Zarei Shohreh, Arrighi Jean-François, Ongaro Gioele, Calzascia Thomas, Haller Olivier, Frossard Christophe, Piguet Vincent, Walker Paul R, Hauser Conrad
Allergy Unit, Division of Immunology and Allergy, University Hospital, Geneva Switzerland.
J Invest Dermatol. 2003 Oct;121(4):745-50. doi: 10.1046/j.1523-1747.2003.12492.x.
Dendritic cells are excellent targets for antigen-specific immune intervention. Here we attempted to introduce a CD8 T cell-dependent epitope into dendritic cells for presentation on major histocompatibility complex class I and induction of immunity. Murine bone-marrow-derived dendritic cells were subjected to electroporation with mRNA transcribed in vitro from a plasmid encoding lymphocytic choriomeningitis virus glycoprotein or enhanced green fluorescent protein under the control of a T7 promotor. The transfection efficiency of dendritic cells was 22 to 40%. Maturation was not inhibited by the electroporation. Dendritic cells electroporated with the appropriate antigen induced cell number-dependent in vitro proliferation in CD8 T cells expressing a transgenic receptor recognizing the 33 to 41 sequence of lymphocytic choriomeningitis virus glycoprotein in association with H-2Kb/Db, indicating correct synthesis, processing, and presentation of the epitope. Naive C57BL/6 mice vaccinated with electroporated dendritic cells and challenged with lymphocytic choriomeningitis virus were protected. Vaccination induced epitope-specific T cells as assessed by tetramer staining in blood and spleen. These results indicate that targeting dendritic cells with antigen-encoding mRNA can induce antigen-specific CD8 T cell responses as well as protective anti-viral immunity in vivo. Targeting dendritic cells with antigen-encoding mRNA may find wider application for immune intervention in disorders such as autoimmunity and cancer.
树突状细胞是抗原特异性免疫干预的理想靶点。在此,我们尝试将一个依赖CD8 T细胞的表位导入树突状细胞,以便在主要组织相容性复合体I类分子上呈递并诱导免疫反应。用在T7启动子控制下从编码淋巴细胞脉络丛脑膜炎病毒糖蛋白或增强型绿色荧光蛋白的质粒体外转录的mRNA对小鼠骨髓来源的树突状细胞进行电穿孔。树突状细胞的转染效率为22%至40%。电穿孔未抑制其成熟。用适当抗原进行电穿孔的树突状细胞在表达识别与H-2Kb/Db相关的淋巴细胞脉络丛脑膜炎病毒糖蛋白33至41序列的转基因受体的CD8 T细胞中诱导了细胞数量依赖性的体外增殖,表明表位的正确合成、加工和呈递。接种电穿孔树突状细胞并受到淋巴细胞脉络丛脑膜炎病毒攻击的未免疫C57BL/6小鼠受到了保护。通过血液和脾脏中的四聚体染色评估,疫苗接种诱导了表位特异性T细胞。这些结果表明,用编码抗原的mRNA靶向树突状细胞可在体内诱导抗原特异性CD8 T细胞反应以及保护性抗病毒免疫。用编码抗原的mRNA靶向树突状细胞可能在自身免疫和癌症等疾病的免疫干预中得到更广泛的应用。