Salama Alan D
UCL Department of Renal Medicine, Royal Free Hospital, London, United Kingdom.
Kidney Int Rep. 2019 Oct 24;5(1):7-12. doi: 10.1016/j.ekir.2019.10.005. eCollection 2020 Jan.
Clinical relapses are common in anti-neutrophil cytoplasm antibody (ANCA)-associated vasculitis, necessitating repeated treatment with immunosuppressive therapy, and increasing the risks of severe adverse events. Better understanding the basis of relapse would help stratify patients, testing the notion that more treatment may prevent development of relapse, whereas in those at low risk of disease flares, treatment minimization may be appropriate, reducing risks of adverse events, most notably infectious complications and drug toxicity. However, relapse can only occur following remission, and although defining clinical remission may seem straightforward, there is evidence in many remission patients of persistent inflammatory and immunological activity, at levels above those found in healthy individuals. This suggests that we may not truly be achieving disease remission in many patients and these persistent responses may set the patient up for subsequent disease flares. Understanding the underlying pathophysiological basis of disease activity and remission is paramount to help define better biomarkers of relapse, which should positively affect adverse events and patient outcomes.
临床复发在抗中性粒细胞胞浆抗体(ANCA)相关血管炎中很常见,这就需要反复使用免疫抑制疗法进行治疗,并增加了严重不良事件的风险。更好地理解复发的基础将有助于对患者进行分层,验证更多治疗可能预防复发的观点,而对于疾病发作风险较低的患者,尽量减少治疗可能是合适的,这样可以降低不良事件的风险,尤其是感染并发症和药物毒性。然而,复发只能在缓解后发生,虽然定义临床缓解看似简单,但有证据表明,许多处于缓解期的患者存在持续的炎症和免疫活动,其水平高于健康个体。这表明我们可能并未在许多患者中真正实现疾病缓解,而这些持续的反应可能使患者易于随后出现疾病发作。了解疾病活动和缓解的潜在病理生理基础对于帮助定义更好的复发生物标志物至关重要,这应该会对不良事件和患者预后产生积极影响。