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首页> 外文期刊>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结构域抗体V565提供高肠浓度,减少溃疡性结肠炎患者炎症的标志物

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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 CD3sup+/sup T-lymphocytes and CD14sup+/sup 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是一种工程化TNFα-中和单结构域抗体,其配制成肠溶型迷你片剂,以使口服给药后肠道释放,作为炎症性肠病的可能口服治疗?(IBD)。口服施用后,在四个末端ortoferomy患者中研究了V565的eLEAL回收率。肠道和全身药代动力学在六位患有克罗恩病的患者中测量,并在五名溃疡性结肠炎患者中评估的目标参与证据。口服给药后,在来自对胃肠杆菌患者的髂骨流体中的微摩尔浓度和克罗恩患者的粪便中检测到V565。在五种五种溃疡性结肠炎患者中,7D给药后进行的活组织检查在薄层丙蛋白中显示V565,在CD3 + T淋巴细胞和CD14 + 巨噬细胞上进行了共免疫染色。 7D口服给药后,在7D口服给药后的信号蛋白的磷酸化降低约50%。总之,V565迷你片剂的肠溶涂层在胃中提供了保护,肠道内逐渐释放,受IBD影响的肠区域。免疫染色揭示了V565组织渗透和与炎性细胞的关系,而7D口服给药后的磷蛋白均与V565-TNFα接合和中和活性一致。总体而言,这些结果是令人鼓舞的v565在治疗IBD的临床用途。

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