Cited by 271vaccines and immunoinformatics approachesSARS-CoV-2 and COVID-19 ResearchImmunotherapy and Immune Responses

Designing Tomorrow's Vaccines

Open access
Nabel, Gary J.·2013·New England Journal of Medicine

Abstract

an nejm app for iphoneThe NEJM Image Challenge app brings a popular online feature to the smartphone.Optimized for viewing on the iPhone and iPod Touch, the Image Challenge app lets you test your diagnostic skills anytime, anywhere.The Image Challenge app randomly selects from 300 challenging clinical photos published in NEJM, with a new image added each week.View an image, choose your answer, get immediate feedback, and see how others answered.The Image Challenge app is available at the iTunes App Store.

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  • Vaccines based on mRNA offer multifaceted advantages including flexible antigen design, a cost-effective manufacturing process allowing for parallel production of multiple mRNA vaccines, and rapid manufacturing.

    “Vaccines based on mRNA could meet these requirements because they offer multifaceted advantages including flexible antigen design, a cost-effective manufacturing process allowing for parallel production of multiple mRNA vaccines1–5 and rapid manufacturing, which could be of crucial importance during pandemics.6”

    From Unmodified mRNA in LNPs constitutes a competitive technology for prophylactic vaccines (2017) · cites this paper as [5]

    The opening section says older vaccine technologies were ill-suited to a rapid response to the 2009 H1N1 pandemic, but it does not say mRNA vaccines can be manufactured rapidly. The passages on manufacturing and gene-based delivery likewise do not address mRNA vaccine production, its cost, or parallel production (searched: mRNA vaccines, messenger RNA, rapid manufacturing). (LLM, conf=0.76)

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References 50 · Cited by 271

Authors
Nabel, G. J.
Affiliations
National Institutes of Health (US)
Corresponding author
Nabel, Gary J.
Venue
New England Journal of Medicine
Published
2013-02-07
Volume
368
Issue
6
Pages
551-560
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W2027210355
Cited by
271
References
50
Citations by year
2026: 5 · 2025: 6 · 2024: 11 · 2023: 17 · 2022: 11 · 2021: 22 · 2020: 33 · 2019: 15 · 2018: 23 · 2017: 19 · 2016: 21 · 2015: 37 · 2014: 30 · 2013: 20 · 2012: 1
FWCI
3.42
Type
journal article
Language
en
Open access
Locations
  • New England Journal of Medicine (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • Sanofi
  • National Institutes of Health (Z99 AI999999)
  • National Institute of Allergy and Infectious Diseases (Y99 AI999999, ZIAAI005002, Z01AI005003, Z01AI005002, ZIAAI005058, ZIAAI005003)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › vaccines and immunoinformatics approaches
  • Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
  • Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
Keywords
vaccine design, vaccines
MeSH terms
Allergy and Immunology, Clinical Trials as Topic, Communicable Disease Control, Communicable Diseases, Dendritic Cells, Humans, Licensure, Vaccines, Drug Design, Evolution, Molecular, History, 19th Century, History, 20th Century, History, 21st Century, Host-Pathogen Interactions, Antibodies, Neutralizing, Translational Research, Biomedical

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