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Comparative Effectiveness of Moderna, Pfizer-BioNTech, and Janssen (Johnson & Johnson) Vaccines in Preventing COVID-19 Hospitalizations Among Adults Without Immunocompromising Conditions - United States, March-August 2021.

作者信息

Self Wesley H, Tenforde Mark W, Rhoads Jillian P, Gaglani Manjusha, Ginde Adit A, Douin David J, Olson Samantha M, Talbot H Keipp, Casey Jonathan D, Mohr Nicholas M, Zepeski Anne, McNeal Tresa, Ghamande Shekhar, Gibbs Kevin W, Files D Clark, Hager David N, Shehu Arber, Prekker Matthew E, Erickson Heidi L, Gong Michelle N, Mohamed Amira, Henning Daniel J, 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, Exline Matthew C, Halasa Natasha, Chappell James D, Lauring Adam S, Grijalva Carlos G, Rice Todd W, Jones Ian D, Stubblefield William B, Baughman Adrienne, Womack Kelsey N, Lindsell Christopher J, Hart Kimberly W, Zhu Yuwei, Mills Lisa, Lester Sandra N, Stumpf Megan M, Naioti Eric A, Kobayashi Miwako, Verani Jennifer R, Thornburg Natalie J, Patel Manish M

出版信息

MMWR Morb Mortal Wkly Rep. 2021 Sep 24;70(38):1337-1343. doi: 10.15585/mmwr.mm7038e1.


DOI:10.15585/mmwr.mm7038e1
PMID:34555004
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8459899/
Abstract

Three COVID-19 vaccines are authorized or approved for use among adults in the United States (1,2). Two 2-dose mRNA vaccines, mRNA-1273 from Moderna and BNT162b2 from Pfizer-BioNTech, received Emergency Use Authorization (EUA) by the Food and Drug Administration (FDA) in December 2020 for persons aged ≥18 years and aged ≥16 years, respectively. A 1-dose viral vector vaccine (Ad26.COV2 from Janssen [Johnson & Johnson]) received EUA in February 2021 for persons aged ≥18 years (3). The Pfizer-BioNTech vaccine received FDA approval for persons aged ≥16 years on August 23, 2021 (4). Current guidelines from FDA and CDC recommend vaccination of eligible persons with one of these three products, without preference for any specific vaccine (4,5). To assess vaccine effectiveness (VE) of these three products in preventing COVID-19 hospitalization, CDC and collaborators conducted a case-control analysis among 3,689 adults aged ≥18 years who were hospitalized at 21 U.S. hospitals across 18 states during March 11-August 15, 2021. An additional analysis compared serum antibody levels (anti-spike immunoglobulin G [IgG] and anti-receptor binding domain [RBD] IgG) to SARS-CoV-2, the virus that causes COVID-19, among 100 healthy volunteers enrolled at three hospitals 2-6 weeks after full vaccination with the Moderna, Pfizer-BioNTech, or Janssen COVID-19 vaccine. Patients with immunocompromising conditions were excluded. VE against COVID-19 hospitalizations was higher for the Moderna vaccine (93%; 95% confidence interval [CI] = 91%-95%) than for the Pfizer-BioNTech vaccine (88%; 95% CI = 85%-91%) (p = 0.011); VE for both mRNA vaccines was higher than that for the Janssen vaccine (71%; 95% CI = 56%-81%) (all p<0.001). Protection for the Pfizer-BioNTech vaccine declined 4 months after vaccination. Postvaccination anti-spike IgG and anti-RBD IgG levels were significantly lower in persons vaccinated with the Janssen vaccine than the Moderna or Pfizer-BioNTech vaccines. Although these real-world data suggest some variation in levels of protection by vaccine, all FDA-approved or authorized COVID-19 vaccines provide substantial protection against COVID-19 hospitalization.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79ab/8459899/ebffcce5e399/mm7038e1-F.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79ab/8459899/ebffcce5e399/mm7038e1-F.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79ab/8459899/ebffcce5e399/mm7038e1-F.jpg

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[1]
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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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[2]
Over- and under-estimation of vaccine effectiveness.

BMC Med Res Methodol. 2025-7-1

[3]
Association of vaccination status and immunosuppression with mortality of SARS-CoV-2 infection in patients with fibrotic interstitial lung disease.

BMJ Open Respir Res. 2025-6-24

[4]
Artificial intelligence-driven circRNA vaccine development: multimodal collaborative optimization and a new paradigm for biomedical applications.

Brief Bioinform. 2025-5-1

[5]
Intensity of public health and social measures are associated with effectiveness of SARS-CoV-2 vaccine in test-negative study.

medRxiv. 2025-5-8

[6]
A Big Data Optimization Approach for Estimating the Time-Dependent Effectiveness Profiles Against Hospitalization for Double- and Single-Dose Schemes: Study Case, COVID-19 in Elderly Mexicans.

Vaccines (Basel). 2025-3-28

[7]
Applications of mRNA Delivery in Cancer Immunotherapy.

Int J Nanomedicine. 2025-3-17

[8]
Joint analysis of time-varying effect of vaccine and antiviral drug for preventing severe complications and mortality.

Sci Rep. 2025-2-15

[9]
Impact of SARS-CoV-2 vaccination and of seasonal variations on the innate immune inflammatory response.

Front Immunol. 2025-1-14

[10]
COVID-19 Vaccines Effectiveness and Safety in Trinidad and Tobago: A Systematic Review and Meta-Analysis.

Microorganisms. 2025-1-10

本文引用的文献

[1]
Sustained Effectiveness of Pfizer-BioNTech and Moderna Vaccines Against COVID-19 Associated Hospitalizations Among Adults - United States, March-July 2021.

MMWR Morb Mortal Wkly Rep. 2021-8-27

[2]
Effectiveness of Pfizer-BioNTech and Moderna Vaccines in Preventing SARS-CoV-2 Infection Among Nursing Home Residents Before and During Widespread Circulation of the SARS-CoV-2 B.1.617.2 (Delta) Variant - National Healthcare Safety Network, March 1-August 1, 2021.

MMWR Morb Mortal Wkly Rep. 2021-8-27

[3]
Effectiveness of Severe Acute Respiratory Syndrome Coronavirus 2 Messenger RNA Vaccines for Preventing Coronavirus Disease 2019 Hospitalizations in the United States.

Clin Infect Dis. 2022-5-3

[4]
Neutralizing antibody levels are highly predictive of immune protection from symptomatic SARS-CoV-2 infection.

Nat Med. 2021-7

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