Evidence map›Paper›PMID 35332581›Full record

ArticleAdvanced materials (Deerfield Beach, Fla.)2022

Rational Development of a Polysaccharide-Protein-Conjugated Nanoparticle Vaccine Against SARS-CoV-2 Variants and Streptococcus pneumoniae.

Yongqiang Deng, Jing Li, Chunyun Sun, Hang Chi, Dan Luo, Rui Wang, Hongying Qiu, Yanjing Zhang, Mei Wu, Xiao Zhang and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Advanced materials (Deerfield Beach, Fla.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Nanocarrier-based immunotherapy for viral diseases.International journal of pharmaceutics: X · 2025
    Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Insights for COVID-19 in 2023.Revista espanola de quimioterapia : publicacion oficial de la Sociedad Espanola de Quimioterapia · 2023
    Review
  10. Article
  11. Review
  12. Review
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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

13 authors at 3 institutions in 2 countries.

Yongqiang DengDepartment of Virology, State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, AMMS, Beijing, 100071, P. R. China.
Jing LiBeijing Protein and Antibody R&D Engineering Center, Sinocelltech Ltd., Beijing, 100176, P. R. China.
Chunyun SunBeijing Protein and Antibody R&D Engineering Center, Sinocelltech Ltd., Beijing, 100176, P. R. China.
Hang ChiDepartment of Virology, State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, AMMS, Beijing, 100071, P. R. China.
Dan LuoDepartment of Virology, State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, AMMS, Beijing, 100071, P. R. China.
Rui WangBeijing Protein and Antibody R&D Engineering Center, Sinocelltech Ltd., Beijing, 100176, P. R. China.
Hongying QiuDepartment of Virology, State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, AMMS, Beijing, 100071, P. R. China.
Yanjing ZhangBeijing Protein and Antibody R&D Engineering Center, Sinocelltech Ltd., Beijing, 100176, P. R. China.
Mei WuDepartment of Virology, State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, AMMS, Beijing, 100071, P. R. China.
Xiao ZhangBeijing Protein and Antibody R&D Engineering Center, Sinocelltech Ltd., Beijing, 100176, P. R. China.
Xun HuangDepartment of Virology, State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, AMMS, Beijing, 100071, P. R. China.
Liangzhi XieBeijing Protein and Antibody R&D Engineering Center, Sinocelltech Ltd., Beijing, 100176, P. R. China.
Chengfeng QinDepartment of Virology, State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, AMMS, Beijing, 100071, P. R. China.ORCID https://orcid.org/0000-0002-0632-2807
Institute of Microbiology · BYSinocelltech Group (China) · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

Beijing Municipal Science and Technology Program Z211100002521026Innovation Fund for Medical Sciences from the Chinese Academy of Medical Sciences 2019-I2M-5-049Innovative Research Group from NSFC 81621005National Natural Science Foundation of China 32130005National Natural Science Foundation of China 82174055National Science Fund for Distinguished Young Scholars 81925025
6 · The paper itself

Abstract

The ongoing COVID-19 pandemic caused by SARS-CoV-2 has led to millions of deaths worldwide. Streptococcus pneumoniae (S. pneumoniae) remains a major cause of mortality in underdeveloped countries. A vaccine that prevents both SARS-CoV-2 and S. pneumoniae infection represents a long-sought "magic bullet". Herein, a nanoparticle vaccine, termed SCTV01B, is rationally developed by using the capsular polysaccharide of S. pneumoniae serotype 14 (PPS14) as the backbone to conjugate with the recombinant receptor-binding domain (RBD) of the SARS-CoV-2 spike protein. The final formulation of conjugated nanoparticles in the network structure exhibits high thermal stability. Immunization with SCTV01B induces potent humoral and Type 1/Type 2 T helper cell (Th1/Th2) cellular immune responses in mice, rats, and rhesus macaques. In particular, SCTV01B-immunized serum not only broadly cross-neutralizes all SARS-CoV-2 variants of concern (VOCs), including the most recent Omicron variant, but also shows high opsonophagocytic activity (OPA) against S. pneumoniae serotype 14. Finally, SCTV01B vaccination confers protection against challenges with the SARS-CoV-2 mouse-adapted strain and the original strain in established murine models. Collectively, these promising preclinical results support further clinical evaluation of SCTV01B, highlighting the potency of polysaccharide-RBD-conjugated nanoparticle vaccine platforms for the development of vaccines for COVID-19 and other infectious diseases.

Indexed as

COVID-19NanoparticlesVaccinesAnimalsAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesHumansMacaca mulattaMicePandemicsPolysaccharidesRatsSARS-CoV-2Spike Glycoprotein, CoronavirusStreptococcus pneumoniaeAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesPolysaccharidesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Vaccinescapsular polysaccharidechemical conjugationnanoparticle vaccinesreceptor binding domainSARS-CoV-2S. pneumoniae serotype type 14

Identifiers

PMID35332581
PMCPMC9073961
OpenAlexW4221073962

What OpenQuestion holds

Textmetadata
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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.