Suppr超能文献

有效的肿瘤靶向:武装抗体递送策略

Effective tumor targeting: strategies for the delivery of Armed Antibodies.

作者信息

MacDonald Glen C, Glover Nick

机构信息

Viventia Biotech Inc, 147 Hamelin Street, Winnipeg, Manitoba R3T 3Z1, Canada.

出版信息

Curr Opin Drug Discov Devel. 2005 Mar;8(2):177-83.

Abstract

It has long been realized that the presence of tumor-associated antigens offers an excellent opportunity for targeted cancer therapy and hence an improved clinical benefit for cancer patients. Advances in the field of antibody engineering as well as the characterization of toxins, such as diphtheria toxin and Pseudomonas exotoxin A, have enabled the routine construction of recombinant immunotoxins, which we have termed Armed Antibodies. The selective toxicity and mechanism of action of these molecules could potentially provide an excellent clinical alternative to conventional anticancer agents which have many unacceptable side effects. Although considerable clinical success has been achieved using immunotoxin therapy, particularly for B-cell malignancies, the treatment of solid tumors remains highly challenging. To successfully treat solid tumors that are not amenable to local therapy, immunotoxins must be designed to permit repeat systemic administration. This review outlines some of the strategies currently being employed in the design of the Viventia Biotech Inc Armed Antibodies to minimize the development of immunogenicity and to remove the potential for toxicity in non-target tissues.

摘要

长期以来,人们已经认识到肿瘤相关抗原的存在为靶向癌症治疗提供了绝佳机会,从而为癌症患者带来更好的临床益处。抗体工程领域的进展以及毒素(如白喉毒素和铜绿假单胞菌外毒素A)的特性研究,使得重组免疫毒素的常规构建成为可能,我们将其称为武装抗体。这些分子的选择性毒性和作用机制有可能为具有许多不可接受副作用的传统抗癌药物提供绝佳的临床替代方案。尽管使用免疫毒素疗法已经取得了相当大的临床成功,尤其是在治疗B细胞恶性肿瘤方面,但实体瘤的治疗仍然极具挑战性。为了成功治疗无法进行局部治疗的实体瘤,免疫毒素必须设计成允许重复全身给药。本综述概述了目前在Viventia Biotech Inc武装抗体设计中采用的一些策略,以尽量减少免疫原性的产生,并消除非靶组织中毒性的可能性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验