Antibody Isotypes for Tumor Immunotherapy

被引:46
作者
Kretschmer, Anna
Schwanbeck, Ralf
Valerius, Thomas
Roesner, Thies [1 ,2 ]
机构
[1] Univ Hosp Schleswig Holstein, Div Stem Cell Transplantat & Immunotherapy, Dept Med 2, Arnold Heller Str 3, D-24105 Kiel, Germany
[2] Univ Kiel, Arnold Heller Str 3, D-24105 Kiel, Germany
关键词
Cancer; Immune response; Immunoglobulin isotypes; Immunotherapy; FAB-ARM EXCHANGE; GROWTH-FACTOR RECEPTOR; IN-VIVO; FC-RECEPTOR; MONOCLONAL-ANTIBODIES; EFFECTOR MECHANISMS; IGE IMMUNOTHERAPY; IGG4; ANTIBODIES; CANCER CELLS; COMPLEMENT;
D O I
10.1159/000479240
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Compared to the evolutionary diversity of antibody iso-types, the spectrum of currently approved therapeutic antibodies is biased to the human IgG1 isotype. Detailed studies into the different structures and functions of human isotypes have suggested that other isotypes than IgG1 may be advantageous for specific indications - depending on the complex interplay between the targeted antigen or epitope, the desired mode of action, the pharmacokinetic properties, and the biopharmaceutical considerations. Thus, it may be speculated that with the increasing number of antibodies becoming available against a broadening spectrum of target antigens, identification of the optimal antibody isotype for particular therapeutic applications may become critical for the therapeutic success of individual antibodies. Thus, investments into this rather unexplored area of antibody immunotherapy may provide opportunities for distinction in the increasingly busy 'antibody space'. Therefore, IgG, IgA, IgE as well as IgM isotypes will be discussed in this review. (C) 2017 S. Karger GmbH, Freiburg
引用
收藏
页码:320 / 326
页数:7
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