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ELPylated anti‐human TNF therapeutic single‐domain antibodies for prevention of lethal septic shock

机译:烯醇化的抗人TNF治疗单结构域抗体,用于预防致命化脓性休克

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Summary Tumour necrosis factor (TNF) is a major pro-inflammatory cytokine involved in multiple inflammatory diseases. The detrimental activity of TNF can be blocked by various antagonists, and commercial therapeutics based upon this principle have been approved for treatment of diseases including rheumatoid arthritis, Crohn’s disease and psoriasis. In a search for new, improved anti-inflammatory therapeutics we have designed a single-domain monoclonal antibody (VsubH/subH), which recognizes TNF. The antibody component (TNF-VsubH/subH) is based upon an anti-human TNF Camelidae heavy-chain monoclonal antibody, which was linked to an elastin-like polypeptide (ELP). We demonstrate that ELP fusion to the TNF-VsubH/subH enhances accumulation of the fusion protein during biomanufacturing in transgenic tobacco plants. With this study, we show for the first time that this plant-derived anti-human TNF-VsubH/subH antibody was biologically active in vivo . Therefore, therapeutic application of TNF-VsubH/subH-ELP fusion protein was tested in humanized TNF mice and was shown to be effective in preventing death caused by septic shock. The in vivo persistence of the ELPylated antibody was ∼24 fold longer than that of non-ELPylated TNF-VsubH/subH.
机译:发明内容肿瘤坏死因子(TNF)是涉及多种炎症性疾病的主要炎症细胞因子。 TNF的有害活性可以被各种拮抗剂阻断,并且基于该原则的商业治疗方法已被批准用于治疗包括类风湿性关节炎,克罗恩病和牛皮癣等疾病。在寻找新的,改进的抗炎治疗剂中,我们设计了一种识别TNF的单域单克隆抗体(V H H)。抗体组分(TNF-V <亚> H)基于抗人TNF Camelidae重链单克隆抗体,其与弹性蛋白的多肽(ELP)连接。我们证明ELP融合到TNF-V <亚> H H增强了转基因烟草植物生物制造过程中融合蛋白的积累。通过这项研究,我们首次显示这种植物衍生的抗人类TNF-V <亚> H H抗体在体内生物活性活性。因此,在人源化TNF小鼠中测试了TNF-V H H-ELP融合蛋白的治疗施加,并且显示有效地预防由脓肠梗休克引起的死亡。烯烯化抗体的体内持续性比非elpylated TNF-V H H的倍数〜24倍。

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