Preclinical characterization of Pan-NKG2D ligand-binding NKG2D receptor decoys

被引:0
作者
Rupert, Peter B. [1 ]
Buerger, Matthew [1 ]
Girard, Emily J. [2 ,3 ]
Frutoso, Marie [1 ,4 ]
Parrilla, Don [1 ,5 ]
Ng, Kevin [1 ]
Gooley, Theodore [1 ]
Groh, Veronika [1 ]
Strong, Roland K. [1 ]
机构
[1] Fred Hutchinson Canc Ctr, Div Basic Sci, Seattle, WA 98109 USA
[2] Fred Hutchinson Canc Ctr, Clin Res Div, Seattle, WA USA
[3] Seattle Childrens Res Inst, Ben Towne Ctr Childhood Canc Res, Renton, WA USA
[4] Univ Brest, LBAI, UMRI 1227, Inserm, Brest, France
[5] Umoja Biopharm, Seattle, WA USA
基金
美国国家卫生研究院;
关键词
Natural killer cell receptors; NKG2D; Engineered biologic immunotherapeutics; X-ray crystallography; IMMUNORECEPTOR NKG2D; LYMPHOCYTE RECEPTOR; CCP4; SUITE; T-CELLS; PROTEIN; EXPRESSION; ASSOCIATION; ACTIVATION; INDUCTION;
D O I
10.1016/j.heliyon.2024.e28583
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
NKG2D and its ligands are critical regulators of protective immune responses controlling infections and cancer, defining a crucial immune signaling axis. Current therapeutic efforts targeting this axis almost exclusively aim at enhancing NKG2D-mediated effector functions. However, this axis can drive disease processes when dysregulated, in particular, driving stem -like cancer cell reprogramming and tumorigenesis through receptor/ligand self -stimulation on tumor cells. Despite complexities with its structure and biology, we developed multiple novel engineered proteins that functionally serve as axis -blocking NKG2D "decoys " and report biochemical, structural, in vitro , and in vivo evaluation of their functionality.
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页数:13
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