美国奥密克戎、德尔塔和阿尔法SARS-CoV-2变体的临床严重程度和mRNA疫苗有效性:一项前瞻性观察研究。
Clinical Severity and mRNA Vaccine Effectiveness for Omicron, Delta, and Alpha SARS-CoV-2 Variants in the United States: A Prospective Observational Study.
作者信息
Lauring Adam S, Tenforde Mark W, Chappell James D, Gaglani Manjusha, Ginde Adit A, McNeal Tresa, Ghamande Shekhar, Douin David J, Talbot H Keipp, Casey Jonathan D, Mohr Nicholas M, Zepeski Anne, Shapiro Nathan I, Gibbs Kevin W, Files D Clark, Hager David N, Shehu Arber, Prekker Matthew E, Erickson Heidi L, Exline Matthew C, Gong Michelle N, Mohamed Amira, Johnson Nicholas J, Srinivasan Vasisht, Steingrub Jay S, Peltan Ithan D, Brown Samuel M, Martin Emily T, Monto Arnold S, Khan Akram, Hough Catherine L, Busse Laurence W, Ten Lohuis Caitlin C, Duggal Abhijit, Wilson Jennifer G, Gordon Alexandra June, Qadir Nida, Chang Steven Y, Mallow Christopher, Rivas Carolina, Babcock Hilary M, Kwon Jennie H, Halasa Natasha, Grijalva Carlos G, Rice Todd W, Stubblefield William B, Baughman Adrienne, Womack Kelsey N, Rhoads Jillian P, Lindsell Christopher J, Hart Kimberly W, Zhu Yuwei, Adams Katherine, Schrag Stephanie J, Olson Samantha M, Kobayashi Miwako, Verani Jennifer R, Patel Manish M, Self Wesley H
出版信息
medRxiv. 2022 Feb 7:2022.02.06.22270558. doi: 10.1101/2022.02.06.22270558.
OBJECTIVES
To characterize the clinical severity of COVID-19 caused by Omicron, Delta, and Alpha SARS-CoV-2 variants among hospitalized adults and to compare the effectiveness of mRNA COVID-19 vaccines to prevent hospitalizations caused by each variant.
DESIGN
A case-control study of 11,690 hospitalized adults.
SETTING
Twenty-one hospitals across the United States.
PARTICIPANTS
This study included 5728 cases hospitalized with COVID-19 and 5962 controls hospitalized without COVID-19. Cases were classified into SARS-CoV-2 variant groups based on viral whole genome sequencing, and if sequencing did not reveal a lineage, by the predominant circulating variant at the time of hospital admission: Alpha (March 11 to July 3, 2021), Delta (July 4 to December 25, 2021), and Omicron (December 26, 2021 to January 14, 2022).
MAIN OUTCOME MEASURES
Vaccine effectiveness was calculated using a test-negative design for COVID-19 mRNA vaccines to prevent COVID-19 hospitalizations by each variant (Alpha, Delta, Omicron). Among hospitalized patients with COVID-19, disease severity on the WHO Clinical Progression Ordinal Scale was compared among variants using proportional odds regression.
RESULTS
Vaccine effectiveness of the mRNA vaccines to prevent COVID-19-associated hospitalizations included: 85% (95% CI: 82 to 88%) for 2 vaccine doses against Alpha; 85% (95% CI: 83 to 87%) for 2 doses against Delta; 94% (95% CI: 92 to 95%) for 3 doses against Delta; 65% (95% CI: 51 to 75%) for 2 doses against Omicron; and 86% (95% CI: 77 to 91%) for 3 doses against Omicron. Among hospitalized unvaccinated COVID-19 patients, severity on the WHO Clinical Progression Scale was higher for Delta than Alpha (adjusted proportional odds ratio [aPOR] 1.28, 95% CI: 1.11 to 1.46), and lower for Omicron than Delta (aPOR 0.61, 95% CI: 0.49 to 0.77). Compared to unvaccinated cases, severity was lower for vaccinated cases for each variant, including Alpha (aPOR 0.33, 95% CI: 0.23 to 0.49), Delta (aPOR 0.44, 95% CI: 0.37 to 0.51), and Omicron (aPOR 0.61, 95% CI: 0.44 to 0.85).
CONCLUSIONS
mRNA vaccines were highly effective in preventing COVID-19-associated hospitalizations from Alpha, Delta, and Omicron variants, but three vaccine doses were required to achieve protection against Omicron similar to the protection that two doses provided against Delta and Alpha. Among adults hospitalized with COVID-19, Omicron caused less severe disease than Delta, but still resulted in substantial morbidity and mortality. Vaccinated patients hospitalized with COVID-19 had significantly lower disease severity than unvaccinated patients for all the variants.
目的
描述住院成人中由奥密克戎、德尔塔和阿尔法SARS-CoV-2变体引起的新冠病毒病(COVID-19)的临床严重程度,并比较mRNA新冠疫苗预防由每种变体导致的住院的有效性。
设计
一项对11,690名住院成人的病例对照研究。
地点
美国的21家医院。
参与者
本研究纳入了5728例因COVID-19住院的病例和5962例未患COVID-19的住院对照。病例根据病毒全基因组测序被分为SARS-CoV-2变体组,如果测序未揭示谱系,则根据入院时主要流行的变体分类:阿尔法(2021年3月11日至7月3日)、德尔塔(2021年7月4日至12月25日)和奥密克戎(2021年12月26日至2022年1月14日)。
主要结局指标
使用针对COVID-19 mRNA疫苗的检测阴性设计计算预防由每种变体(阿尔法、德尔塔、奥密克戎)导致的COVID-19住院的疫苗有效性。在因COVID-19住院的患者中,使用比例优势回归比较各变体在世卫组织临床进展序贯量表上的疾病严重程度。
结果
mRNA疫苗预防与COVID-19相关住院的有效性包括:2剂疫苗针对阿尔法的有效性为85%(95%置信区间:82%至88%);2剂针对德尔塔的有效性为85%(95%置信区间:83%至87%);3剂针对德尔塔的有效性为94%(95%置信区间:92%至95%);2剂针对奥密克戎的有效性为65%(95%置信区间:51%至75%);3剂针对奥密克戎的有效性为86%(95%置信区间:77%至91%)。在未接种疫苗的COVID-19住院患者中,德尔塔在世卫组织临床进展量表上的严重程度高于阿尔法(调整后的比例优势比[aPOR]为1.28,95%置信区间:1.11至1.46),奥密克戎的严重程度低于德尔塔(aPOR为0.61,95%置信区间:0.49至0.77)。与未接种疫苗的病例相比,每种变体的接种疫苗病例的严重程度均较低,包括阿尔法(aPOR为0.33,95%置信区间:0.23至0.49)、德尔塔(aPOR为0.44,95%置信区间:0.37至0.51)和奥密克戎(aPOR为0.61,95%置信区间:0.44至0.85)。
结论
mRNA疫苗在预防由阿尔法、德尔塔和奥密克戎变体导致的与COVID-19相关住院方面非常有效,但需要3剂疫苗才能获得与2剂疫苗针对德尔塔和阿尔法所提供的保护相似的针对奥密克戎的保护。在因COVID-19住院的成人中,奥密克戎导致的疾病严重程度低于德尔塔,但仍导致大量发病和死亡。对于所有变体,因COVID-19住院的接种疫苗患者的疾病严重程度明显低于未接种疫苗的患者。