State Key Laboratory for Agro-Biotechnology, College of Biological Science, China Agricultural University, Beijing, China.
J Gene Med. 2009 Nov;11(11):1064-70. doi: 10.1002/jgm.1387.
DNA vaccination is a strategy that has been developed primarily to elicit protective immunity against infection and cancer.
DNA vaccine was used, in conjunction with an immunosuppressant, to tolerize harmful autoimmunity.
Immunization of C57BL/6 mice with MOG(35-55), a myelin oligodendrocyte glycoprotein-derived peptide, and FK506 (Tacrolimus) as a tolerogenic adjuvant stimulated regulatory dendritic cells, induced antigen-specific regulatory T cells (Treg), and protected the animals from subsequent induction of experimental autoimmune encephalomyelitis (EAE). After EAE induction, there were fewer lymphocytes, including fewer T helper 17 cells, and more Treg infiltrating the spinal cord in the immunized mice compared to in control mice. Furthermore, at the peak of the EAE manifestation, CD4 T cells in the immunized mice showed decreased expression of interferon-gamma and interleukin (IL)-17, but not IL-4, in treated mice.
DNA vaccination, when applied with an immunosuppressant as adjuvant, can induce antigen-specific tolerance and prevent autoimmune disease.
DNA 疫苗主要是为了激发针对感染和癌症的保护性免疫而开发的一种策略。
使用 DNA 疫苗联合免疫抑制剂来耐受自身免疫的有害性。
用髓鞘少突胶质细胞糖蛋白衍生肽 MOG(35-55)和作为耐受佐剂的 FK506(他克莫司)对 C57BL/6 小鼠进行免疫接种,刺激了调节性树突细胞,诱导了抗原特异性调节性 T 细胞(Treg),并保护动物免受随后实验性自身免疫性脑脊髓炎(EAE)的诱导。在 EAE 诱导后,与对照组小鼠相比,免疫小鼠的脊髓中浸润的淋巴细胞(包括 Th17 细胞)减少,Treg 增加。此外,在 EAE 表现的高峰期,与未处理组相比,免疫组小鼠的 CD4 T 细胞中干扰素-γ和白细胞介素(IL)-17 的表达降低,但 IL-4 表达没有降低。
当与免疫抑制剂作为佐剂一起应用时,DNA 疫苗可以诱导抗原特异性耐受并预防自身免疫性疾病。