Department of Nephrology and Medical Intensive Care, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
Department of Infectious Diseases and Respiratory Medicine, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
Transpl Int. 2022 Mar 31;35:10109. doi: 10.3389/ti.2022.10109. eCollection 2022.
Antiviral drugs have shown little impact in patient infected with acute respiratory coronavirus 2 (SARS-CoV-2). Especially for immunocompromised persons positive for SARS-CoV-2, novel treatments are warranted. Recently, the U.S. FDA has granted an emergency use authorization (EUA) to two monoclonal antibodies (mAb) targeting the viral spike protein: bamlanivimab and casivirimab and imdevimab. As per the EUA, all SARS-CoV-2 positive organ transplant recipients can receive mAb treatment. We queried our center's transplant registry to identify SARS-CoV-2 infected recipients treated with single doses of either Bamlanivimab or casivirimab/imdevimab up to May 31, 2021. We analyzed clinical outcomes, renal function and virus-specific antibodies. The co-primary endpoints were hospitalization due to COVID-19 and SARS-CoV-2 RT-PCR negativity. Thirteen patients at a median interval of 55 (IQR, 26-110) months from transplant were treated: 8 with bamlanivimab and 5 with casivirimab/imdevimab. In all, 4/13 (31%) patients were hospitalized at some time, while 11/13 (85%) achieved PCR negativity. 2/4 hospitalized patients received mAb as rescue treatment. Overall mortality was 23%, with one death attributable to transplant-associated lymphoma. All six patients infected with the B 1.1.7 variant were alive at last contact. : mAb treatment appears effective when administered early to SARS-CoV-2-infected transplant recipients.
抗病毒药物在感染急性呼吸道冠状病毒 2(SARS-CoV-2)的患者中效果甚微。对于 SARS-CoV-2 阳性的免疫功能低下者,需要新的治疗方法。最近,美国 FDA 授予了两种针对病毒刺突蛋白的单克隆抗体(mAb)紧急使用授权(EUA):bamlanivimab 和 casivirimab 以及 imdevimab。根据 EUA,所有 SARS-CoV-2 阳性的器官移植受者均可接受 mAb 治疗。我们查询了本中心的移植登记处,以确定截至 2021 年 5 月 31 日,接受单次 Bamlanivimab 或 casivirimab/imdevimab 治疗的 SARS-CoV-2 感染受者。我们分析了临床结局、肾功能和病毒特异性抗体。主要终点是因 COVID-19 住院和 SARS-CoV-2 RT-PCR 阴性。13 名患者在移植后中位数间隔 55 个月(IQR,26-110)接受了治疗:8 名接受 bamlanivimab 治疗,5 名接受 casivirimab/imdevimab 治疗。共有 4/13(31%)的患者曾住院,而 11/13(85%)的患者达到了 PCR 阴性。4 名住院患者中有 2 名接受了 mAb 作为挽救治疗。总体死亡率为 23%,其中 1 例死亡归因于移植相关淋巴瘤。最后一次联系时,所有 6 名感染 B 1.1.7 变异株的患者均存活。:mAb 治疗在 SARS-CoV-2 感染的移植受者早期给药时似乎有效。