Evidence map›Paper›PMID 33101309›Full record

ReviewFrontiers in immunology2020

Emerging Concepts and Technologies in Vaccine Development.

Morgan Brisse, Sophia M Vrba, Natalie Kirk, Yuying Liang, Hinh Ly

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 172 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
172citing papers in PubMed, 3 pooled it
4.3field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

172 citing papers in PubMed, 3 syntheses or guidelines pooled it, 317 citations in OpenAlex.

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  18. B-EPIC: A Transformer-Based Language Model for Decoding B Cell Immunodominance Patterns.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  19. A review of vaccinology andHuman vaccines & immunotherapeutics · 2025
    Review
  20. Review

112 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Morgan BrisseBiochemistry, Molecular Biology, and Biophysics Graduate Program, University of Minnesota Twin Cities, St. Paul, MN, United States.
Sophia M VrbaDepartment of Veterinary & Biomedical Sciences, University of Minnesota Twin Cities, St. Paul, MN, United States.
Natalie KirkDepartment of Veterinary & Biomedical Sciences, University of Minnesota Twin Cities, St. Paul, MN, United States.
Yuying LiangDepartment of Veterinary & Biomedical Sciences, University of Minnesota Twin Cities, St. Paul, MN, United States.
Hinh LyDepartment of Veterinary & Biomedical Sciences, University of Minnesota Twin Cities, St. Paul, MN, United States.
University of Minnesota · US

Funding

Training in PharmacoNeuroImmune Substance Abuse ResearchT32DA007097 · NIDA · UNIVERSITY OF MINNESOTA TWIN CITIES · PI MOLITOR, THOMAS WILLIAM · 1985 to 2021
$13.1M
Mechanism of Lassa fever virus Z protein in immune suppression and viral virulenceR01AI131586 · NIAID · UNIVERSITY OF MINNESOTA · PI LIANG, YUYING, LY, HINH · 2017 to 2021
$3.8M
NIDA NIH HHS T32 DA007097
6 · The paper itself

Abstract

Despite the success of vaccination to greatly mitigate or eliminate threat of diseases caused by pathogens, there are still known diseases and emerging pathogens for which the development of successful vaccines against them is inherently difficult. In addition, vaccine development for people with compromised immunity and other pre-existing medical conditions has remained a major challenge. Besides the traditional inactivated or live attenuated, virus-vectored and subunit vaccines, emerging non-viral vaccine technologies, such as viral-like particle and nanoparticle vaccines, DNA/RNA vaccines, and rational vaccine design, offer innovative approaches to address existing challenges of vaccine development. They have also significantly advanced our understanding of vaccine immunology and can guide future vaccine development for many diseases, including rapidly emerging infectious diseases, such as COVID-19, and diseases that have not traditionally been addressed by vaccination, such as cancers and substance abuse. This review provides an integrative discussion of new non-viral vaccine development technologies and their use to address the most fundamental and ongoing challenges of vaccine development.

Indexed as

BetacoronavirusCommunicable Diseases, EmergingCoronavirus InfectionsCOVID-19COVID-19 VaccinesNanoparticlesPandemicsPneumonia, ViralSARS-CoV-2VaccinationVaccines, DNAVaccines, SubunitVaccines, Virus-Like ParticleViral VaccinesCOVID-19 VaccinesVaccines, DNAVaccines, SubunitVaccines, Virus-Like ParticleViral Vaccinescancer vaccinesCOVID19infectious diseasenanoparticle vaccinesnoncommunicable diseasenon-viral DNA-RNA vaccinessubstance abusevirus-like particle vaccines

Identifiers

PMID33101309
PMCPMC7554600
OpenAlexW3089805074

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.