Fiocchi Claudio
Department of Gastroenterology and Hepatology, Digestive Disease Institute, The Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.
Acta Gastroenterol Belg. 2011 Dec;74(4):548-52.
Immune mediated inflammatory diseases (IMIDs) are life long conditions that cause substantial morbidity and disability. Though increasingly common and intensely studied, the cellular and molecular mechanisms underlying their pathogenesis are still unclear. Despite this incomplete knowledge, it is becoming increasingly evident that IMIDs evolve over time, not only from a clinical perspective but also a pathophysiological one. Evidence is accumulating that the events responsible for inflammation and damage in the target organs are not necessarily the same during the evolution of the IMID, and that the immune response evolves in parallel with the clinical manifestations. This has crucial implications for therapy because immunomodulatory interventions aimed at early pathogenic events may no longer be effective when these events have changed due to a different composition of the immune response. Therefore, it is crucial to better understand why and how the IMID associated immune abnormalities evolve over time, so that time-dependent therapies may be rationally implemented for an improved clinical outcome.
免疫介导的炎症性疾病(IMIDs)是一种会导致严重发病和残疾的终身疾病。尽管这类疾病越来越常见且受到广泛研究,但其发病机制的细胞和分子机制仍不清楚。尽管存在这一知识空白,但越来越明显的是,IMIDs不仅从临床角度,而且从病理生理学角度来看,都会随时间演变。越来越多的证据表明,在IMID的演变过程中,导致靶器官炎症和损伤的事件不一定相同,而且免疫反应与临床表现平行演变。这对治疗具有至关重要的意义,因为当由于免疫反应的不同组成导致早期致病事件发生变化时,针对这些事件的免疫调节干预可能不再有效。因此,至关重要的是要更好地理解IMID相关免疫异常随时间演变的原因和方式,以便能够合理实施依赖时间的治疗方法,从而改善临床结果。