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利用重组嵌合抗体通过体内抗原递送至 DEC-205 和其他细胞表面分子来推进免疫调节。

Advancing immunomodulation by in vivo antigen delivery to DEC-205 and other cell surface molecules using recombinant chimeric antibodies.

机构信息

Department of Molecular Microbiology and Immunology, Saint Louis University School of Medicine, Doisy Research Center, 1205 Carr Lane, St. Louis, MO 63104, USA.

Department of Molecular Microbiology and Immunology, Saint Louis University School of Medicine, Doisy Research Center, 1205 Carr Lane, St. Louis, MO 63104, USA.

出版信息

Int Immunopharmacol. 2019 Aug;73:575-580. doi: 10.1016/j.intimp.2019.05.037. Epub 2019 Jun 19.

Abstract

A targeted delivery of defined antigens in vivo allows for the probing of relevant functions of the immune system. Recombinant chimeric antibodies, produced by genetically modifying original monoclonal antibodies specific for molecules expressed on dendritic cells and other immune cells, have paved the way for the development of such strategies and have become reliable tools for achieving a specific immunomodulation. These antibodies have proven important in both basic research and clinical applications, extending data obtained in disease models of autoimmunity and cancer. Here we will describe the advances gained from the experimental and therapeutic strategies based on the targeting of the specific antigens by recombinant chimeric antibodies to the multilectin receptor DEC-205 and other cell surface molecules.

摘要

在体内靶向递送达特定抗原可用于探测免疫系统的相关功能。通过基因修饰针对树突状细胞和其他免疫细胞表达的分子的原始单克隆抗体而产生的重组嵌合抗体为这些策略的发展铺平了道路,并成为实现特定免疫调节的可靠工具。这些抗体在基础研究和临床应用中都非常重要,它们扩展了在自身免疫和癌症疾病模型中获得的数据。在这里,我们将描述基于通过重组嵌合抗体针对 DEC-205 等多凝集素受体和其他细胞表面分子的特定抗原的靶向作用的实验和治疗策略所取得的进展。

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