School of Cellular and Molecular Medicine, University of Bristol, Medical Sciences Building, University Walk, Bristol, BS8 1TD, UK.
Curr Opin Immunol. 2010 Oct;22(5):609-15. doi: 10.1016/j.coi.2010.08.006. Epub 2010 Sep 17.
Nearly a century has passed since the first report describing antigen-specific immunotherapy (antigen-SIT) was published. Research into the use of antigen-SIT in the treatment of both allergic and autoimmune disease has increased dramatically since, although its mechanism of action is only slowly being unravelled. It is clear though, from recent studies, that success of antigen-SIT depends on the induction of regulatory T (T reg) cell subsets that recognise potentially disease-inducing epitopes. The major challenge remaining for the widespread use of antigen-SIT is to safely administer high doses of immunodominant and potentially pathogenic epitopes in a manner that induces T cell tolerance rather than activation. This review illustrates that intelligent design of treatment agents and strategies can lead to the development of safe and effective antigen-SIT.
自首次报道描述抗原特异性免疫治疗(antigen-SIT)以来,将近一个世纪过去了。此后,针对抗原-SIT 在治疗过敏和自身免疫性疾病中的应用的研究急剧增加,尽管其作用机制仍在缓慢揭示中。然而,从最近的研究中可以清楚地看出,抗原-SIT 的成功取决于诱导能够识别潜在致病表位的调节性 T(Treg)细胞亚群。抗原-SIT 广泛应用的主要挑战仍然是安全地给予免疫优势和潜在致病表位的高剂量,以诱导 T 细胞耐受而不是激活。这篇综述表明,治疗剂和策略的智能设计可以导致安全有效的抗原-SIT 的发展。