巴细胞和 CD14 巨噬细胞共免疫染色。在 7d 口服给药后进行的活检中,信号蛋白的磷酸化减少了约 50%。总之,V565 迷你片剂的肠溶包衣在胃中提供了保护,同时在受 IBD 影响的肠道区域逐渐释放。免疫染色显示 V565 组织穿透和与炎症细胞的关联,而在 7d 口服给药后磷酸化蛋白减少与 V565-TNFα 结合和中和活性一致。总的来说,这些结果令人鼓舞,表明 V565 在治疗 IBD 方面具有临床应用潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f922/6773840/1a79a3097609/41598_2019_50545_Fig1_HTML.jpg

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