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Properties of Fluorescent Far-Red Anti-TNF Nanobodies

机译:荧光远红抗TNF纳米抗体的性质

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摘要

Upregulation of the expression of tumor necrosis factor (TNF-α, TNF) has a significant role in the development of autoimmune diseases. The fluorescent antibodies binding TNF may be used for personalized therapy of TNF-dependent diseases as a tool to predict the response to anti-TNF treatment. We generated recombinant fluorescent proteins consisting of the anti-TNF module based on the variable heavy chain (VHH) of camelid antibodies fused with the far-red fluorescent protein Katushka (Kat). Two types of anti-TNF VHH were developed: one (BTN-Kat) that was bound both human or mouse TNF, but did not neutralize their activity, and a second (ITN-Kat) that was binding and neutralizing human TNF. BTN-Kat does not interfere with TNF biological functions and can be used for whole-body imaging. ITN-Kat can be evaluated in humanized mice or in cells isolated from humanized mice. It is able to block human TNF (hTNF) activities both in vitro and in vivo and may be considered as a prototype of a theranostic agent for autoimmune diseases.
机译:肿瘤坏死因子(TNF-α,TNF)表达的上调在自身免疫疾病的发展中具有重要作用。结合TNF的荧光抗体可以用于TNF依赖性疾病的个性化治疗,作为预测对抗TNF治疗的反应的工具。我们产生了重组荧光蛋白,该蛋白由基于与远红色荧光蛋白Katushka(Kat)融合的骆驼科动物抗体的可变重链(VHH)的抗TNF模块组成。已开发出两种类型的抗TNF VHH:一种(BTN-Kat)与人或小鼠TNF结合,但不中和其活性,另一种(ITN-Kat)与人TNF结合并中和。 BTN-Kat不干扰TNF的生物学功能,可用于全身成像。可以在人源化小鼠或从人源化小鼠分离的细胞中评估ITN-Kat。它能够在体外和体内阻断人TNF(hTNF)的活性,并且可以被认为是自身免疫性疾病治疗试剂的原型。

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