Università Vita-Salute San Raffaele, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Unit of Immunology, Rheumatology, Allergy and Rare Diseases (Unirar), IRCCS San Raffaele Scientific Institute, ss Milan, Italy.
Expert Rev Clin Immunol. 2021 May;17(5):471-483. doi: 10.1080/1744666X.2021.1902310. Epub 2021 Mar 25.
Awareness of IgG4-related disease (IgG4-RD) is increasing worldwide and specialists are now familiar with most of its clinical manifestations and mimickers. IgG4-RD promptly responds to glucocorticoids and repeated courses are typically used to induce and maintain remission because the disease relapses in most patients. If left untreated, it can lead to organ dysfunction, organ failure and death. Advancement in our understanding of IgG4-RD pathogenesis is leading to the identification of novel therapeutic targets and emerging treatments are now setting the stage for personalized therapies for the future.
This review focuses on emerging treatment options for IgG4-RD based on our advancing understanding of disease pathophysiology. Research was performed in the English literature on Pubmed and clinicaltrials.gov databases.
Glucocorticoids remain the first-line induction treatment for the multi-organ manifestations of IgG4-RD. Alternative immunosuppressive agents for maintaining remission are warranted in order to avoid long-term steroid toxicity, and to offer a more mechanistic and personalized therapeutic strategy. Targeting B and T-lymphocyte activation represents the most promising approach, but randomized controlled trials are eagerly awaited to confirm positive preliminary experiences reported in case series and small cohort studies.
IgG4 相关疾病(IgG4-RD)在全球范围内的认知度不断提高,专家们现在已经熟悉其大多数临床表现和类似疾病。IgG4-RD 对糖皮质激素反应迅速,通常会使用多次疗程来诱导和维持缓解,因为大多数患者的疾病会复发。如果不治疗,它可能导致器官功能障碍、器官衰竭和死亡。对 IgG4-RD 发病机制的认识不断提高,导致了新的治疗靶点的确定,新兴的治疗方法正在为未来的个性化治疗奠定基础。
本综述基于我们对疾病病理生理学的理解,重点介绍了 IgG4-RD 的新兴治疗选择。在 Pubmed 和 clinicaltrials.gov 数据库中,用英语文献进行了研究。
糖皮质激素仍然是 IgG4-RD 多器官表现的一线诱导治疗药物。为了避免长期使用类固醇的毒性,并提供更具机制性和个性化的治疗策略,有必要寻找维持缓解的替代免疫抑制剂。靶向 B 和 T 淋巴细胞激活是最有前途的方法,但迫切需要随机对照试验来证实病例系列和小队列研究中报告的初步积极经验。