Evidence map›Paper›PMID 24351757›Full record

ArticleClinical and vaccine immunology : CVI2014

Multiepitope fusion antigen induces broadly protective antibodies that prevent adherence of Escherichia coli strains expressing colonization factor antigen I (CFA/I), CFA/II, and CFA/IV.

Xiaosai Ruan, David E Knudsen, Katie M Wollenberg, David A Sack, Weiping Zhang

Open access · diamondAbstract read
In one paragraph

Article in Clinical and vaccine immunology : CVI, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

39 citing papers in PubMed, 47 citations in OpenAlex.

  1. Applied and environmental microbiology · 2026
    Article
  2. Review
  3. Review
  4. Recent progress in enterotoxigenicInfection and immunity · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Characterization ofApplied and environmental microbiology · 2025
    Article
  9. Article
  10. Mapping the functional B-cell epitopes ofApplied and environmental microbiology · 2024
    Article
  11. Article
  12. A broadly immunogenic polyvalentInfection and immunity · 2023
    Article
  13. Article
  14. Article
  15. A polyvalent multiepitope protein cross-protects againstProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  16. Evaluation of Multivalent EnterotoxigenicApplied and environmental microbiology · 2022
    Article
  17. Article
  18. Article
  19. Article
  20. 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

5 authors at 2 institutions in 1 country.

Xiaosai RuanVeterinary and Biomedical Sciences Department, The Center for Infectious Disease Research and Vaccinology, South Dakota State University, Brookings, South Dakota, USA.
David E Knudsen
Katie M Wollenberg
David A Sack
Weiping Zhang
South Dakota State University · USJohns Hopkins University · US

Funding

Determining vaccine candidacy of LT and STa toxoid fusions against enterotoxigeniR21AI083897 · NIAID · SOUTH DAKOTA STATE UNIVERSITY · PI ZHANG, WEIPING · 2009 to 2010
$368k
NIAID NIH HHS AI083897NIAID NIH HHS R21 AI083897
6 · The paper itself

Abstract

Diarrhea is the second leading cause of death in children younger than 5 years and continues to be a major threat to global health. Enterotoxigenic Escherichia coli (ETEC) strains are the most common bacteria causing diarrhea in developing countries. ETEC strains are able to attach to host small intestinal epithelial cells by using bacterial colonization factor antigen (CFA) adhesins. This attachment helps to initiate the diarrheal disease. Vaccines that induce antiadhesin immunity to block adherence of ETEC strains that express immunologically heterogeneous CFA adhesins are expected to protect against ETEC diarrhea. In this study, we created a CFA multiepitope fusion antigen (MEFA) carrying representative epitopes of CFA/I, CFA/II (CS1, CS2, and CS3), and CFA/IV (CS4, CS5, and CS6), examined its immunogenicity in mice, and assessed the potential of this MEFA as an antiadhesin vaccine against ETEC. Mice intraperitoneally immunized with this CFA MEFA exhibited no adverse effects and developed immune responses to CFA/I, CFA/II, and CFA/IV adhesins. Moreover, after incubation with serum of the immunized mice, ETEC or E. coli strains expressing CFA/I, CFA/II, or CFA/IV adhesins were significantly inhibited in adherence to Caco-2 cells. Our results indicated this CFA MEFA elicited antibodies that not only cross-reacted to CFA/I, CFA/II and CFA/IV adhesins but also broadly inhibited adherence of E. coli strains expressing these seven adhesins and suggested that this CFA MEFA could be a candidate to induce broad-spectrum antiadhesin protection against ETEC diarrhea. Additionally, this antigen construction approach (creating an MEFA) may be generally used in vaccine development against heterogenic pathogens.

Indexed as

AnimalsAntibodies, BacterialBacterial AdhesionCaco-2 CellsColicinsDiarrheaEnterotoxigenic Escherichia coliEpithelial CellsEpitopesEscherichia coli InfectionsEscherichia coli VaccinesFemaleFimbriae ProteinsHumansMiceMice, Inbred C57BLAntibodies, Bacterialcolicin 5 protein, E coliColicinscolonization factor antigensEpitopesEscherichia coli VaccinesFimbriae ProteinsRecombinant Fusion ProteinsVaccines, Synthetic

Identifiers

PMID24351757
PMCPMC3910947
OpenAlexW2171782036

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.