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一种新型双特异性抗体的特性研究:该抗体通过T细胞结合靶向组织因子阳性肿瘤

Characterization of a novel bispecific antibody targeting tissue factor-positive tumors with T cell engagement.

作者信息

Pan Zhidi, Chen Jie, Xiao Xiaodong, Xie Yueqing, Jiang Hua, Zhang Baohong, Lu Huili, Yuan Yunsheng, Han Lei, Zhou Yuexian, Zong Huifang, Wang Lei, Sun Rui, Zhu Jianwei

机构信息

Engineering Research Center of Cell & Therapeutic Antibody, MOE, School of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, China.

Jecho Laboratories, Inc., Frederick, MD 21704, USA.

出版信息

Acta Pharm Sin B. 2022 Apr;12(4):1928-1942. doi: 10.1016/j.apsb.2021.10.028. Epub 2021 Nov 3.

Abstract

T cell engaging bispecific antibody (TCB) is an effective immunotherapy for cancer treatment. Through co-targeting CD3 and tumor-associated antigen (TAA), TCB can redirect CD3 T cells to eliminate tumor cells regardless of the specificity of T cell receptor. Tissue factor (TF) is a TAA that involved in tumor progression. Here, we designed and characterized a novel TCB targeting TF (TF-TCB) for the treatment of TF-positive tumors. , robust T cell activation, tumor cell lysis and T cell proliferation were induced by TF-TCB. The tumor cell lysis activity was dependent upon both CD3 and TF binding moieties of the TF-TCB, and was related to TF expression level of tumor cells. , in both tumor cell/human peripheral blood mononuclear cells (PBMC) co-grafting model and established tumor models with poor T cell infiltration, tumor growth was strongly inhibited by TF-TCB. T cell infiltration into tumors was induced during the treatment. Furthermore, efficacy of TF-TCB was further improved by combination with immune checkpoint inhibitors. For the first time, our results validated the feasibility of using TF as a target for TCB and highlighted the potential for TF-TCB to demonstrate efficacy in solid tumor treatment.

摘要

T细胞接合双特异性抗体(TCB)是一种用于癌症治疗的有效免疫疗法。通过共同靶向CD3和肿瘤相关抗原(TAA),TCB可以重定向CD3 T细胞以消除肿瘤细胞,而不考虑T细胞受体的特异性。组织因子(TF)是一种参与肿瘤进展的TAA。在此,我们设计并表征了一种靶向TF的新型TCB(TF-TCB)用于治疗TF阳性肿瘤。TF-TCB可诱导强烈的T细胞活化、肿瘤细胞裂解和T细胞增殖。肿瘤细胞裂解活性依赖于TF-TCB的CD3和TF结合部分,并且与肿瘤细胞的TF表达水平相关。在肿瘤细胞/人外周血单核细胞(PBMC)共移植模型和T细胞浸润较差的既定肿瘤模型中,TF-TCB均强烈抑制肿瘤生长。治疗期间可诱导T细胞浸润到肿瘤中。此外,TF-TCB与免疫检查点抑制剂联合使用可进一步提高疗效。我们的结果首次验证了将TF用作TCB靶点的可行性,并突出了TF-TCB在实体瘤治疗中显示疗效的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c9a/9279644/bc141931e4aa/ga1.jpg

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