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mRNA加强疫苗对有和无免疫功能障碍的人预防2019冠状病毒病感染及严重后果的有效性:一项基于美国国家电子病历数据的回顾性队列研究

Effectiveness of mRNA Booster Vaccine Against Coronavirus Disease 2019 Infection and Severe Outcomes Among Persons With and Without Immune Dysfunction: A Retrospective Cohort Study of National Electronic Medical Record Data in the United States.

作者信息

Sun Jing, Zheng Qulu, Anzalone Alfred J, Abraham Alison G, Olex Amy L, Zhang Yifan, Mathew Jomol, Safdar Nasia, Haendel Melissa A, Segev Dorry, Islam Jessica Y, Singh Jasvinder A, Mannon Roslyn B, Chute Christopher G, Patel Rena C, Kirk Gregory D

机构信息

Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.

Department of Neurological Sciences, University of Nebraska Medical Center, Omaha, Nebraska, USA.

出版信息

Open Forum Infect Dis. 2024 Jan 11;11(2):ofae019. doi: 10.1093/ofid/ofae019. eCollection 2024 Feb.

Abstract

BACKGROUND

Real-world evidence of coronavirus disease 2019 (COVID-19) messenger RNA (mRNA) booster effectiveness among patients with immune dysfunction are limited.

METHODS

We included data from patients in the United States National COVID Cohort Collaborative (N3C) who completed ≥2 doses of mRNA vaccination between 10 December 2020 and 27 May 2022. Immune dysfunction conditions included human immunodeficiency virus infection, solid organ or bone marrow transplant, autoimmune diseases, and cancer. We defined incident COVID-19 BTI as positive results from laboratory tests or diagnostic codes 14 days after at least 2 doses of mRNA vaccination; and severe COVID-19 BTI as hospitalization, invasive cardiopulmonary support, and/or death. We used propensity scores to match boosted versus nonboosted patients and evaluated hazards of incident and severe COVID-19 BTI using Cox regression after matching.

RESULTS

Among patients without immune dysfunction, the relative effectiveness of booster (3 doses) after 6 months from the primary (2 doses) vaccination against BTI ranged from 69% to 81% during the Delta-predominant period and from 33% to 39% during the Omicron-predominant period. Relative effectiveness against BTI was lower among patients with immune dysfunction but remained statistically significant in both periods. Boosted patients had lower risk of COVID-19-related hospitalization (hazard ratios [HR] ranged from 0.5 [95% confidence interval {CI}, .48-.53] to 0.63 [95% CI, .56-.70]), invasive cardiopulmonary support, or death (HRs ranged from 0.46 [95% CI, .41-.52] to 0.63 [95% CI, .50-.79]) during both periods.

CONCLUSIONS

Booster vaccines remain effective against severe COVID-19 BTI throughout the Delta- and Omicron-predominant periods, regardless of patients' immune status.

摘要

背景

2019冠状病毒病(COVID-19)信使核糖核酸(mRNA)加强针在免疫功能低下患者中的真实世界证据有限。

方法

我们纳入了美国国家COVID队列协作组(N3C)中在2020年12月10日至2022年5月27日期间完成≥2剂mRNA疫苗接种的患者数据。免疫功能障碍情况包括人类免疫缺陷病毒感染、实体器官或骨髓移植、自身免疫性疾病和癌症。我们将确诊的COVID-19突破性感染定义为至少2剂mRNA疫苗接种14天后实验室检测或诊断编码呈阳性结果;将重症COVID-19突破性感染定义为住院、侵入性心肺支持和/或死亡。我们使用倾向评分来匹配接种加强针与未接种加强针的患者,并在匹配后使用Cox回归评估确诊和重症COVID-19突破性感染的风险。

结果

在无免疫功能障碍的患者中,初次(2剂)接种疫苗6个月后加强针(3剂)对突破性感染的相对有效性在以德尔塔毒株为主的时期为69%至81%,在以奥密克戎毒株为主的时期为33%至39%。免疫功能障碍患者中加强针预防突破性感染的相对有效性较低,但在两个时期均保持统计学显著性。接种加强针的患者在两个时期发生COVID-19相关住院(风险比[HR]范围为0.5[95%置信区间{CI},0.48 - 0.53]至0.63[95%CI,0.56 - 0.70])、侵入性心肺支持或死亡(HR范围为0.46[95%CI,0.41 - 0.52]至0.63[95%CI,0.50 - 0.79])的风险较低。

结论

在以德尔塔毒株和奥密克戎毒株为主的整个时期,加强针疫苗对重症COVID-19突破性感染仍然有效,无论患者的免疫状态如何。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3524/10878052/63eb640c362b/ofae019f1.jpg

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