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Production of Human Monoclonal Antibodies Against FC Epsilon Receptor I Alpha by Combining In Vitro Immunization with Phage Display

机译:通过将体外免疫与噬菌体展示组合来生产对Fcε受体Iα的人单克隆抗体的生产

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Monoclonal antibodies (mAbs) have a great potential and hope for the treatment of various human diseases. The advent of mAbs was done using hybridoma technology, which was introduced by Kohler and Milstein. However, owing to their murine origins, thefirst generation of mAbs evaluated in the clinic was limited by their immunogenicity. Thus, increasing effort has been applied to engineer antibodies without a non-human structure to minimize such responses. To overcome this problem, we developed an in vitro immunization (IVI) protocol, which elicits antigen-specific immune responses in peripheral blood mononuclear cells (PBMC). In antibody engineering, cell surface antigens are often targeted as they play an increasingly important role. However the generation of antibodies against cell surface antigens is hard owing to the difficulty in obtaining sufficient amounts of antigen with high purity and in the native conformation for immunization.
机译:单克隆抗体(MAB)具有巨大的潜力和希望治疗各种人类疾病。 MAB的出现是使用杂交瘤技术完成的,该技术由科勒和米尔斯坦引入。然而,由于它们的鼠起源,在临床中评价的缺乏的MAbs受其免疫原性的限制。因此,越来越多的努力已经应用于没有非人结构的工程抗体,以最小化这些反应。为了克服这个问题,我们开发了一种体外免疫(IVI)方案,其引发了外周血单核细胞(PBMC)中的抗原特异性免疫应答。在抗体工程中,细胞表面抗原通常靶向,因为它们起着越来越重要的作用。然而,由于难以获得具有高纯度的足够量的抗原和用于免疫的天然构象的难以获得足够的抗原,因此抗细胞表面抗原的抗体的产生难以努力。

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