姓名:张伟锋
职称/职务:副教授
电话:
传真:
电子信箱:zweifeng@snnu.edu.cn
研究方向:恶性脑胶质瘤的免疫逃逸机制和免疫治疗;神经炎性疾病的发病机制和治疗
办公地点:格物楼3407
一、个人简介
副教授,硕士生导师。2014年获得博士学位,博士期间从事基因治疗相关研究工作;2017-2021年在美国从事3年多的博士后工作,博士后期间针对神经系统自免疫疾病的发病机制和治疗开展研究。在国际顶级期刊Sci Immunol, JCI, Sci Trans Med, PNAS, Cell Mol Immunol, Front Immunol等发表论文20多篇;申报专利8项,已授权7项;主持或参与国家自然科学基金、陕西省自然科学基金、中央高校基金等科研项目14项;担任International Journal of Immunology编委;Molecular Therapy-Nucleic Acids、International Journal of Biological Sciences、Molecular Therapy - Methods & Clinical Development、Molecular Neurobiology等国际知名杂志的审稿人。
二、主要研究领域及兴趣
我国十四五”规划和2035年远景目标刚要中,“脑科学”正式被列为八大战略性基础核心领域之一。本实验室的研究主要聚焦于神经系统炎症相关疾病的发病机制和治疗方法、脑胶质瘤的免疫逃逸机制和免疫治疗。希望通过对影响人类健康的中枢神经系统重大疾病发病机制的探索,发掘新的治疗手段,并实现向临床应用的转化。
三、承担的科研项目
1. 陕西省科技厅重点研发计划项目,2021ZDLSF03-09,基于靶向性外泌体递送芬戈莫德治疗脱髓鞘疾病的应用研究,2021/01/01-2023-12-31,主要参与人;
2. 陕西省科技厅科技新星项目,2019KJXX-022,基于双信号-共培养体系的促髓鞘形成天然药物筛选及其作用机制研究,2019/01/01-2021-12-31,主要参与人;
3. 国家自然科学基金面上项目,81771345,黄芩苷促进少突胶质前体细胞分化及髓鞘再生 的PPARγ/NFIL3信号转导机制,2018/01/01-2021/12/31,主要参与人;
4. 国家自然科学基金面上项目,81773265,基于双靶分子识别的Dox调控的增强型IL13 CAR-T在恶性脑胶质瘤动物模型中的实验治疗研究,2018/01/01-2021/12/31,主要参与人;
5. 国家自然科学基金青年项目,31601086,携带CRISPR/Cas和供体DNA的高容量腺病毒介导的体内细胞高效靶向修饰方法的探究,2017/01-2019/12,18万元,主持;
6. 中央高校基金“自由探索项目”,GK201603113,新型多位点打靶腺病毒载体的构建及研究,2016/01-2017/12,主要参与人;
7. 国家自然科学基金面上项目,81471772,结合靶向基因组编辑技术构建用于单基因缺陷原位修复的新型高容量腺病毒载体,2015/01-2018/12,主要参与人;
8. 国家自然科学基金面上项目,31470058,二酰甘油激酶θ参与非酒精性脂肪肝的发生与缓解过程中的分子机制,2015/01–2016/12,主要参与人;
9. 陕西省自然科学基金,2015JQ8302,二酰甘油激酶DGKθ参与糖、脂代谢调控的分子机制,2015/01–2016/12,主要参与人;
10. 国家自然科学基金面上项目,81272543,骨髓间充质干细胞装载新型药物诱导性溶瘤腺病毒载体Ad5/11-Ind-D24靶向脑胶质母细胞瘤的实验治疗研究,2013/01–2016/12,主要参与人;
11. 中国博士后科学基金面上项目一等资助,2015M570809,用于多位点基因打靶的新型腺病毒载体的构建及应用研究,2015/05-2016/06,主持;
12. 中央高校基金“自由探索项目”,GK201503041,P53和Pten缺失小鼠原位肝癌模型的建立,2015/01-2016/12,主持;
13. 中央高校基本科研业务费创新团队项目,GK201301010,TALEN技术在GUS突变的小鼠模型中的实验治疗研究,2013/01-2015/12,主要参与人;
14. 中央高校基本科研业务费重点项目,GK200901009,锌指酶技术在血友病动物模型中的基因治疗研究,2009/01-2012/12,主要参与人;
15. 陕西省自然科学基金,2007C201,双表达VEGF siRNA 的新型靶向Ad5/3-RGD腺病毒载体在脑胶质母细胞瘤基因治疗中的实验研究,2008/01-2010/12,主要参与人;
四、代表性论文
1. Zhang, W#., Xiao, D#., Li, X., Zhang, Y., Rasouli, J., Casella, G., Boehm, A., Hwang, D., Ishikaw, L.L.W., Thome, R., Ciric, B., Curtis, M., Rostami, A., Zhang, G. X. (2022) SIRT1 inactivation switched astrocytes to an A2-like phenotype in CNS autoimmunity. JCI, doi:10.1172/JCI151803, IF=19.46
2. Rasouli, J., Casella, G., Zhang, W., Xiao D., Kumar, G., Fortina, P., Zhang, G-X., Ciric, B., Rostami, A. (2022) Transcription factor RUNX3 mediates plasticity of ThGM cells toward Th1 phenotype. Front Immunol, 3355, IF=7.97
3. Hwang, D., Seyedsadr, M. S., Ishikawa, L. L. W., Boehm, A., Sahin, Z., Casella, G., Jang, S., Gonzalez, M. V., Garifallou, J. P., Hakonarson, H., Zhang, W., Xiao, D., Rostami, A., Zhang, G. X., Ciric, B. (2022) CSF-1 maintains pathogenic but not homeostatic myeloid cells in the central nervous system during autoimmune neuroinflammation. Proc Natl Acad Sci U S A, 119, e2111804119. IF=12.78
4. Xiao D#, Zhang W#, Wang Q, Li X, Zhang Y, Rasouli J, Casella G, Ciric B, Curtis M, Rostami A, Zhang G-X. (2021) CRISPR-mediated rapid generation of neural cell-specific knockout mice facilitates research in neurophysiology and pathology. Molecular Therapy - Methods & Clinical Development, 20: 755-764. (co-first) IF=5.85
5. Rasouli, J., Casella, G., Ishikawa, L. L. W., Thome, R., Boehm, A., Ertel, A., Melo-Silva, C. R., Mari, E. R., Porazzi, P., Zhang, W., Xiao, D., Sigal, L. J., Fortina, P., Zhang, G. X., Rostami, A.,Ciric, B. (2021) IFN-beta Acts on Monocytes to Ameliorate CNS Autoimmunity by Inhibiting Proinflammatory Cross-Talk Between Monocytes and Th Cells. Front Immunol, 12, 679498. IF=7.97
6. Rasouli, J., Casella, G., Yoshimura, S., Zhang, W., Xiao, D., Garifallou, J., Gonzalez, M.V., Wiedeman, A., Kus, A., Mari, E.R., Fortina, P., Hakonarson, H., Long, S.A., Zhang, G.X., Ciric, B., Rostami, A. (2020) A distinct GM-CSF(+) T helper cell subset requires T-bet to adopt a TH1 phenotype and promote neuroinflammation. Sci Immunol, 5. IF=30.63
7. Li, X., Zhang, Y., Zhang, W., Xiao, D., Ciric, B., Rostami, A., Zhang, G.X. (2020) P7C3 attenuates CNS autoimmunity by inhibiting Th17 cell differentiation. Cell Mol Immunol, 10.1038/s41423-020-0497-5. IF=22.09
8. Casella, G., Rasouli, J., Thome, R., Descamps, H.C., Vattikonda, A., Ishikawa, L., Boehm, A., Hwang, D., Zhang, W., Xiao, D., Park, J., Zhang, G.-X., Alvarez, J.I., Rostami, A., Ciric, B. (2020) Interferon-γ/Interleukin-27 Axis Induces Programmed Death Ligand 1 Expression in Monocyte-Derived Dendritic Cells and Restores Immune Tolerance in Central Nervous System Autoimmunity. Front Immunol, 11, 2425. IF=7.97
9. Casella, G., Rasouli, J., Boehm, A., Zhang, W., Xiao, D., Ishikawa, L.L.W., Thome, R., Li, X., Hwang, D., Porazzi, P., Molugu, S., Tang, H.-Y., Zhang, G.-X., Ciric, B., Rostami, A. (2020) Oligodendrocyte-derived extracellular vesicles as antigen-specific therapy for autoimmune neuroinflammation in mice. Science Translational Medicine, 12, eaba0599. IF=19.32
10. Li, Y., Zhang, W., Zhao, J., Li, S., Shan, L., Zhu, J., Li, Y., Zhu, H., Mao, Q., Xia, H. (2018) Establishing a dual knock-out cell line by lentivirus based combined CRISPR/Cas9 and Loxp/Cre system. Cytotechnology, 70, 1595-1605. IF=2.0
11. Zhang, W., Xiao, D., Shan, L., Zhao, J., Mao, Q., Xia, H. (2017) Generation of apoptosis-resistant HEK293 cells with CRISPR/Cas mediated quadruple gene knockout for improved protein and virus production. Biotechnol Bioeng, 114, 2539-2549. IF=4.5
12. Xiao, D.#, Zhang, W.#, Li, Y., Liu, K., Zhao, J., Sun, X., Shan, L., Mao, Q., Xia, H. (2016) A novel luciferase knock-in reporter system for studying transcriptional regulation of the human Sox2 gene. J Biotechnol, 219, 110-116. (co-first author) IF=3.503
13. Chen, F., Zhang, W., Zhao, J., Yang, P., Ma, R., Xia, H. (2016) [Construction of Rev-erbbeta gene knockout HEK293 cell line with CRISPR/Cas9 system]. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi, 32, 1446-1452.
14. Zhang, W., Wang, D., Liu, S., Zheng, X., Ji, H., Xia, H., Mao, Q. (2014) Multiple copies of a linear donor fragment released in situ from a vector improve the efficiency of zinc-finger nuclease-mediated genome editing. Gene Ther, 21, 282-288. IF=5.2
15. Zhang, W., Chen, H., Zheng, X., Wang, D., Ji, H., Xia, H., Mao, Q. (2014) Targeted genome correction by a single adenoviral vector simultaneously carrying an inducible zinc finger nuclease and a donor template. J Biotechnol, 188, 1-6. IF=3.503
16. Zhang, W., Zheng, X., Wang, Y., Mao, Q., Xia, H. (2012) Establishment of a cell line carrying single copy of an exogenous mutant reporter gene for assaying the biological activity of ZFNs. J Biotechnol, 162, 191-196. IF=3.503
17. Zhang, W., Guo, Y., Zhang, C., Ji, H., Meng, W., Wang, D., Li, X., Mao, Q., Xia, H. (2012) Rescue the failed half-ZFN by a sensitive mammalian cell-based luciferase reporter system. PLoS One, 7, e45169. IF=2.74
18. Li, X., Mao, Q., Wang, D., Zhang, W., Xia, H. (2012) A fiber chimeric CRAd vector Ad5/11-D24 double-armed with TRAIL and arresten for enhanced glioblastoma therapy. Hum Gene Ther, 23, 589-596. IF=5.7
19. Jiang, Y., Liu, J., Zhao, J., Zhang, W., Xia, H. (2010) Eukaryotic expression and identification of human Slit2 gene in HEK-293 cell line. Acta Universitatis Medicinalis Nanjing (Natural Science), 10.3724/SP.J.1238.2010.00512.
20. Liu, S., Mao, Q., Zhang, W., Zheng, X., Bian, Y., Wang, D., Li, H., Chai, L., Zhao, J., Xia, H. (2009) Genetically modified adenoviral vector with the protein transduction domain of Tat improves gene transfer to CAR-deficient cells. Biosci Rep, 29, 103-109. IF=2.942
21. Li, H., Zhang, W., Wang, D., Li, R., Qi, Z., Zhao, J., Xia, H. (2009) [Construction and expression of recombinant adenovirus vector carrying human endostatin, K5 and endostatin-K5 gene]. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi, 25, 577-580.
22. Li, H., Zheng, X., Zhang, W., Bian, Y., Wang, D., Zhao, J., Xia, H. (2007) [Construction of an expression vector for high expression of siRNA]. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi, 23, 1117-1118.
五、授权专利
1. 一种抗凋亡细胞系及其建立方法和应用,2017.03.30-2037.03.29,中国,ZL 2017 10202547.3。
2. 一种基因打靶系统,2015.6.10-2035.6.9,中国,ZL 2013 10157216.4。
3. 锌指蛋白的快速筛选方法,2015.5.27-2035.5.26,中国,ZL 2012 1 0207952.1。
4. 携带锌指核酸酶表达元件和供体DNA的腺病毒及其构建方法和应用,2014.12.10-2034.12.9,中国,ZL 2012 1 0447965.6。
5. 快速检测锌指核酸酶介导基因定点整合的方法,2013.6.12-2033.6.11,中国,ZL 2011 1 0009773.2。
6. 肿瘤特异嵌合启动子及其构建方法和应用,2011.11.30-2031.11.29,中国,ZL 2009 1 0023841.3。
7. 表达小干扰RNA的VA1缺失的腺病毒载体及构建方法和应用,2011.5.4-2031.5.3,中国,ZL 2009 1 0022759.9。