Evidence map›Paper›PMID 36377878›Full record

ArticleMicrobiology spectrum2022

Oral Immunization with Attenuated

Guodong Zhou, Yichen Tian, Jiashuo Tian, Qifeng Ma, Shan Huang, Quan Li, Shifeng Wang, Huoying Shi

Open access · goldAbstract read
In one paragraph

Article in Microbiology spectrum, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Design of an oral vaccine againstThe veterinary quarterly · 2026
    Article
  2. Article
  3. Evaluation ofInfection and immunity · 2025
    Article
  4. Review
  5. TheFrontiers in cellular and infection microbiology · 2025
    Article
  6. Review
  7. Review
  8. Chimeric proteins of Mycoplasma hyopneumoniae as vaccine and preclinical model for immunological evaluation.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2024
    Article
  9. A subunit vaccine based on P97R1, P46, P42, and P65 fromFrontiers in veterinary science · 2024
    Article
  10. Article
  11. 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 2 institutions in 2 countries.

Guodong ZhouCollege of Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu, China.
Yichen TianCollege of Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu, China.
Jiashuo TianCollege of Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu, China.
Qifeng MaCollege of Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu, China.
Shan HuangCollege of Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu, China.
Quan LiCollege of Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu, China.
Shifeng WangDepartment of Infectious Diseases and Immunology, College of Veterinary Medicine, University of Floridagrid.15276.37, Gainesville, Florida, USA.
Huoying ShiCollege of Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu, China.ORCID 0000-0003-4128-329X
Yangzhou University · CNUniversity of Florida · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mycoplasma hyopneumoniae (M. hyopneumoniae, Mhp) is the etiological agent of swine enzootic pneumonia (EP), which has been associated with considerable economic losses due to reduced daily weight gain and feed efficiency. Adhesion to the cilia is important for Mhp to colonize the respiratory epithelium. Therefore, a successful vaccine must induce broad Mhp-specific immune responses at the mucosal surface. Recombinant attenuated Salmonella strains are believed to act as powerful live vaccine vectors that are able to elicit mucosal immune responses against various pathogens. To develop efficacious and inexpensive vaccines against Mhp, the immune responses and protection induced by recombinant attenuated Salmonella vaccines based on the P42 and P97 antigens of Mhp were evaluated. In general, the oral inoculation of recombinant rSC0016(pS-P42) or rSC0016(pS-P97) resulted in strong mucosal immunity, cell-mediated immunity, and humoral immunity, which was a mixed Th1/Th2-type response. In addition, the levels of specific IL-4 and IFN-γ in the immunized mice were increased, and the proliferation of lymphocytes was also enhanced, confirming the production of a good cellular immune response. Finally, both vaccine candidate strains were able to improve the weight loss of mice after a challenge and reduce clinical symptoms, lung pathological damage, and the inflammatory cell infiltration. These results suggest that the delivery of protective antigens with recombinant attenuated Salmonella vectors may be an effective means by which to combat Mhp infection.

Indexed as

Mycoplasma hyopneumoniaePneumonia of Swine, MycoplasmalSalmonella entericaAnimalsBacterial VaccinesImmunity, MucosalImmunizationMiceSalmonellaSwineVaccines, SyntheticBacterial VaccinesVaccines, SyntheticMycoplasma hyopneumoniaeP42P97recombinant vaccineSalmonella Choleraesuis

Identifiers

PMID36377878
PMCPMC9769600
OpenAlexW4309097087

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.