TIM-3 blockade combined with bispecific antibody MT110 enhances the anti-tumor effect of γδ T cells

Springer Science and Business Media LLC - Tập 69 - Trang 2571-2587 - 2020
Qingming Guo1,2, Peng Zhao2, Zhen Zhang3, Jinyu Zhang1, Zheng Zhang1, Yanan Hua1, Bin Han4, Ning Li1, Xiaowen Zhao2, Lin Hou1
1Department of Biochemistry and Molecular Biology, School of Basic Medicine, Qingdao University, Qingdao, China
2Clinical Laboratory, Qingdao Central Hospital, The Second Affiliated Hospital of Qingdao University, Qingdao, China
3Radiotherapy Department, Qingdao Central Hospital, The Second Affiliated Hospital of Qingdao University, Qingdao, China
4Institute of Transfusion Medicine, Qingdao Blood Center, Qingdao, People’s Republic of China

Tóm tắt

As ideal cells that can be used for adoptive cell therapy, γδ T cells are a group of homogeneous cells with high proliferative and tumor killing ability. However, γδ T cells are apt to apoptosis and show decreased cytotoxicity under persistent stimulation in vitro and cannot aggregate at tumor sites efficiently in vivo, both of which are two main obstacles to tumor adoptive immunotherapy. In this study, we found that the immune checkpoint T-cell immunoglobulin domain and mucin domain 3 (TIM-3) were up-regulated significantly on γδ T cells during their ex vivo expansion and this up-regulation contributed to the dysfunction of γδ T cells. Although the killing ability of γδ T cells against breast cancer cells which exhibited a high level of epithelial cell adhesion molecule (EpCAM) was enhanced, the level of TIM-3 on γδ T cells was also further up-regulated under the application of the bispecific antibody MT110 (anti-CD3 × anti-EpCAM) which can redirect T cells to target cells. Besides, these γδ T cells with up-regulated TIM-3 exhibited an increased susceptibility to apoptosis. By reinvigorating dysfunctional γδ T cells and promoting them to accumulate at tumor sites, the combined use of TIM-3 inhibitor and MT110 could further enhance the anti-tumor effect of the adoptively transfused γδ T cells. These results may have clinical implications for the design of new translational anti-tumor regimens aimed at combining checkpoint blockade and immune cell redirection.

Tài liệu tham khảo

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