Schoot Tessa S, Kerckhoffs Angèle P M, Hilbrands Luuk B, van Marum Rob J
Department of Nephrology, Radboud University Medical Center, Nijmegen, Netherlands.
Department of Nephrology, Jeroen Bosch Hospital, 's-Hertogenbosch, Netherlands.
Front Pharmacol. 2020 Aug 28;11:1333. doi: 10.3389/fphar.2020.01333. eCollection 2020.
Coronavirus disease 2019 (COVID-19) is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It is currently unknown whether immunosuppressive drugs are advantageous or detrimental in patients with COVID-19. Immunosuppressive drugs could be harmful in the initial phase of COVID-19. In this phase, the host immune response is necessary to inhibit viral replication. However, immunosuppressive drugs might have a beneficial effect in the later, more severe phase of COVID-19. In this phase, an overshoot of the host immune response (the "cytokine storm") can cause ARDS, multiorgan failure and mortality.
To summarize the available evidence on the effect of immunosuppressive drugs on infection with SARS-CoV-2. The effects of immunosuppressive drugs on similar pandemic coronaviruses may resemble the effects on SARS-CoV-2. Thus, we also included studies on the severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome coronavirus (MERS-CoV).
The study protocol was registered in PROSPERO (registration number CRD42020181137). We included randomized controlled trials (RCTs), cohort studies with a control group and case-control studies concerning humans ≥ 18 years old. We also included studies and animal studies with a control group.
Sixty-nine studies were included. Interestingly, MPA inhibits SARS-CoV-2 replication . Clinical studies are needed to confirm the inhibitory effect of MPA on SARS-CoV-2 replication . There are indications that corticosteroids and IL-6 inhibitors, like tocilizumab, can reduce mortality and prevent mechanical ventilation in patients with COVID-19. However, observational studies have contradictory results and the risk of bias is high. Thus, these results have to be confirmed in high-quality clinical trials before these drugs can be implemented as standard care. Based on the positive results of CNIs, mTOR inhibitors and thiopurine analogues in studies with SARS-CoV and MERS-CoV, it would be interesting to investigate their effects on SARS-CoV-2 replication.
2019冠状病毒病(COVID-19)由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起。目前尚不清楚免疫抑制药物对COVID-19患者是有益还是有害。免疫抑制药物在COVID-19的初始阶段可能有害。在此阶段,宿主免疫反应对于抑制病毒复制是必要的。然而,免疫抑制药物在COVID-19后期更严重阶段可能具有有益作用。在此阶段,宿主免疫反应过度(“细胞因子风暴”)可导致急性呼吸窘迫综合征、多器官功能衰竭和死亡。
总结免疫抑制药物对SARS-CoV-2感染影响的现有证据。免疫抑制药物对类似大流行冠状病毒的影响可能与对SARS-CoV-2的影响相似。因此,我们还纳入了关于严重急性呼吸综合征冠状病毒(SARS-CoV)和中东呼吸综合征冠状病毒(MERS-CoV)的研究。
研究方案已在国际前瞻性系统评价注册库(PROSPERO)注册(注册号CRD42020181137)。我们纳入了随机对照试验(RCT)、有对照组的队列研究以及针对≥18岁人群的病例对照研究。我们还纳入了有对照组的体外研究和动物研究。
共纳入69项研究。有趣的是,霉酚酸(MPA)可抑制SARS-CoV-2复制。需要进行临床研究以证实MPA对SARS-CoV-2复制的抑制作用。有迹象表明,皮质类固醇和白细胞介素-6抑制剂(如托珠单抗)可降低COVID-19患者的死亡率并预防机械通气。然而,观察性研究结果相互矛盾且偏倚风险较高。因此,在这些药物可作为标准治疗方法实施之前,必须在高质量临床试验中对这些结果进行证实。基于钙调神经磷酸酶抑制剂(CNIs)、雷帕霉素靶蛋白(mTOR)抑制剂和硫嘌呤类似物在SARS-CoV和MERS-CoV体外研究中的阳性结果,研究它们对SARS-CoV-2复制的影响将很有意义。