Jones Tim D, Crompton Laura J, Carr Frank J, Baker Matthew P
Antitope Ltd., Babraham, Cambridge, UK.
Methods Mol Biol. 2009;525:405-23, xiv. doi: 10.1007/978-1-59745-554-1_21.
Immunogenicity is a major limitation to therapy with certain monoclonal antibodies and proteins. A major driver for immunogenicity is the presence of human T-cell epitopes within the protein sequence which can activate helper T-cells resulting in the sustained production of antibodies and neutralization of the therapeutic effect. Deimmunization is a new technology for location and removal of T-cell epitopes through the combined use of immunological and molecular biology techniques. In the case of deimmunization of antibodies, mutations to remove T-cell epitopes can generally be introduced without significantly reducing the binding affinity of the antibody. Typically, "deimmunized" antibodies are created with human constant regions and by expression of genes encoding these antibodies in mammalian cells. This chapter details a method for creation of a deimmunized antibody for production in mammalian cells.
免疫原性是某些单克隆抗体和蛋白质治疗的主要限制因素。免疫原性的一个主要驱动因素是蛋白质序列中存在人类T细胞表位,其可激活辅助性T细胞,导致抗体持续产生并中和治疗效果。去免疫是一种通过联合使用免疫学和分子生物学技术来定位和去除T细胞表位的新技术。就抗体去免疫而言,通常可以引入去除T细胞表位的突变,而不会显著降低抗体的结合亲和力。典型地,“去免疫”抗体是用人恒定区并通过在哺乳动物细胞中表达编码这些抗体的基因产生的。本章详细介绍了一种在哺乳动物细胞中产生去免疫抗体的方法。