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首页> 外文期刊>Investigative ophthalmology & visual science >Suppression of Murine Experimental Autoimmune Optic Neuritis by Mature Dendritic Cells Transfected with Calcitonin Genea??Related Peptide Gene
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Suppression of Murine Experimental Autoimmune Optic Neuritis by Mature Dendritic Cells Transfected with Calcitonin Genea??Related Peptide Gene

机译:降钙素基因相关肽基因转染成熟树突状细胞对小鼠实验性自身免疫性视神经炎的抑制作用

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Purpose.: Calcitonin gene-related peptide (CGRP) exhibits prominent anti-inflammatory actions. We examined whether CGRP-transfected dendritic cells (DC) prevent the development of experimental autoimmune optic neuritis (EAON) and experimental autoimmune encephalomyelitis (EAE). Methods.: A human CGRP-expressing plasmid was constructed, and used to transfect C57BL/6 mouse bone marrowa??derived matured DC (mDC) by electroporation methods. Transfection efficiency was 50% with 80% cell viability. C57BL/6 mice were immunized with myelo-oligodendrocyte glycoprotein 35-55, and injected intravenously with CGRP-expressing mDC (CGRP gene-transfected group) or mock-transfected mDC (mock-transfected group) at the induction or effector phase. EAE was diagnosed clinically and EAON was assessed histopathologically. Delayed hypersensitivity was measured. Supernatants of spleen cell cultures were assayed for cytokines using ELISA. The CD4 + CD25+Foxp3+ fraction in spleen cells was analyzed using flow cytometry. Results.: For gene therapy in the induction phase, EAE developed in 50% of mice in the CGRP-transfected group compared with 80% in the mock-transfected group, and the mean pathological score for EAON was 1 in the CGRP-transfected group compared with 2 in the mock-transfected group (P 0.05). For gene therapy in the effector phase, the mean EAE clinical score (1.5 vs. 3.0) and mean EAON pathological score (1.0 vs. 2.0) were both lower in the CGRP-transfected group compared with the mock-transfected group (P 0.05). Delayed hypersensitivity was suppressed significantly in the CGRP-transfected group. IL-10 production by spleen cells in the CGRP-transfected group increased independent of MOG concentration, compared with the mock-transfected group. Interestingly, the proportion of CD4 + CD25+Foxp3+ cells increased significantly (P 0.05) in the CGRP-transfected group compared with the mock-transfected group. Conclusions.: Gene therapy with CGRP-expressing mDC was effective in suppressing the development of EAON and EAE.
机译:目的:降钙素基因相关肽(CGRP)表现出突出的抗炎作用。我们检查了CGRP转染的树突状细胞(DC)是否阻止实验性自身免疫性视神经炎(EAON)和实验性自身免疫性脑脊髓炎(EAE)的发展。方法:构建表达人CGRP的质粒,并通过电穿孔法转染C57BL / 6小鼠骨髓来源的成熟DC(mDC)。转染效率为50%,细胞活力为80%。用骨髓少突胶质细胞糖蛋白35-55免疫C57BL / 6小鼠,并在诱导或效应期静脉注射表达CGRP的mDC(CGRP基因转染组)或模拟转染的mDC(模拟转染组)。临床诊断为EAE,组织病理学评估为EAON。测量迟发型超敏反应。使用ELISA测定脾细胞培养物的上清液中的细胞因子。使用流式细胞仪分析脾细胞中的CD4 + CD25 + Foxp3 +组分。结果:在诱导期的基因治疗中,CGRP转染组中50%的小鼠出现了EAE,而模拟转染组中的80%出现了EAE,而CGRP转染组中EAON的平均病理评分为1相比,模拟转染组为2(P <0.05)。对于效应子阶段的基因治疗,与模拟转染组相比,CGRP转染组的平均EAE临床评分(1.5 vs. 3.0)和平均EAON病理评分(1.0 vs. 2.0)均较低(P <0.05 )。在CGRP转染组中,迟发型超敏反应被显着抑制。与模拟转染组相比,CGRP转染组中脾细胞的IL-10产量增加而与MOG浓度无关。有趣的是,与模拟转染组相比,CGRP转染组中CD4 + CD25 + Foxp3 +细胞的比例显着增加(P <0.05)。结论:表达CGRP的mDC基因疗法可有效抑制EAON和EAE的发生。

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