Evidence map›Paper›PMID 37271785›Full record

ArticleNPJ vaccines2023

Analyzing immune responses to varied mRNA and protein vaccine sequences.

Hyeong-Jun Park, Yoo-Jin Bang, Sung Pil Kwon, Woori Kwak, Sang-In Park, Gahyun Roh, Seo-Hyeon Bae, Jae-Yong Kim, Hye Won Kwak, Yongkwan Kim and 6 more

Open access · goldAbstract read
In one paragraph

Article in NPJ vaccines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
8.5field-weighted citation impact, top 1% 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

37 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
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  6. Designing 5' UTR sequences improves the capacity of mRNA therapeutics in preclinical models of aging and obesity.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
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  14. 3AIM-seq: Quality assessment of mRNA therapeutics using sequencing for 3' poly(A) tails of in vitro-transcribed mRNA.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
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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

16 authors at 4 institutions in 1 country.

Hyeong-Jun Park *Department of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, Republic of Korea.
Yoo-Jin Bang *Department of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, Republic of Korea.
Sung Pil Kwon *Center for Brain Technology, Brain Science Institute, Korea Institute of Science and Technology, Seoul, 02792, Republic of Korea.
Woori Kwak *Department of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, Republic of Korea.
Sang-In Park *SML Biopharm, Gwangmyeong, 14353, Republic of Korea.
Gahyun RohDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, Republic of Korea.
Seo-Hyeon BaeDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, Republic of Korea.
Jae-Yong KimDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, Republic of Korea.
Hye Won KwakSML Biopharm, Gwangmyeong, 14353, Republic of Korea.
Yongkwan KimSML Biopharm, Gwangmyeong, 14353, Republic of Korea.
Soyeon YooCenter for Brain Technology, Brain Science Institute, Korea Institute of Science and Technology, Seoul, 02792, Republic of Korea.ORCID http://orcid.org/0000-0002-5734-2517
Daegeun KimSML Biopharm, Gwangmyeong, 14353, Republic of Korea.
Gyochang KeumCenter for Brain Technology, Brain Science Institute, Korea Institute of Science and Technology, Seoul, 02792, Republic of Korea.ORCID http://orcid.org/0000-0001-8767-8022
Eun-Kyoung BangCenter for Brain Technology, Brain Science Institute, Korea Institute of Science and Technology, Seoul, 02792, Republic of Korea. eunkbang@kist.re.kr.
So-Hee HongDepartment of Microbiology, College of Medicine, Ewha Womans University, Seoul, 07804, Republic of Korea. hongsohee@gmail.com.
Jae-Hwan NamDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, Republic of Korea. jhnam@catholic.ac.kr.ORCID http://orcid.org/0000-0002-0974-4343
Hanall Biopharma (South Korea) · KRCatholic University of Korea · KRKorea Institute of Brain Science · KREwha Womans University · KR

Funding

Ministry of Food and Drug Safety (MFDS) 22213MFDS421National Research Foundation of Korea (NRF) NRF-2021M3E5E3080558National Research Foundation of Korea (NRF) NRF-2021M3E5E3080563
6 · The paper itself

Abstract

In response to the COVID-19 pandemic, different types of vaccines, such as inactive, live-attenuated, messenger RNA (mRNA), and protein subunit, have been developed against SARS-CoV-2. This has unintentionally created a unique scenario where heterologous prime-boost vaccination against a single virus has been administered to a large human population. Here, we aimed to analyze whether the immunization order of vaccine types influences the efficacy of heterologous prime-boost vaccination, especially mRNA and protein-based vaccines. We developed a new mRNA vaccine encoding the hemagglutinin (HA) glycoprotein of the influenza virus using the 3'-UTR and 5'-UTR of muscle cells (mRNA-HA) and tested its efficacy by heterologous immunization with an HA protein vaccine (protein-HA). The results demonstrated higher IgG2a levels and hemagglutination inhibition titers in the mRNA-HA priming/protein-HA boosting (R-P) regimen than those induced by reverse immunization (protein-HA priming/mRNA-HA boosting, P-R). After the viral challenge, the R-P group showed lower virus loads and less inflammation in the lungs than the P-R group did. Transcriptome analysis revealed that the heterologous prime-boost groups had differentially activated immune response pathways, according to the order of immunization. In summary, our results demonstrate that the sequence of vaccination is critical to direct desired immune responses. This study demonstrates the potential of a heterologous vaccination strategy using mRNA and protein vaccine platforms against viral infection.

Identifiers

PMID37271785
PMCPMC10239716
OpenAlexW4379376969

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.