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Tumor-Antigen-Binding Bispecific Antibodies for Cancer Treatment

机译:肿瘤抗原结合双特异性抗体用于癌症治疗

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Bi- and multispecific antibody derivatives (bsAbs) can be considered as the next generation of targeted biologics for cancer therapy. The general concept of bsAbs is a physical connection of recombinant antibody-derived entities with at least two binding specificities. This generates bsAbs that bind at least two antigens or epitopes, thus altering their binding functionalities and specificities in comparison to "normal" antibodies. Most bsAbs are produced as recombinant proteins, either as large IgG-like proteins that contain Fc regions, or as smaller entities with multiple antigen-binding regions but without Fc. Application of bsAbs in experimental cancer therapy currently includes molecules that bind different cell surface proteins to achieve more complete blockage of proliferative or angiogenesis-associated pathways. This approach of blocking more than one pathway component, or to simultaneously hit complementing pathways, also may limit potential escape mechanisms of cancer cells. BsAbs also are applied in the clinic as vehicles to deliver immune effector cells and/or cytokines to tumors. (C) 2014 The Authors. Published by Elsevier Inc. All rights reserved. This is an open access article under the CC BY-NC-ND license (hap://creativecommons.org/licenses/by-nc-nd/3.0/).
机译:双特异性抗体衍生物和多特异性抗体衍生物(bsAbs)可被视为下一代癌症治疗的靶向生物制剂。 bsAbs的一般概念是具有至少两个结合特异性的重组抗体衍生实体的物理连接。这产生了结合至少两种抗原或表位的bsAb,因此与“正常”抗体相比改变了它们的结合功能和特异性。大多数bsAb均以重组蛋白,包含Fc区的大型IgG类蛋白或具有多个抗原结合区但不含Fc的较小实体的形式产生。目前,bsAb在实验性癌症治疗中的应用包括结合不同细胞表面蛋白的分子,以实现对增殖或血管生成相关途径的更完全阻断。这种阻断一种以上途径成分或同时命中补体途径的方法也可能限制癌细胞的潜在逃逸机制。 BsAb在临床上也用作将免疫效应细胞和/或细胞因子递送至肿瘤的载体。 (C)2014作者。由Elsevier Inc.出版。保留所有权利。这是CC BY-NC-ND许可(hap://creativecommons.org/licenses/by-nc-nd/3.0/)下的开放获取文章。

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