Evidence map›Paper›PMID 24667098›Full record

ReviewCurrent opinion in biotechnology2014

Microbial biosynthesis of designer outer membrane vesicles.

Jenny L Baker, Linxiao Chen, Joseph A Rosenthal, David Putnam, Matthew P DeLisa

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in biotechnology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
7.4field-weighted citation impact, top 2% 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

50 citing papers in PubMed, 94 citations in OpenAlex.

  1. Article
  2. Bacterial Outer Membrane Vesicles in Potentiating Cancer Vaccines: Progress and Prospects.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  3. Article
  4. A distinct subpopulation of membrane vesicles inApplied and environmental microbiology · 2025
    Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Tailoring biomaterials for vaccine delivery.Journal of nanobiotechnology · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Role ofFrontiers in microbiology · 2023
    Review
  19. Article
  20. 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

5 authors at 1 institution in 1 country.

Jenny L BakerSchool of Chemical and Biomolecular Engineering, Cornell University, Ithaca, NY 14853, USA.
Linxiao ChenSchool of Chemical and Biomolecular Engineering, Cornell University, Ithaca, NY 14853, USA.
Joseph A RosenthalDepartment of Biomedical Engineering, Cornell University, Ithaca, NY 14853, USA.
David PutnamSchool of Chemical and Biomolecular Engineering, Cornell University, Ithaca, NY 14853, USA; Department of Biomedical Engineering, Cornell University, Ithaca, NY 14853, USA. Electronic address: dap43@cornell.edu.
Matthew P DeLisaSchool of Chemical and Biomolecular Engineering, Cornell University, Ithaca, NY 14853, USA; Department of Biomedical Engineering, Cornell University, Ithaca, NY 14853, USA. Electronic address: matthew.delisa@cornell.edu.
Cornell University · US

Funding

Engineered Outer Membrane Vesicles as DNA Vaccine Delivery VehiclesR21EB005669 · NIBIB · CORNELL UNIVERSITY · PI PUTNAM, DAVID A · 2006 to 2007
$398k
NIBIB NIH HHS R21 EB005669
6 · The paper itself

Abstract

Outer membrane vesicles (OMVs) are nanoscale proteoliposomes that are ubiquitously secreted by Gram-negative bacteria. Interest in these bioparticles has escalated over the years, leading to discoveries regarding their composition, production, and vaccine potential. Given that many steps in vesicle biogenesis are 'engineerable,' it is now possible to tailor OMVs for specific applications. Such tailoring involves modifying the OMV-producing bacterium through protein, pathway, or genome engineering in a manner that specifically alters the final OMV product. For example, targeted deletion or upregulation of genes associated with the cell envelope can modulate vesicle production or remodel the composition of vesicle components such as lipopolysaccharide. Likewise, bacteria can be reprogrammed to incorporate heterologously expressed proteins into either the membrane or lumenal compartment of OMVs. We anticipate that further research in the field of OMV engineering will enable continued design and biosynthesis of specialized vesicles for numerous biotechnological purposes ranging from the delivery of vaccines to the deconstruction of cellulosic substrates.

Indexed as

AnimalsBacteriaBioengineeringBiological TransportCell MembraneHumans

Identifiers

PMID24667098
PMCPMC4171203
OpenAlexW1987245161

What OpenQuestion holds

Textmetadata
LicenceTDM
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.