Evidence map›Paper›PMID 34694917›Full record

ArticleInfection and immunity2022

Novel Pneumococcal Protein-Polysaccharide Conjugate Vaccine Based on Biotin-Streptavidin.

Mengze Guo, Xiaonan Guo, Chenxing Zhang, Shidong Zhu, Yue Zhang, Tiejun Gu, Wei Kong, Yongge Wu

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
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

8 authors at 1 institution in 1 country.

Mengze GuoNational Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin Universitygrid.64924.3d, Changchun, People's Republic of China.
Xiaonan GuoNational Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin Universitygrid.64924.3d, Changchun, People's Republic of China.
Chenxing ZhangNational Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin Universitygrid.64924.3d, Changchun, People's Republic of China.
Shidong ZhuNational Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin Universitygrid.64924.3d, Changchun, People's Republic of China.
Yue ZhangQingDaogaoxin Vocational School, Qingdao, People's Republic of China.
Tiejun GuNational Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin Universitygrid.64924.3d, Changchun, People's Republic of China.
Wei KongNational Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin Universitygrid.64924.3d, Changchun, People's Republic of China.
Yongge WuNational Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin Universitygrid.64924.3d, Changchun, People's Republic of China.
Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pneumococcal disease is a serious public health problem worldwide and an important cause of morbidity and mortality among children and adults in developing countries. Although vaccination is among the most effective approaches to prevent and control pneumococcal diseases, approved vaccines have limited protective effects. We developed a pneumococcal protein-polysaccharide conjugate vaccine that is mediated by the noncovalent interaction between biotin and streptavidin. Biotinylated type IV capsular polysaccharide was incubated with a fusion protein containing core streptavidin and Streptococcus pneumoniae virulence protein and relied on the noncovalent interaction between biotin and streptavidin to prepare the protein-polysaccharide conjugate vaccine. Analysis of vaccine efficacy revealed that mice immunized with the protein-polysaccharide conjugate vaccine produced antibodies with high potency against virulence proteins and polysaccharide antigens and were able to induce Th1 and Th17 responses. The antibodies identified using an opsonophagocytic assay were capable of activating the complement system and promoting pathogen elimination by phagocytes. Additionally, mice immunized with the protein-polysaccharide conjugate vaccine and then infected with a lethal dose of Streptococcus pneumoniae demonstrated induced protective immunity. The data indicated that the pneumococcal protein-polysaccharide (biotin-streptavidin) conjugate vaccine demonstrated broad-spectrum activity applicable to a wide range of people and ease of direct coupling between protein and polysaccharide. These findings provide further evidence for the application of biotin-streptavidin in S. pneumoniae vaccines.

Indexed as

BiotinStreptavidinAntibodies, BacterialAntigens, BacterialChromatography, High Pressure LiquidHumansImmunity, CellularImmunity, HumoralImmunizationImmunogenicity, VaccinePneumococcal InfectionsPneumococcal VaccinesSpectrum AnalysisStreptococcus pneumoniaeVaccine DevelopmentVaccines, ConjugateAntibodies, BacterialAntigens, BacterialBiotinPneumococcal VaccinesStreptavidinVaccines, Conjugatebiotinpneumococcal surface adhesin Apneumococcal surface protein Aprotein-polysaccharide conjugate vaccinestreptavidinStreptococcus pneumoniae

Identifiers

PMID34694917
PMCPMC8788663
OpenAlexW3208993800

What OpenQuestion holds

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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.