Department of Medical Genetics, "Iuliu Hațieganu" University of Medicine and Pharmacy, Str. Pasteur nr. 6, 400349, Cluj-Napoca, Romania; Department of Internal Medicine, Radboud University Medical Center, Nijmegen, Geert Grooteplein Zuid 8, 6525 GA, Nijmegen, The Netherlands; Radboud Institute of Molecular Life Sciences (RIMLS), Radboud University Medical Center, Geert Grooteplein Zuid 28, 6525 GA, Nijmegen, The Netherlands.
Department of Medical Genetics, "Iuliu Hațieganu" University of Medicine and Pharmacy, Str. Pasteur nr. 6, 400349, Cluj-Napoca, Romania.
Joint Bone Spine. 2022 Jul;89(4):105364. doi: 10.1016/j.jbspin.2022.105364. Epub 2022 Feb 24.
Rheumatic diseases include a variety of autoimmune and autoinflammatory conditions that are characterised by musculoskeletal involvement and systemic disease. Both innate and adaptive immunity can contribute to the complex inflammatory processes that take part in the pathogenesis of these debilitating disorders.
Over the past decade, studies have led to a paradigm-shift around the concept of immune memory, generating the knowledge that cells of the innate immune system can develop a de facto memory mediated by epigenetic reprograming and metabolic changes (trained immunity). Here we provide an overview of current data that describe features of trained immunity in rheumatic diseases. We link evidence on inflammatory mediators and cytokine production, immunometabolism and epigenetic regulation of immunological programs, and outline the fact that trained immunity could play mechanistic roles in rheumatic diseases such as gout, rheumatoid arthritis, systemic lupus erythematosus or systemic sclerosis.
This review describes recent findings in several important rheumatic disorders and emphasizes changes in the functional program of innate immune cells that are reminiscent of a trained immune phenotype. Further assessment of trained immunity in rheumatic disease can provide targetable mechanisms that could potentially alter the disease symptomatology and evolution.
风湿性疾病包括多种自身免疫和自身炎症性疾病,其特征为肌肉骨骼受累和全身疾病。先天免疫和适应性免疫均可导致参与这些使人衰弱的疾病发病机制的复杂炎症过程。
在过去的十年中,研究围绕免疫记忆的概念发生了转变,产生了先天免疫系统的细胞可以通过表观遗传重编程和代谢变化(训练有素的免疫)介导事实上的记忆的知识。在这里,我们概述了目前描述风湿性疾病中训练有素的免疫特征的现有数据。我们将炎症介质和细胞因子产生、免疫代谢和免疫程序的表观遗传调控方面的证据联系起来,并概述了这样一个事实,即训练有素的免疫可能在痛风、类风湿关节炎、系统性红斑狼疮或系统性硬化症等风湿性疾病中发挥机制作用。
本综述描述了几种重要风湿性疾病的最新发现,并强调了先天免疫细胞功能程序的变化,这些变化使人联想到训练有素的免疫表型。进一步评估风湿性疾病中的训练有素免疫可以提供潜在改变疾病症状和演变的靶向机制。