Arends Eline J, Meziyerh Soufian, Moes Dirk Jan A R, Kamerling Sylvia W A, van der Kooy Sandra, Ogando Natacha S, Snijder Eric J, van Hemert Martijn, Visser Leo G, Feltkamp Mariet C W, Claas Eric C J, Rabelink Ton J, van Kooten Cees, de Vries Aiko P J, Teng Y K Onno
Department of Internal Medicine section Nephrology, Center of Expertise for Lupus-, Vasculitis and Complement- mediated Systemic Autoimmune Diseases, Leiden University Medical Center, Leiden, the Netherlands.
Department of Internal Medicine section Nephrology, Leiden Transplant Center, Leiden University Medical Center, Leiden, the Netherlands.
Kidney Int Rep. 2023 Sep 7;8(12):2654-2664. doi: 10.1016/j.ekir.2023.09.003. eCollection 2023 Dec.
Immunocompromised kidney patients are at increased risk of prolonged SARS-CoV-2 infection and related complications. Preclinical evidence demonstrates a more potent inhibitory effect of voclosporin on SARS-CoV-2 replication than tacrolimus . We investigated the potential antiviral effects of voclosporin on SARS-CoV-2 in immunocompromised patients.
First, we conducted a prospective, randomized, open-label, proof-of-concept study in 20 kidney transplant recipients (KTRs) on tacrolimus-based immunosuppression who contracted mild to moderate SARS-CoV-2 infection. Patients were randomized to continue tacrolimus or switch to voclosporin. Second, we performed a analysis on SARS-CoV-2 infections in 216 patients with lupus nephritis (LN) on standard immunosuppression who were randomly exposed to voclosporin or placebo as part of a clinical trial that was conducted during the worldwide COVID-19 pandemic.
The primary end point was clearance of SARS-CoV-2 viral load and that did not differ between voclosporin-treated KTRs (median 12 days, interquartile range [IQR] 8-28) and tacrolimus-treated KTRs (median 12 days, IQR 4-16) nor was there a difference in clinical recovery. Pharmacokinetic analyses demonstrated that, when voclosporin trough levels were on-target, SARS-CoV-2 viral load dropped significantly more (ΔCt 7.7 [3.4-10.7]) compared to tacrolimus-treated KTRs (ΔCt 2.7 [2.0-4.3]; = 0.035). In voclosporin-exposed patients with LN, SARS-CoV-2 infection was detected in 6% (7/116) compared to 12% (12/100) in placebo-exposed patients (relative risk [RR] 1.4 [0.97-2.06]). Notably, no voclosporin-exposed patients with LN died from severe SARS-CoV-2 infection compared to 3% (3/100) in placebo-exposed patients (RR 2.2 [1.90-2.54]).
This proof-of-concept study shows a potential positive risk-benefit profile for voclosporin in immunocompromised patients with SARS-CoV-2 infection. These results warrant further investigations on voclosporin to establish an equipoise between infection and maintenance immunosuppression.
免疫功能低下的肾病患者感染严重急性呼吸综合征冠状病毒2(SARS-CoV-2)并出现相关并发症的风险增加。临床前证据表明,与他克莫司相比,voclosporin对SARS-CoV-2复制的抑制作用更强。我们研究了voclosporin对免疫功能低下患者体内SARS-CoV-2的潜在抗病毒作用。
首先,我们对20名接受基于他克莫司免疫抑制治疗且感染轻度至中度SARS-CoV-2的肾移植受者(KTR)进行了一项前瞻性、随机、开放标签的概念验证研究。患者被随机分为继续使用他克莫司或改用voclosporin。其次,我们对216名接受标准免疫抑制治疗的狼疮性肾炎(LN)患者的SARS-CoV-2感染情况进行了分析,这些患者在全球新冠疫情期间作为一项临床试验的一部分被随机给予voclosporin或安慰剂。
主要终点是SARS-CoV-2病毒载量的清除,接受voclosporin治疗的KTR(中位时间12天,四分位间距[IQR]8 - 28)和接受他克莫司治疗的KTR(中位时间12天,IQR 4 - 16)之间无差异,临床恢复情况也无差异。药代动力学分析表明,当voclosporin谷浓度达到目标值时,与接受他克莫司治疗的KTR相比,SARS-CoV-2病毒载量下降幅度更大(ΔCt 7.7 [3.4 - 10.7])(接受他克莫司治疗的KTR的ΔCt为2.7 [2.0 - 4.3];P = 0.035)。在接受voclosporin治疗的LN患者中,6%(7/116)检测到SARS-CoV-2感染,而接受安慰剂治疗的患者中这一比例为12%(12/100)(相对风险[RR] 1.4 [0.97 - 2.06])。值得注意的是,接受voclosporin治疗的LN患者中没有因严重SARS-CoV-2感染死亡的,而接受安慰剂治疗的患者中有3%(3/100)死亡(RR 2.2 [1.90 - 2.54])。
这项概念验证研究表明,voclosporin对于感染SARS-CoV-2的免疫功能低下患者可能具有积极的风险效益比。这些结果值得对voclosporin进行进一步研究,以确定在感染与维持免疫抑制之间的平衡。