Elneil Sohier, Lalezari Jacob P, Pourhassan Nader Z
University College London, National Hospital for Neurology and Neurosurgery, London, UK.
Quest Clinical Research, 2300 Sutter Street, Suite #202 & 208, San Francisco, CA, 94115, USA.
J Transl Autoimmun. 2021;4:100097. doi: 10.1016/j.jtauto.2021.100097. Epub 2021 Mar 23.
The number of confirmed cases of infection with SARS-CoV-2, the virus causing Coronavirus disease 2019 (COVID-19), continues to increase and is associated with substantial morbidity and mortality in virtually every country in the world. Although in the long-term mass vaccinations remains the most promising approach to control the pandemic, evidence suggests that new variants of the virus have emerged that may be able to evade the immune responses triggered by current vaccines. Therefore despite the recent approval of a number of SARS-CoV-2 vaccines there remains considerable urgency for effective treatments for COVID-19. Severe-to-critical COVID-19 has been shown to be associated with a dysregulated host immune response to SARS-CoV-2 with elevated levels of C-C chemokine receptor type 5 (CCR5) ligands including chemokine C-C ligands 3, 4, 5, as well as interleukins 6 and 10. Leronlimab, a CCR5-specific humanised IgG4 monoclonal antibody originally developed for the treatment of HIV has been studied for the treatment of COVID-19. In the TEMPEST trial which compared leronlimab to placebo in subjects with mild-to-moderate COVID-19, a analysis showed that leronlimab led to improvements from baseline in National Early Warning Score 2 (NEWS2) at Day 14 in the sub-set of people with more severe disease. Data has also been released on a further ongoing, randomized, placebo-controlled phase 3 registrational trial of leronlimab in 394 people with severe-to-critical COVID-19. The results show that Day 28 mortality was reduced (P = 0.0319) in the subset of participants receiving leronlimab plus other pre-specified commonly used COVID-19 treatments including dexamethasone administered as part of their standard of care (SOC) compared to participants receiving placebo plus other pre-specified commonly used COVID-19 treatments including dexamethasone as part of their SOC. Several cases have recently been reported demonstrated that treatment with leronlimab restores immune function and achieves clinical improvement in people with critical COVID-19. Here we report on a further case of a critically ill person who was treated with leronlimab. This person had been on extracorporeal membrane oxygenation (ECMO) for an extended period of time before receiving 4 doses of leronlimab. The male subject received his first dose of leronlimab on Day 79 of hospitalization he was weaned off ECMO by Day 84 and discharged from the ECMO intensive care unit on Day 91.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)是导致2019冠状病毒病(COVID-19)的病毒,其确诊感染病例数持续增加,几乎在世界上每个国家都造成了大量发病和死亡。虽然从长远来看,大规模接种疫苗仍然是控制疫情最有前景的方法,但有证据表明,该病毒已出现新变种,可能能够逃避当前疫苗引发的免疫反应。因此,尽管最近批准了多种SARS-CoV-2疫苗,但对于COVID-19的有效治疗仍有相当大的紧迫性。重症至危重症COVID-19已被证明与宿主对SARS-CoV-2的免疫反应失调有关,C-C趋化因子受体5(CCR5)配体水平升高,包括趋化因子C-C配体3、4、5,以及白细胞介素6和10。来瑞特莫单抗是一种最初开发用于治疗HIV的CCR5特异性人源化IgG4单克隆抗体,已被研究用于治疗COVID-19。在TEMPEST试验中,将来瑞特莫单抗与安慰剂在轻至中度COVID-19患者中进行比较,一项分析表明,在病情较重的亚组中,来瑞特莫单抗在第14天使国家早期预警评分2(NEWS2)较基线有所改善。关于来瑞特莫单抗在394例重症至危重症COVID-19患者中正在进行的另一项随机、安慰剂对照3期注册试验的数据也已公布。结果显示,与接受安慰剂加其他预先指定的常用COVID-19治疗(包括作为其标准治疗(SOC)一部分给予的地塞米松)的参与者相比,接受来瑞特莫单抗加其他预先指定的常用COVID-19治疗(包括作为其SOC一部分给予的地塞米松)的参与者亚组中,第28天的死亡率降低(P = 0.0319)。最近有几例报告表明,来瑞特莫单抗治疗可恢复重症COVID-19患者的免疫功能并实现临床改善。在此,我们报告另一例接受来瑞特莫单抗治疗的危重症患者。该患者在接受4剂来瑞特莫单抗之前,已长时间使用体外膜肺氧合(ECMO)。该男性患者在住院第79天接受了第一剂来瑞特莫单抗,在第84天停用ECMO,并于第91天从ECMO重症监护病房出院。