VEGFR2-targeted fusion antibody improved NK cell-mediated immunosurveillance against K562 cells

被引:4
|
作者
Ren, Xueyan [1 ]
Xie, Wei [1 ]
Wang, Youfu [1 ]
Xu, Menghuai [1 ]
Liu, Fang [1 ]
Tang, Mingying [1 ]
Li, Chenchen [1 ]
Wang, Min [1 ]
Zhang, Juan [1 ]
机构
[1] China Pharmaceut Univ, State Key Lab Nat Med, Sch Life Sci & Technol, 154,Tong Jia Xiang 24, Nanjing 210009, Peoples R China
基金
中国国家自然科学基金;
关键词
Antibody fusion protein; Vascular endothelial growth factor receptor 2 (VEGFR2); MHC class I polypeptide-related sequence A (MICA); Immunosurveillance; ENDOTHELIAL GROWTH-FACTOR; CHRONIC MYELOID-LEUKEMIA; CHRONIC MYELOGENOUS LEUKEMIA; TYROSINE KINASE INHIBITORS; PHASE-2; TRIAL; VEGF; ANGIOGENESIS; EXPRESSION; BEVACIZUMAB; GENERATION;
D O I
10.1007/s12026-016-8800-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
MHC class I polypeptide-related sequence A (MICA), which is normally expressed on cancer cells, activates NK cells via NK group 2-member D pathway. However, some cancer cells escape NK-mediated immune surveillance by shedding membrane MICA causing immune suppression. To address this issue, we designed an antibody-MICA fusion targeting tumor-specific antigen (vascular endothelial growth factor receptor 2, VEGFR2) based on our patented antibody (mAb04) against VEGFR2. In vitro results demonstrate that the fusion antibody retains both the antineoplastic and the immunomodulatory activity of mAb04. Further, we revealed that it enhanced NK-mediated immunosurveillance against K562 cells through increasing degranulation and cytokine production of NK cells. The overall data suggest our new fusion protein provides a promising approach for cancer-targeted immunotherapy and has prospects for potential application of chronic myeloid leukemia.
引用
收藏
页码:1060 / 1070
页数:11
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