MS Center and Unit of Neuroimmunology, Department of Neurology, Hadassah Medical Center, Jerusalem, Israel.
Immunol Res. 2018 Dec;66(6):642-648. doi: 10.1007/s12026-018-9032-5.
Immunotherapy of multiple sclerosis (MS) and other neuroimmune diseases is rapidly evolving. For the past 25 years, there has been an accelerating inclusion of new immunomodulating drugs. Based on their molecular construction and their basic mechanism of action, immunotherapeutic agents belong to the following categories: (1) cytotoxic drugs, (2) synthetic immunomodulators, (3) monoclonal antibodies, (4) vaccines (T cell vaccines, antigen vaccines), (5) oral tolerizing agents, (6) modalities that act as indirect immunosuppressants (plasmapheresis, intravenous immunoglobulins [IVIG]), and (7) cellular therapies. MS immunotherapies may also be classified in a different way, into treatments that are given continuously (chronic treatments) and medications that are applied intermittently (IRTs). The principle behind the latter is depletion of the immune system that allows it to rebuild itself. Upon its reconstitution/resetting, the immune system regains the ability to respond to infections and survey the periphery for cancer. An IRT by definition is given at short intermittent courses and not continuously. IRT modalities were shown to induce long-term remission of MS that, in some cases, is close to the definition of a "cure." There are cohorts of patients having been treated with the IRTs, alemtuzumab, and HSCT, who experience-under these modalities-no evidence of disease activity (NEDA) for over 10 years. Most importantly, IRTs cause radical changes in the lymphocyte repertoire after the reconstitution phase that may explain the long-term beneficial effects of IRT and the possibility of re-induction of self-tolerance to self/myelin antigens. In comparison, a chronic treatment cannot result in cure of the autoimmune reactivity, because it only blocks the immune system, as long as it is given; it cannot therefore radically affect the immunopathogenesis of the disease. The risks of adverse events related to immune suppression (such as opportunistic infections and secondary malignancies) with IRTs are lower and front-loaded, whereas the common side effects of chronic immunomodulation are higher and accumulate with time. In conclusion, IRT provides a novel concept for MS therapy with substantial advantages over chronic immunosuppression. IRT therapies have shown a significantly higher level of efficacy in MS. The "Holy grail" of the treatment of autoimmunity, which is to re-induce the disrupted self-tolerance, seems to be achievable-at least in part-with this approach. Moreover, the benefits of IRT, administered in short pulses, include significantly higher adherence to treatment and lower risks for accumulative side effects that are typically associated with chronic immunosuppression.
多发性硬化症(MS)和其他神经免疫疾病的免疫治疗正在迅速发展。在过去的 25 年中,新型免疫调节药物的应用不断加速。根据其分子结构和基本作用机制,免疫治疗药物可分为以下几类:(1)细胞毒性药物,(2)合成免疫调节剂,(3)单克隆抗体,(4)疫苗(T 细胞疫苗、抗原疫苗),(5)口服耐受药物,(6)作为间接免疫抑制剂的方法(血浆置换、静脉注射免疫球蛋白[IVIG]),以及(7)细胞疗法。MS 免疫疗法也可以通过不同的方式进行分类,分为持续给药的治疗方法(慢性治疗)和间歇性给药的药物(IRTs)。后者的原理是耗尽免疫系统,使其能够重建自身。在重建/重置后,免疫系统能够重新响应感染并监测外周组织中的癌症。IRT 定义为短时间的间歇性疗程,而不是持续给药。IRT 模式已被证明可诱导 MS 的长期缓解,在某些情况下,接近“治愈”的定义。有一批接受 IRT、阿仑单抗和 HSCT 治疗的患者,在这些治疗模式下,超过 10 年没有疾病活动的证据(NEDA)。最重要的是,在重建阶段后,IRT 会导致淋巴细胞谱发生根本性变化,这可能解释了 IRT 的长期有益效果以及重新诱导自身/髓鞘抗原自身耐受性的可能性。相比之下,慢性治疗不能治愈自身免疫反应,因为只要给予治疗,它就只能阻断免疫系统;因此,它不能从根本上影响疾病的免疫发病机制。与 IRT 相关的免疫抑制相关不良事件(如机会性感染和继发性恶性肿瘤)的风险较低,并且在前载时较高,而慢性免疫调节的常见副作用较高,并随时间积累。总之,IRT 为 MS 治疗提供了一种新的概念,与慢性免疫抑制相比具有显著优势。IRT 疗法在 MS 中的疗效明显更高。通过这种方法,似乎至少部分可以实现自身免疫治疗的“圣杯”,即重新诱导中断的自身耐受性。此外,在短脉冲中给予 IRT 的益处包括更高的治疗依从性和更低的累积副作用风险,而这些副作用通常与慢性免疫抑制有关。