中和性单克隆抗体在COVID-19肾移植受者中的应用体会

I. G. Kim, M. Lysenko, N. Frolova, L. Artyukhina, T. Buruleva, A. Nikitina, V. Vinogradov, E. Volodina, V. I. Chervinko, E. Kryukov, M. Zubkin
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引用次数: 0

摘要

在COVID-19暴发期间,对包括肾移植受者在内的严重疾病高风险患者,使用中和性单克隆抗体(mab)治疗尤为重要。目的:评价中和单克隆抗体治疗轻、中度新冠肺炎KTRs的疗效和安全性。材料和方法。这项回顾性研究包括了99名在2021年9月1日至12月31日期间因COVID-19住院治疗的ktr患者。年龄52.0±11.5岁(M, 47.5%)。单抗采用巴兰尼维单抗/依替西维单抗联合用药,剂量为700/1400 mg。为了评估单克隆抗体治疗的疗效,我们确定了两组患者。组1包括33名接受单克隆抗体作为治疗成分之一的ktr患者,而组2包括66名未接受单克隆抗体的患者。出院或死亡被视为随访的终点。在第1组,使用单克隆抗体后,肺过程进展的频率低于对照组,CT1-2转化为CT3-4(分别为9.1%和30.3%,p < 0.01)。1组ktr与2组有显著差异,ICU和呼吸机护理需求降低(分别为6.1% vs. 27.3%和3% vs. 19.8%)。两组在性别、年龄、体重指数、Charlson合并症指数(CCI)和发病时肾移植后时间(KTx)以及住院时的rnseline血液生化参数值方面具有可比性。在病程较晚住院的非单克隆抗体患者中,只有c反应蛋白(CRP)和纤维蛋白原值较高(组1为7.7±3.2天,组1为4.6±1.6天,p < 0.001)。其他治疗的处方频率在对照组之间没有差异。单克隆抗体的使用显著降低了KTRs的死亡率,从第2组的19.7%降至第1组的3%,而对移植物功能没有不良影响。结论。在KTRs的COVID-19早期阶段使用单克隆抗体治疗是安全的,它可以预防严重的COVID-19,并减少不良后果的发生率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Experience in the use of neutralizing monoclonal antibodies in kidney transplant recipients with COVID-19
 Therapy with neutralizing monoclonal antibodies (mAbs) is particularly relevant during COVID-19 outbreaks in patients at high risk of severe disease, including kidney transplant recipients (KTRs).Objective: to evaluate the efficacy and safety of neutralizing mAbs in KTRs with mild to moderate COVID-19.Materials and methods. The retrospective study included 99 KTRs who received inpatient treatment for COVID-19 between September 1 and December 31, 2021. Patients were 52.0 ± 11.5 years old (M, 47.5%). Bamlanivimab/etesevimab combination drug at a dose of 700/1400 mg was used as mAbs. To evaluate the efficacy of mAbs therapy, two groups of patients were identified. Group 1 consisted of 33 KTRs who received mAbs as one of the therapy components, while group 2 consisted of 66 patients who received no mAbs. Discharge from the hospital or death was considered as the endpoint of follow-up.Results. In group 1, after the use of mAb, progression of pulmonary process was observed less frequently than in the control group with CT1-2 transformation to CT3-4 (9.1% vs. 30.3%, respectively, p < 0.01). Group 1 KTRs differed significantly from group 2 - lower need for ICU and ventilator care (6.1% vs. 27.3% and 3% vs. 19.8%, respectively). The groups were comparable by sex, age, body mass index, Charlson Comorbidity Index (CCI) and time after kidney transplant (KTx) at the onset of the disease and by rnseline blood biochemistry parameter values at the time of hospitalization. Only C-reactive protein (CRP) and fibrinogen values were higher in the non-mAbs patients who were hospitalized later in the course of the disease (7.7 ± 3.2 days versus 4.6 ± 1.6 days in group 1, p < 0 .001). The frequency of prescription of other therapies did not differ between the compared groups. Use of mAbs significantly reduced mortality from 19.7% in KTRs in group 2 to 3% in group 1 without adverse effect on graft function. Conclusion. The use of mAbs therapy in the early stages of COVID-19 in KTRs is safe, it prevents severe COVID-19, and reduces the incidence of adverse outcomes.
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