Graduate School, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, People's Republic of China.
Vaccine. 2013 Aug 28;31(38):4063-8. doi: 10.1016/j.vaccine.2013.06.101. Epub 2013 Jul 8.
Local overexpression of tumor necrosis factors alpha (TNF-α) is critically involved in the inflammatory response and tissue destruction of rheumatoid arthritis (RA). Currently, the blockade of TNF-α by passive immunotherapy is indeed efficacious in the treatment of RA, but it still present some disadvantages. Induction of high level of anti-TNF-α neutralizing autoantibodies by TNF-α autovaccine has been developed to avoid these shortcomings. This review is to briefly introduce several vaccination approaches that have been used to induce a B cell response, including coupled TNF-α (entire/peptide) with a carrier protein, modified TNF-α with foreign Th cell epitopes, and engineered DNA vaccine. These methods showed remarkable therapeutic efficiency in experimental animals which indicated that active TNF-α immunization would be a promising and cost-effective new treatment option for RA.
肿瘤坏死因子-α(TNF-α)的局部过表达在类风湿关节炎(RA)的炎症反应和组织破坏中起着关键作用。目前,通过被动免疫疗法阻断 TNF-α 确实在 RA 的治疗中有效,但仍存在一些缺点。通过 TNF-α 自身疫苗诱导高水平的抗 TNF-α 中和自身抗体已被开发出来以避免这些缺点。本文简要介绍了几种用于诱导 B 细胞反应的接种方法,包括与载体蛋白偶联的 TNF-α(全长/肽)、带有外源 Th 细胞表位的修饰 TNF-α和工程化 DNA 疫苗。这些方法在实验动物中显示出显著的治疗效果,这表明主动 TNF-α免疫接种将是一种有前途且具有成本效益的 RA 新治疗选择。