Stanway James A, Isaacs John D
National Institute for Health Research, Northern Deanery, Newcastle upon Tyne, UK; Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK; Musculoskeletal Unit, Newcastle upon Tyne Hospitals National Health Service Foundation Trust, Newcastle upon Tyne, UK.
Lancet Rheumatol. 2020 Sep;2(9):e565-e575. doi: 10.1016/S2665-9913(20)30100-4. Epub 2020 Aug 26.
Autoimmunity is currently managed with generalised immunosuppression, which is associated with serious side-effects such as infection and cancer. An ideal treatment strategy would be to induce immune tolerance-ie, to reprogramme the immune system to stop recognising the host itself as a threat. Drug-free remission should follow such an intervention, representing a change in the approach to the treatment of autoimmune disease. Tolerance induction is achievable in animal models of autoimmunity but translation to the clinic has been slow. Nonetheless, progress has been made-eg, restoration of therapeutic responsiveness and drug-free remission have been achieved with stem cell transplantation in refractory autoimmunity, and significant delays in onset of type 1 diabetes in individuals at high risk have been achieved following a brief treatment with anti-CD3 monoclonal antibody. In the future, antigen-specific interventions should provide highly targeted, personalised approaches, avoiding generalised immunosuppression entirely. Such trials have already started, using both direct autoantigenic peptide administration, cellular therapies, and other modalities. In this Series paper, we discuss the history of immune tolerance induction with a focus on rheumatological disease while also highlighting essential data from other specialties. We propose key unanswered questions, which will be covered in other papers in this Series.
目前,自身免疫性疾病通过全身性免疫抑制进行治疗,这会带来诸如感染和癌症等严重副作用。理想的治疗策略应该是诱导免疫耐受,即重新编程免疫系统,使其不再将宿主自身视为威胁。这种干预之后应能实现无药物缓解,这代表了自身免疫性疾病治疗方法的一种转变。在自身免疫性疾病的动物模型中可以实现耐受诱导,但向临床的转化进展缓慢。尽管如此,还是取得了一些进展,例如在难治性自身免疫性疾病中通过干细胞移植实现了治疗反应性的恢复和无药物缓解,并且在高危个体中,使用抗CD3单克隆抗体进行短暂治疗后,1型糖尿病的发病出现了显著延迟。未来,抗原特异性干预措施应能提供高度靶向、个性化的方法,完全避免全身性免疫抑制。此类试验已经开始,采用了直接给予自身抗原肽、细胞疗法及其他方式。在本系列论文中,我们将讨论免疫耐受诱导的历史,重点关注风湿性疾病,同时也会突出其他专业的重要数据。我们提出了一些关键的未解决问题,本系列的其他论文将对此进行探讨。