Evidence map›Paper›PMID 36474858›Full record

ArticleMedComm2022

Mixed formulation of mRNA and protein-based COVID-19 vaccines triggered superior neutralizing antibody responses.

Jialu Zhang, Qian He, Xujia Yan, Jianyang Liu, Yu Bai, Chaoqiang An, Bopei Cui, Fan Gao, Qunying Mao, Junzhi Wang and 2 more

Open access · goldAbstract read
In one paragraph

Article in MedComm, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

8 citing papers in PubMed, 5 citations in OpenAlex.

  1. Development of mRNA vaccines against herpes zoster.Human vaccines & immunotherapeutics · 2026
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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

12 authors at 2 institutions in 1 country.

Jialu ZhangDivision of Hepatitis and Enterovirus Vaccines, Institute of Biological Products, National Institutes for Food and Drug Control NHC Key Laboratory of Research on Quality and Standardization of Biotech Products, NMPA Key Laboratory for Quality Research and Evaluation of Biological Products Beijing People's Republic of China.
Qian HeDivision of Hepatitis and Enterovirus Vaccines, Institute of Biological Products, National Institutes for Food and Drug Control NHC Key Laboratory of Research on Quality and Standardization of Biotech Products, NMPA Key Laboratory for Quality Research and Evaluation of Biological Products Beijing People's Republic of China.
Xujia YanDivision of Hepatitis and Enterovirus Vaccines, Institute of Biological Products, National Institutes for Food and Drug Control NHC Key Laboratory of Research on Quality and Standardization of Biotech Products, NMPA Key Laboratory for Quality Research and Evaluation of Biological Products Beijing People's Republic of China.
Jianyang LiuDivision of Hepatitis and Enterovirus Vaccines, Institute of Biological Products, National Institutes for Food and Drug Control NHC Key Laboratory of Research on Quality and Standardization of Biotech Products, NMPA Key Laboratory for Quality Research and Evaluation of Biological Products Beijing People's Republic of China.
Yu BaiDivision of Hepatitis and Enterovirus Vaccines, Institute of Biological Products, National Institutes for Food and Drug Control NHC Key Laboratory of Research on Quality and Standardization of Biotech Products, NMPA Key Laboratory for Quality Research and Evaluation of Biological Products Beijing People's Republic of China.
Chaoqiang AnDivision of Hepatitis and Enterovirus Vaccines, Institute of Biological Products, National Institutes for Food and Drug Control NHC Key Laboratory of Research on Quality and Standardization of Biotech Products, NMPA Key Laboratory for Quality Research and Evaluation of Biological Products Beijing People's Republic of China.
Bopei CuiDivision of Hepatitis and Enterovirus Vaccines, Institute of Biological Products, National Institutes for Food and Drug Control NHC Key Laboratory of Research on Quality and Standardization of Biotech Products, NMPA Key Laboratory for Quality Research and Evaluation of Biological Products Beijing People's Republic of China.
Fan GaoDivision of Hepatitis and Enterovirus Vaccines, Institute of Biological Products, National Institutes for Food and Drug Control NHC Key Laboratory of Research on Quality and Standardization of Biotech Products, NMPA Key Laboratory for Quality Research and Evaluation of Biological Products Beijing People's Republic of China.
Qunying MaoDivision of Hepatitis and Enterovirus Vaccines, Institute of Biological Products, National Institutes for Food and Drug Control NHC Key Laboratory of Research on Quality and Standardization of Biotech Products, NMPA Key Laboratory for Quality Research and Evaluation of Biological Products Beijing People's Republic of China.
Junzhi WangDivision of Hepatitis and Enterovirus Vaccines, Institute of Biological Products, National Institutes for Food and Drug Control NHC Key Laboratory of Research on Quality and Standardization of Biotech Products, NMPA Key Laboratory for Quality Research and Evaluation of Biological Products Beijing People's Republic of China.
Miao XuDivision of Hepatitis and Enterovirus Vaccines, Institute of Biological Products, National Institutes for Food and Drug Control NHC Key Laboratory of Research on Quality and Standardization of Biotech Products, NMPA Key Laboratory for Quality Research and Evaluation of Biological Products Beijing People's Republic of China.
Zhenglun LiangDivision of Hepatitis and Enterovirus Vaccines, Institute of Biological Products, National Institutes for Food and Drug Control NHC Key Laboratory of Research on Quality and Standardization of Biotech Products, NMPA Key Laboratory for Quality Research and Evaluation of Biological Products Beijing People's Republic of China.
National Medical Products Administration · CNNational Institutes for Food and Drug Control · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Integrating different types of vaccines into a singular immunization regimen is an effective and accessible approach to strengthen and broaden the immunogenicity of existing coronavirus disease 2019 (COVID-19) vaccine candidates. To optimize the immunization strategy of the novel mRNA-based vaccine and recombinant protein subunit vaccine that attracted much attention in COVID-19 vaccine development, we evaluated the immunogenicity of different combined regimens with the mRNA vaccine (RNA-RBD) and protein subunit vaccine (PS-RBD) in mice. Compared with homologous immunization of RNA-RBD or PS-RBD, heterologous prime-boost strategies for mRNA and protein subunit vaccines failed to simultaneously enhance neutralizing antibody (NAb) and Th1 cellular response in this study, showing modestly higher serum neutralizing activity and antibody-dependent cell-mediated cytotoxicity for "PS-RBD prime, RNA-RBD boost" and robust Th1 type cellular response for "RNA-RBD prime, PS-RBD boost". Interestingly, immunizing the mice with the mixed formulation of the two aforementioned vaccines in various proportions further significantly enhanced the NAb responses against ancestral, Delta, and Omicron strains and manifested increased Th1-type responses, suggesting that a mixed formulation of mRNA and protein vaccines might be a more prospective vaccination strategy. This study provides basic research data on the combined vaccination strategies of mRNA and protein-based COVID-19 vaccines.

Indexed as

COVID‐19 vaccineheterologous prime‐boostneutralizing antibodySARS‐CoV‐2Th1 response

Identifiers

PMID36474858
PMCPMC9717706
OpenAlexW4310954710

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.