Northeastern Ohio Medical University, Rootstown, OH, USA.
Microb Biotechnol. 2012 Mar;5(2):203-13. doi: 10.1111/j.1751-7915.2011.00278.x. Epub 2011 Sep 6.
The J-LEAPS vaccines contain a peptide from β-2-microglobulin covalently attached to disease-related peptides of 8-30 amino acids which contain a T cell epitope. The J-LEAPS vaccines can initiate a protective Th1 immune response or modulate an ongoing Th17 autoimmune response to the peptide. J-LEAPS vaccines activate and direct the nature of the subsequent immune response by promoting the maturation of precursor cells into a unique type of dendritic cell that produces interleukin 12, but not IL-1 or tumour necrosis factor, and presents the antigenic peptide to T cells. Adoptive transfer of JgD-LEAPS dendritic cells, matured with an anti-HSV-1 vaccine, promoted antigen-specific Th1 protection against lethal challenge with the virus. J-LEAPS peptide immunogens and J-LEAPS dendritic cell vaccines have potential applications for antimicrobial prevention and therapy, treatment of autoimmune diseases, and for cancer immunotherapy.
J-LEAPS 疫苗包含通过共价键连接到含有 T 细胞表位的 8-30 个氨基酸的疾病相关肽的β-2-微球蛋白肽。J-LEAPS 疫苗可以引发保护性 Th1 免疫应答或调节针对肽的进行性 Th17 自身免疫应答。J-LEAPS 疫苗通过促进前体细胞成熟为产生白细胞介素 12(但不产生 IL-1 或肿瘤坏死因子)的独特类型树突状细胞,并将抗原肽呈递给 T 细胞,从而激活和指导随后的免疫应答的性质。用抗单纯疱疹病毒 1 疫苗成熟的 JgD-LEAPS 树突状细胞的过继转移促进了针对病毒致死性攻击的抗原特异性 Th1 保护。J-LEAPS 肽免疫原和 J-LEAPS 树突状细胞疫苗具有用于抗菌预防和治疗、治疗自身免疫性疾病以及癌症免疫治疗的潜在应用。