Evidence map›Paper›PMID 27849050›Full record

ArticleScientific reports2016

Employing Escherichia coli-derived outer membrane vesicles as an antigen delivery platform elicits protective immunity against Acinetobacter baumannii infection.

Weiwei Huang, Shijie Wang, Yufeng Yao, Ye Xia, Xu Yang, Kui Li, Pengyan Sun, Cunbao Liu, Wenjia Sun, Hongmei Bai and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

68 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Data-driven Atlas ofFrontiers in cellular and infection microbiology · 2026
    Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Outer membrane vesicles fromFrontiers in molecular biosciences · 2025
    Article
  10. Proteomic analysis of outer membrane vesicles derived from the type A5 Strain ofFrontiers in cellular and infection microbiology · 2025
    Article
  11. Review
  12. Review
  13. Genetically surface-modifiedBiotechnology reports (Amsterdam, Netherlands) · 2024
    Article
  14. Article
  15. Review
  16. Loss of Lipooligosaccharide Synthesis inInternational journal of molecular sciences · 2024
    Article
  17. Review
  18. Review
  19. Review
  20. Outer Membrane Vesicle Vaccine Platforms.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2024
    Review

8 more citing papers are in PubMed but not listed here.

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.

Weiwei HuangLaboratory of Molecular Immunology, Institute of Medical Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Kunming, 650118, China.
Shijie WangLaboratory of Molecular Immunology, Institute of Medical Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Kunming, 650118, China.
Yufeng YaoLaboratory of Molecular Immunology, Institute of Medical Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Kunming, 650118, China.
Ye XiaLaboratory of Molecular Immunology, Institute of Medical Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Kunming, 650118, China.
Xu YangLaboratory of Molecular Immunology, Institute of Medical Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Kunming, 650118, China.
Kui LiLaboratory of Molecular Immunology, Institute of Medical Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Kunming, 650118, China.
Pengyan SunLaboratory of Molecular Immunology, Institute of Medical Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Kunming, 650118, China.
Cunbao LiuLaboratory of Molecular Immunology, Institute of Medical Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Kunming, 650118, China.
Wenjia SunLaboratory of Molecular Immunology, Institute of Medical Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Kunming, 650118, China.
Hongmei BaiLaboratory of Molecular Immunology, Institute of Medical Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Kunming, 650118, China.
Xiaojie ChuLaboratory of Molecular Immunology, Institute of Medical Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Kunming, 650118, China.
Yang LiLaboratory of Molecular Immunology, Institute of Medical Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Kunming, 650118, China.
Yanbing MaLaboratory of Molecular Immunology, Institute of Medical Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Kunming, 650118, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Outer membrane vesicles (OMVs) have proven to be highly immunogenic and induced an immune response against bacterial infection in human clinics and animal models. We sought to investigate whether engineered OMVs can be a feasible antigen-delivery platform for efficiently inducing specific antibody responses. In this study, Omp22 (an outer membrane protein of A. baumannii) was displayed on E. coli DH5α-derived OMVs (Omp22-OMVs) using recombinant gene technology. The morphological features of Omp22-OMVs were similar to those of wild-type OMVs (wtOMVs). Immunization with Omp22-OMVs induced high titers of Omp22-specific antibodies. In a murine sepsis model, Omp22-OMV immunization significantly protected mice from lethal challenge with a clinically isolated A. baumannii strain, which was evidenced by the increased survival rate of the mice, the reduced bacterial burdens in the lung, spleen, liver, kidney, and blood, and the suppressed serum levels of inflammatory cytokines. In vitro opsonophagocytosis assays showed that antiserum collected from Omp22-OMV-immunized mice had bactericidal activity against clinical isolates, which was partly specific antibody-dependent. These results strongly indicated that engineered OMVs could display a whole heterologous protein (~22 kDa) on the surface and effectively induce specific antibody responses, and thus OMVs have the potential to be a feasible vaccine platform.

Indexed as

Acinetobacter baumanniiAcinetobacter InfectionsAmino Acid SequenceAnimalsAntibodies, BacterialAntigensBacterial Outer Membrane ProteinsBacterial VaccinesBase SequenceEscherichia coliFemaleImmunizationMice, Inbred ICRSepsisSequence Homology, Amino AcidSequence Homology, Nucleic AcidAntibodies, BacterialAntigensBacterial Outer Membrane ProteinsBacterial Vaccines

Identifiers

PMID27849050
PMCPMC5110958

What OpenQuestion holds

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Registered trials

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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.