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本文引用的文献

1
Association Between AZD7442 (Tixagevimab-Cilgavimab) Administration and Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection, Hospitalization, and Mortality.AZD7442(替沙格韦单抗-西加韦单抗)给药与严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染、住院和死亡的关联。
Clin Infect Dis. 2023 Feb 8;76(3):e126-e132. doi: 10.1093/cid/ciac625.
2
COVID-19 morbidity decreases with tixagevimab-cilgavimab preexposure prophylaxis in kidney transplant recipient nonresponders or low-vaccine responders.在肾移植受者无应答者或低疫苗应答者中,替沙格韦单抗-西加韦单抗暴露前预防可降低COVID-19发病率。
Kidney Int. 2022 Oct;102(4):936-938. doi: 10.1016/j.kint.2022.07.008. Epub 2022 Jul 20.
3
Characterization of Early-Onset Severe Acute Respiratory Syndrome Coronavirus 2 Infection in Immunocompromised Patients Who Received Tixagevimab-Cilgavimab Prophylaxis.接受替沙格韦单抗-西加韦单抗预防的免疫功能低下患者中早发性严重急性呼吸综合征冠状病毒2感染的特征
Open Forum Infect Dis. 2022 Jun 7;9(7):ofac283. doi: 10.1093/ofid/ofac283. eCollection 2022 Jul.
4
Factors Associated with Severe Outcomes Among Immunocompromised Adults Hospitalized for COVID-19 - COVID-NET, 10 States, March 2020-February 2022.与 COVID-19 住院免疫功能低下成年人严重结局相关的因素 - COVID-NET,10 个州,2020 年 3 月-2022 年 2 月。
MMWR Morb Mortal Wkly Rep. 2022 Jul 8;71(27):878-884. doi: 10.15585/mmwr.mm7127a3.
5
Tixagevimab/cilgavimab pre-exposure prophylaxis is associated with lower breakthrough infection risk in vaccinated solid organ transplant recipients during the omicron wave.替沙格韦单抗/西加韦单抗用于暴露前预防,可降低奥密克戎变异株流行期间接受疫苗接种的实体器官移植受者突破性感染的风险。
Am J Transplant. 2022 Dec;22(12):3130-3136. doi: 10.1111/ajt.17128. Epub 2022 Jul 1.
6
Tixagevimab + Cilgavimab: First Approval.替沙格韦单抗+西加韦单抗:首次批准。
Drugs. 2022 Jun;82(9):1001-1010. doi: 10.1007/s40265-022-01731-1.
7
Breakthrough COVID-19 cases despite prophylaxis with 150 mg of tixagevimab and 150 mg of cilgavimab in kidney transplant recipients.尽管在肾移植受者中使用 150 毫克替沙格韦单抗和 150 毫克西加韦单抗进行预防,还是出现了突破性 COVID-19 病例。
Am J Transplant. 2022 Nov;22(11):2675-2681. doi: 10.1111/ajt.17121. Epub 2022 Jun 30.
8
Efficacy and safety of intramuscular administration of tixagevimab-cilgavimab for early outpatient treatment of COVID-19 (TACKLE): a phase 3, randomised, double-blind, placebo-controlled trial.替沙格韦单抗-西加韦单抗肌内注射用于 COVID-19 早期门诊治疗的疗效和安全性(TACKLE):一项 3 期、随机、双盲、安慰剂对照试验。
Lancet Respir Med. 2022 Oct;10(10):985-996. doi: 10.1016/S2213-2600(22)00180-1. Epub 2022 Jun 7.
9
Activity of AZD7442 (tixagevimab-cilgavimab) against Omicron SARS-CoV-2 in patients with hematologic malignancies.AZD7442(替沙格韦单抗-西加韦单抗)对血液系统恶性肿瘤患者中奥密克戎SARS-CoV-2的活性。
Cancer Cell. 2022 Jun 13;40(6):590-591. doi: 10.1016/j.ccell.2022.05.007. Epub 2022 May 16.
10
Intramuscular AZD7442 (Tixagevimab-Cilgavimab) for Prevention of Covid-19.肌肉注射 AZD7442(替沙格韦单抗-西加韦单抗)预防新冠病毒感染。
N Engl J Med. 2022 Jun 9;386(23):2188-2200. doi: 10.1056/NEJMoa2116620. Epub 2022 Apr 20.

高风险患者使用替沙格韦单抗-西加韦单抗(Evusheld)预防 COVID-19:大型学术中心的真实世界经验。

The Prevention of COVID-19 in High-Risk Patients Using Tixagevimab-Cilgavimab (Evusheld): Real-World Experience at a Large Academic Center.

机构信息

Division of Infectious Disease, College of Medicine, University of Arizona, Tucson.

Division of Nephrology, Banner University Medical Center, Tucson, Ariz.

出版信息

Am J Med. 2023 Jan;136(1):96-99. doi: 10.1016/j.amjmed.2022.08.019. Epub 2022 Sep 29.

DOI:10.1016/j.amjmed.2022.08.019
PMID:36181789
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9519524/
Abstract

BACKGROUND

Coronavirus disease 2019 (COVID-19) is associated with increased morbidity and mortality among immunocompromised patients. Tixagevimab-cilgavimab (Tix-Cil) is a combination of 2 monoclonal antibodies approved for the prevention of COVID-19 complications in this high-risk group.

METHODS

We retrospectively reviewed the charts of patients who received Tix-Cil during the Omicron variant period (January 17 to April 23, 2022), with a follow-up period until May 24, 2022. We collected data about patient underlying comorbidities and post Tix-Cil COVID-19 infections, deaths, and hospitalizations.

RESULTS

There were 463 patients with a median age of 68 years, of which 51% were male, 79% White, 13.2% Hispanic, 1.7% Black/African American, and 5.8% identified as Other. A total of 18% had undergone a solid organ transplantation or hematopoietic stem cell transplantation. Only 6/98 (6.1%) had severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) detected by polymerase chain reaction (PCR) at a median 48 days (interquartile range [IQR] 27.5, 69) follow-up. Forty-two patients (9.1%) were hospitalized, and 4 (0.9%) died, but none were attributed to COVID-19 or Tix-Cil. One hospitalized patient had an incidental, asymptomatic, positive SARS-CoV 2 by PCR. The median days from Tix-Cil administration to non-COVID-19-related hospitalization and death were 30 (IQR 17, 55) and 53 (IQR 18, 91), respectively.

CONCLUSION

Tix-Cil provides protection against COVID-19 complications in immunocompromised patients with suboptimal immune responses to vaccines.

摘要

背景

2019 年冠状病毒病(COVID-19)与免疫功能低下患者的发病率和死亡率增加有关。Tixagevimab-cilgavimab(Tix-Cil)是一种由 2 种单克隆抗体组成的组合药物,用于预防该高危人群 COVID-19 并发症。

方法

我们回顾性分析了奥密克戎变异期(2022 年 1 月 17 日至 4 月 23 日)期间接受 Tix-Cil 的患者的病历,随访期截至 2022 年 5 月 24 日。我们收集了患者基础合并症以及 Tix-Cil 接种后 COVID-19 感染、死亡和住院的数据。

结果

共有 463 名患者,中位年龄为 68 岁,其中 51%为男性,79%为白人,13.2%为西班牙裔,1.7%为黑种人/非裔美国人,5.8%为其他族裔。总共 18%的患者接受过实体器官移植或造血干细胞移植。只有 6/98(6.1%)例患者在中位随访 48 天(四分位距 [IQR]27.5,69)时通过聚合酶链反应(PCR)检测到严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)。42 名患者(9.1%)住院,4 名患者(0.9%)死亡,但均与 COVID-19 或 Tix-Cil 无关。一名住院患者偶然出现无症状的 SARS-CoV-2 阳性。从 Tix-Cil 给药到非 COVID-19 相关住院和死亡的中位时间分别为 30(IQR17,55)和 53(IQR18,91)天。

结论

Tix-Cil 为疫苗免疫应答欠佳的免疫功能低下患者提供了 COVID-19 并发症的保护。