Considerations for Combined Immune Checkpoint Modulation and Radiation Treatment

被引:5
作者
Almoa, Steven C. [1 ,2 ]
Guha, Chandan [3 ,4 ]
机构
[1] Albert Einstein Coll Med, Dept Biochem, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Dept Physiol & Biophys, Bronx, NY 10461 USA
[3] Albert Einstein Coll Med, Dept Pathol, Bronx, NY 10461 USA
[4] Albert Einstein Coll Med, Montefiore Med Ctr, Dept Radiat Oncol, Bronx, NY 10461 USA
关键词
LONG-TERM SURVIVAL; T-CELL-ACTIVATION; COSTIMULATION BLOCKADE; RHEUMATOID-ARTHRITIS; STRUCTURAL GENOMICS; IONIZING-RADIATION; CRYSTAL-STRUCTURE; DWELL-TIME; CANCER; LIGAND;
D O I
10.1667/RR13667.1
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Recent advances indicate that new therapeutic strategies for the treatment of malignancies will be realized from combined radiation treatment and immune checkpoint modulation. Numerous biophysical properties must be considered for effective biologic development, including affinity, selectivity, oligomeric state and valency. High-resolution structural characterization contributes to our understanding of these properties and can lead to the realization of proteins with unique in vitro activities and novel in vivo therapeutic functions. In this article we focus on the importance of these factors for new potential biologics and consider these in the context of combination therapies with physical modalities, including radiation therapy. In particular, we examine the consequences of altered avidities and subset-specific ligand density on the rational modification of biological function in the immunoglobulin and tumor necrosis factor superfamilies and for new optimized combination therapies. (C) 2014 by Radiation Research Society
引用
收藏
页码:230 / 238
页数:9
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