Comparative Effectiveness of Coronavirus Disease 2019 (COVID-19) Vaccines Against the Delta Variant

被引:22
作者
Risk, Malcolm [1 ]
Shen, Chen [1 ]
Hayek, Salim S. [2 ]
Holevinski, Lynn [3 ]
Schiopu, Elena [4 ]
Freed, Gary [5 ,6 ]
Akin, Cem [7 ]
Zhao, Lili [1 ]
机构
[1] Univ Michigan, Dept Biostat, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Med, Div Cardiol, Ann Arbor, MI 48109 USA
[3] Off Res, Data Off Clin & Translat Res, Ann Arbor, MI USA
[4] Internal Med, Rheumatol, Ann Arbor, MI USA
[5] Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA
[6] Univ Michigan, Dept Hlth Management & Policy, Ann Arbor, MI 48109 USA
[7] Univ Michigan, Div Allergy, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
COVID-19; vaccines; waning immunity; comparative effectiveness; Delta variant;
D O I
10.1093/cid/ciac106
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background There is a lack of data regarding how the Delta variant of coronavirus disease 2019 (COVID-19) has impacted the effectiveness of the BNT162b2 (Pfizer-BioNTech), mRNA-1273 (Moderna), and Ad26.COV2.S (Johnson & Johnson-Janssen) vaccines at preventing severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and COVID-19 hospitalization. Methods We compared the effectiveness of the three vaccines during the pre- and post-Delta variant period (before and after 1 July 2021) in a large cohort of vaccinated and unvaccinated patients in the Michigan Medicine healthcare system. We assessed vaccine effectiveness (VE) using 2 analyses: an inverse propensity weighted (IPW) Kaplan-Meier (KM) analysis based on time from vaccination, and a Cox model based on calendar time with vaccination as a time-varying covariate. Results Compared to Ad26.COV2.S recipients, the risk of hospitalization for COVID-19 in the post-Delta variant period was lower for BNT162b2 recipients (hazard ratio [HR] = 0.37; 95% confidence interval [CI]: [.14-.98]; P = .05) and mRNA-1273 recipients (HR = 0.21; 95% CI: [.07-.64]; P = .006). Recipients of the mRNA-1273 vaccine had a lower risk of SARS-CoV-2 infection than Ad26.COV2.S recipients (HR = 0.6; 95% CI: [.43-.83]; P = .003) and BNT162b2 recipients (HR = 0.64; 95% CI: [.54-.76]; P < .001). After 1 July, efficacy against SARS-CoV-2 infection declined for Ad26.COV2.S recipients (VE = 76% before; VE = 49% after; P = .02), BNT162b2 recipients (VE = 87% before; VE = 52% after; P < .001), and mRNA-1273 recipients (VE = 92% before; VE = 70% after; P < .001). Waning immunity and the Delta variant contributed independently and significantly to this decline. Conclusions Although there is a substantial decline in effectiveness, the approved COVID-19 vaccines remain effective against infection and hospitalization due to the Delta variant. The mRNA-based vaccines are more effective than the Ad26.COV2.S vaccine. The COVID-19 vaccines have reduced effectiveness against the Delta variant for SARS-CoV-2 infection and COVID-19 hospitalization. The effectiveness of mRNA-based vaccines against Delta hospitalization is substantially greater than the effectiveness of the Ad26.COV2.S (Johnson & Johnson-Janssen) vaccine.
引用
收藏
页码:E623 / E629
页数:7
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