Ye Xueshi, Li Wanli, Huang Jinwen, Zhang Lifei, Zhang Ye
Department of Hematology, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Department of Orthopedics, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Front Oncol. 2020 Nov 20;10:587237. doi: 10.3389/fonc.2020.587237. eCollection 2020.
To date, multiple myeloma remains an incurable disease. Immunotherapy is an encouraging option in the development of multiple myeloma (MM) therapy. CS1 is a specific myeloma antigen, which is highly expressed in myeloma cells. Calreticulin (CRT) is a key determinant of cell death, which can influence antigen presentation and promote cellular phagocytic uptake. In the current study, we constructed a DNA vaccine encoding both CS1 and CRT. Our results show that the PcDNA3.1-CS1/CRT vaccine was able to induce cytotoxic T cell responses against myeloma cells , and the tumor growth was significantly suppressed in mice immunized with this vaccine. Therefore, our findings indicate that the CS1/CRT fusion DNA vaccine may represent a promising novel myeloma therapy, and the potential for combining the CS1/CRT vaccine with other myeloma treatments.
迄今为止,多发性骨髓瘤仍然是一种无法治愈的疾病。免疫疗法是多发性骨髓瘤(MM)治疗发展中一个令人鼓舞的选择。CS1是一种特异性骨髓瘤抗原,在骨髓瘤细胞中高度表达。钙网蛋白(CRT)是细胞死亡的关键决定因素,它可影响抗原呈递并促进细胞吞噬摄取。在本研究中,我们构建了一种编码CS1和CRT的DNA疫苗。我们的结果表明,PcDNA3.1-CS1/CRT疫苗能够诱导针对骨髓瘤细胞的细胞毒性T细胞反应,并且在用该疫苗免疫的小鼠中肿瘤生长受到显著抑制。因此,我们的研究结果表明,CS1/CRT融合DNA疫苗可能是一种有前景的新型骨髓瘤治疗方法,以及将CS1/CRT疫苗与其他骨髓瘤治疗方法联合使用的潜力。