单克隆抗体
淋巴瘤
Jurkat细胞
流式细胞术
CD19
抗体
嵌合抗原受体
造血
分子生物学
癌症研究
遗传增强
单克隆
抗原
医学
细胞疗法
免疫学
免疫疗法
兔子(密码)
细胞培养
化学
受体
生物
抗体疗法
细胞
双特异性抗体
单克隆抗体治疗
细胞表面受体
作者
Huixin Li,Qiqi Lu,Xin Huang,Mengyan Li,Yiting Zhou,Mengjuan Chen,Mengke Qin,Jingjing Kang,Shanshan Xie,Qingda Meng
摘要
Lymphoma constitutes 24% of canine neoplastic diseases and 85% of haematopoietic tumours, with B-cell subtypes accounting for 60%-80% of cases. As the most prevalent spontaneous tumour in canines, this disease model holds significant translational value for human non-Hodgkin lymphoma research. To address diagnostic limitations in canine B-cell lymphoma, we developed a canine-specific CD19 monoclonal antibody (HAC19.1) with high affinity and established a dual-platform detection system compatible with flow cytometry and immunohistochemistry. Additionally, a novel CD19-targeting chimeric antigen receptor (CAR) gene sequence (HUA-1) was engineered and successfully transduced into Jurkat cells via lentiviral vectors, confirming stable CAR membrane expression. This breakthrough provides critical technical groundwork for advancing autologous CAR-T cell therapy in canines.
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