英夫利昔单抗
医学
药代动力学
结肠炎
肿瘤坏死因子α
胃肠病学
溃疡性结肠炎
免疫学
药理学
药效学
内科学
疾病
作者
Loris Riccardo Lopetuso,Valentina Petito,Valerio Cufino,Vincenzo Arena,Egidio Stigliano,Viviana Gerardi,Eleonora Gaetani,Andrea Poscia,Arianna Amato,Giovanni Cammarota,Alfredo Papa,Alessandro Sgambato,Antonio Gasbarrini,Franco Scaldaferri
标识
DOI:10.1016/j.dld.2013.06.007
摘要
Infliximab is effective in human and murine IBD, but its pharmacodynamic is still poorly known. The aim of this study was to assess the affinity of infliximab to murine TNF-α, its role in murine colitis when administered intra-rectally and its levels in the blood, gut mucosa and stool of healthy and sick mice.An ELISA kit was built in order to assess the affinity of infliximab to human or murine-TNF-α. Human IgG were used as controls. DSS model of colitis on C57BL/6 mice was used to assess clinical efficacy of infliximab administered intravenously or by enema. Stool, serum and colon samples were collected to assess infliximab levels and histology for Rachmilewitz score.Infliximab showed a good affinity both for human-TNF-α and murine-TNF-α. In DSS colitic mice infliximab ameliorated the severity of colitis, regardless of the administration route. In comparison with colitic mice, healthy mice displayed higher serum and mucosal infliximab levels, while detectable levels of infliximab were found in faeces, particularly in colitic mice.Our data support murine models to study infliximab pharmacokinetics and dynamics. Measurable levels of infliximab can be found at different concentrations in blood, intestinal mucosa and stool from healthy and sick mice, thus infliximab pharmacokinetics could have a major impact in human IBD.
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