Evidence map›Paper›PMID 25483702›Full record

ArticleHuman vaccines & immunotherapeutics2014

Development of a heat-stable and orally delivered recombinant M2e-expressing B. subtilis spore-based influenza vaccine.

Guangyu Zhao, Yu Miao, Yan Guo, Hongjie Qiu, Shihui Sun, Zhihua Kou, Hong Yu, Junfeng Li, Yue Chen, Shibo Jiang and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

17 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Vaccines · 2025
    Review
  3. Review
  4. Review
  5. Frontiers in immunology · 2025
    Article
  6. Article
  7. The Bacterial Spore as a Mucosal Vaccine Delivery System.International journal of molecular sciences · 2023
    Review
  8. Review
  9. Article
  10. Review
  11. Cells · 2021
    Article
  12. Article
  13. Application of Bacillus subtilis as a live vaccine vector: A review.The Journal of veterinary medical science · 2020
    Review
  14. Article
  15. Review
  16. Review
  17. Mucosal Delivery of Fusion Proteins withFrontiers in immunology · 2018
    Article
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 4 institutions in 2 countries.

Guangyu Zhaoa State Key Laboratory of Pathogen and Biosecurity; Beijing Institute of Microbiology and Epidemiology ; Beijing , China.
Yu Miao
Yan Guo
Hongjie Qiu
Shihui Sun
Zhihua Kou
Hong Yu
Junfeng Li
Yue Chen
Shibo Jiang
Lanying Du
Yusen Zhou
Institute of Microbiology · CNNew York Proton Center · USShanghai Medical College of Fudan University · CNUniversity of Pittsburgh · US

Funding

B. subtilis spore-delivered M2e-FP-based mucosal universal influenza vaccinesR21AI111152 · NIAID · NEW YORK BLOOD CENTER · PI DU, LANYING · 2014 to 2015
$470k
NIAID NIH HHS R21 AI111152NIAID NIH HHS R21AI111152
6 · The paper itself

Abstract

Highly conserved ectodomain of influenza virus M2 protein (M2e) is an important target for the development of universal influenza vaccines. Today, the use of chemical or genetic fusion constructs have been undertaken to overcome the low immunogenicity of M2e in vaccine formulation. However, current M2e vaccines are neither orally delivered nor heat-stable. In this study, we evaluated the immune efficacy of an orally delivered recombinant M2e vaccine containing 3 molcules of M2e consensus sequence of influenza A viruses, termed RSM2e3. To accomplish this, CotB, a spore coat of Bacillus subtilis (B. subtilis), was used as a fusion partner, and heat-stable nonpathogenic B. subtilis spores were used as the carrier. Our results showed that CotB-M2e3 fusion had no effect on spore structure or function in the resultant recombinant RSM2e3 strain and that heterologous influenza virus M2e protein was successfully displayed on the surface of the recombinant RSM2e3 spore. Importantly, recombinant RSM2e3 spores elicited strong and long-term M2e-specific systemic and mucosal immune responses, completely protecting immunized mice from lethal challenge of A/PR/8/34(H1N1) influenza virus. Taken together, our study forms a solid basis for the development of a novel orally delivered and heat-stable influenza vaccine based on B. subtilis spore surface display.

Indexed as

Administration, OralAnimalsBacillus subtilisBacterial ProteinsFemaleInfluenza A Virus, H1N1 SubtypeInfluenza VaccinesMiceMice, Inbred BALB CRecombinant Fusion ProteinsSpores, BacterialVaccines, SyntheticViral Matrix ProteinsViroporin ProteinsBacterial ProteinsCotB protein, Bacillus subtilisInfluenza VaccinesM2 protein, Influenza A virusRecombinant Fusion ProteinsVaccines, SyntheticViral Matrix ProteinsViroporin ProteinsADCC, antibody-dependent cell-mediated cytotoxicitybacillus subtilisCDC, complement-dependent cytotoxicityCPE, cytopathic effectIAVs, influenza A virusesinfluenza virusM2eM2e, ectodomain of influenza virus M2 proteinsporessurface display

Identifiers

PMID25483702
PMCPMC4514050
OpenAlexW2024106506

What OpenQuestion holds

Textmetadata
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.