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Rheumatoid arthritis vaccine therapies: perspectives and lessons from therapeutic ligand epitope antigen presentation system vaccines for models of rheumatoid arthritis

机译:类风湿关节炎疫苗疗法:类风湿关节炎模型的治疗性配体表位抗原呈递系统疫苗的观点和教训

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摘要

The current status of therapeutic vaccines for autoimmune diseases is reviewed with rheumatoid arthritis as the focus. Therapeutic vaccines for autoimmune diseases must regulate or subdue responses to common self-antigens. Ideally, such a vaccine would initiate an antigen-specific modulation of the T-cell immune response that drives the inflammatory disease. Appropriate animal models and types of T helper cells and signature cytokine responses that drive autoimmune disease are also discussed. Interpretation of these animal models must be done cautiously because the means of initiation, autoantigens, and even the signature cytokine and T helper cell (Th1 or Th17) responses that are involved in the disease may differ significantly from those in humans. We describe ligand epitope antigen presentation system vaccine modulation of T-cell autoimmune responses as a strategy for the design of therapeutic vaccines for rheumatoid arthritis, which may also be effective in other autoimmune conditions.
机译:以类风湿性关节炎为重点,综述了自身免疫性疾病治疗疫苗的现状。自身免疫性疾病的治疗性疫苗必须调节或抑制对常见自身抗原的反应。理想地,这样的疫苗将引发驱动炎性疾病的T细胞免疫应答的抗原特异性调节。还讨论了适当的动物模型和辅助性T细胞的类型以及驱动自身免疫性疾病的标志性细胞因子反应。必须谨慎进行这些动物模型的解释,因为该疾病涉及的起始方式,自身抗原,甚至特征性细胞因子和T辅助细胞(Th1或Th17)应答可能与人类的应答明显不同。我们描述了配体抗原决定簇抗原呈递系统疫苗调节T细胞自身免疫反应作为类风湿关节炎治疗性疫苗设计策略,在其他自身免疫性疾病中也可能有效。

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