Evidence map›Paper›PMID 28894111›Full record

ArticleScientific reports2017

Induction of high titred, non-neutralising antibodies by self-adjuvanting peptide epitopes derived from the respiratory syncytial virus fusion protein.

Noushin Jaberolansar, Keith J Chappell, Daniel Watterson, Imogen M Bermingham, Istvan Toth, Paul R Young, Mariusz Skwarczynski

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

14 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Current Prospects in Peptide-Based Subunit Nanovaccines.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Respiratory Syncytial Virus Vaccine Approaches: a Current Overview.Current clinical microbiology reports · 2017
    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

7 authors at 1 institution in 1 country.

Noushin JaberolansarSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Queensland, Australia.
Keith J ChappellSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Queensland, Australia. k.chappell@uq.edu.au.
Daniel WattersonSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Queensland, Australia. d.watterson@uq.edu.au.
Imogen M BerminghamSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Queensland, Australia.
Istvan TothSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Queensland, Australia.
Paul R YoungSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Queensland, Australia.
Mariusz SkwarczynskiSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Queensland, Australia. m.skwarczynski@uq.edu.au.
University of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Respiratory syncytial virus (RSV) causes severe lower respiratory tract illness in infants and young children. The significant morbidity and mortality rates associated with RSV infection make an effective RSV vaccine development a priority. Two neutralising antibody binding sites, Ø and II, located on the pre-fusion RSV F glycoprotein are prime candidates for epitope-focused vaccine design. We report on a vaccine strategy that utilises a lipid core peptide (LCP) delivery system with self-adjuvanting properties in conjunction with either the antigenic site Ø or II (B cell epitopes) along with PADRE as a T helper cell epitope. These LCP constructs adopted the desired helical conformation in solution and were recognised by their cognate antibodies D25 and Motavizumab, specific for site Ø and II on RSV F protein, respectively. The LCP constructs were capable of eliciting higher levels of antigen specific antibodies than those induced by antigens administered with complete Freund's adjuvant, demonstrating the potent adjuvanting properties of LCP delivery. However, the antibodies induced failed to recognise native F protein or neutralise virus infectivity. These results provide a note of caution in assuming that peptide vaccines, successfully designed to structurally mimic minimal linear B cell epitopes, will necessarily elicit the desired immune response.

Indexed as

Adjuvants, ImmunologicAnimalsAntibodies, ViralChlorocebus aethiopsCHO CellsCricetulusEnzyme-Linked Immunosorbent AssayEpitopesHumansImmunizationImmunogenicity, VaccineImmunoglobulin GNeutralization TestsPeptidesRecombinant ProteinsRespiratory Syncytial Virus, HumanAdjuvants, ImmunologicAntibodies, ViralEpitopesImmunoglobulin GPeptidesRecombinant ProteinsRespiratory Syncytial Virus VaccinesVaccines, SubunitViral Fusion Proteins

Identifiers

PMID28894111
PMCPMC5593926
OpenAlexW2752879464

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.