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

被引:24
|
作者
Iberg, Courtney A. [1 ]
Hawiger, Daniel [1 ]
机构
[1] St Louis Univ, Sch Med, Doisy Res Ctr, Dept Mol Microbiol & Immunol, 1205 Carr Lane, St Louis, MO 63104 USA
基金
美国国家卫生研究院;
关键词
Recombinant chimeric antibody; Immunotherapy; Immunomodulation; Autoimmunity; Cancer; DEC-205; C-TYPE LECTIN; PLASMACYTOID DENDRITIC CELLS; REGULATORY T-CELLS; STEADY-STATE; IMMUNE-RESPONSES; ENDOCYTIC RECEPTOR; LANGERHANS CELLS; TARGETING ANTIGENS; DISTINCT SUBSETS; HUMAN TISSUES;
D O I
10.1016/j.intimp.2019.05.037
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:575 / 580
页数:6
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