首页> 美国卫生研究院文献>Scientific Reports >Oral Anti-Tumour Necrosis Factor Domain Antibody V565 Provides High Intestinal Concentrations and Reduces Markers of Inflammation in Ulcerative Colitis Patients
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Oral Anti-Tumour Necrosis Factor Domain Antibody V565 Provides High Intestinal Concentrations and Reduces Markers of Inflammation in Ulcerative Colitis Patients

机译:口腔抗肿瘤坏死因子域抗体V565可提供高肠道浓度并减少溃疡性结肠炎患者的炎症标记

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摘要

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.
机译:V565是一种经过工程改造的TNFα中和性单结构域抗体,配制成肠溶包衣的小片剂,可以口服给药后在肠道内释放,作为炎症性肠病(IBD)的可能口服治疗方法。口服后,对四名终末回肠造口术患者进行了V565的回肠恢复研究。对六名克罗恩病患者的肠道和全身药代动力学进行了测量,并对五名溃疡性结肠炎患者进行了靶标参与的评估。口服后,从回肠造口术患者和克罗恩病患者粪便中回肠液中以微摩尔浓度检测到V565。在五名溃疡性结肠炎患者中,有四名在7d给药后进行活检,发现固有层中存在V565,并在CD3 + T淋巴细胞和CD14 + 巨噬细胞上进行了免疫共染色。口服7d后进行的活检中信号蛋白的磷酸化降低了约50%。总之,V565迷你片剂的肠溶衣可在受IBD影响的肠道区域逐渐释放的情况下提供对胃的保护。免疫染色显示V565组织渗透并与炎性细胞缔合,而口服7d后磷蛋白减少与V565-TNFα参与和中和活性一致。总体而言,这些结果对于V565在IBD治疗中的临床应用令人鼓舞。

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