Evidence map›Paper›PMID 29528337›Full record

ArticleThe Journal of clinical investigation2018

Peptide mimic for influenza vaccination using nonnatural combinatorial chemistry.

John J Miles, Mai Ping Tan, Garry Dolton, Emily Sj Edwards, Sarah Ae Galloway, Bruno Laugel, Mathew Clement, Julia Makinde, Kristin Ladell, Katherine K Matthews and 17 more

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–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

20 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. DexDesign: an OSPREY-based algorithm for designing de novo D-peptide inhibitors.Protein engineering, design & selection : PEDS · 2024
    Article
  7. Thioamide Analogues of MHC I Antigen Peptides.Journal of the American Chemical Society · 2023
    Article
  8. D-Peptide and D-Protein Technology: Recent Advances, Challenges, and Opportunities.Chembiochem : a European journal of chemical biology · 2023
    Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors.

John J MilesCentre for Biodiscovery and Molecular Development of Therapeutics, Australian Institute of Tropical Health and Medicine, James Cook University, Cairns, Queensland, Australia.
Mai Ping TanDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
Garry DoltonDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
Emily Sj EdwardsDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
Sarah Ae GallowayDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
Bruno LaugelDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
Mathew ClementDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
Julia MakindeDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
Kristin LadellDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
Katherine K MatthewsQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Thomas S WatkinsQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Katie TungattDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
Yide WongQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Han Siean LeeSchool of Biomedical Sciences, The University of Queensland, Brisbane, Queensland, Australia.
Richard J ClarkSchool of Biomedical Sciences, The University of Queensland, Brisbane, Queensland, Australia.
Johanne M PentierDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
Meriem AttafDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
Anya LissinaDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
Ann AgerDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
Awen GallimoreDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
Pierre J RizkallahDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
Stephanie GrasInfection and Immunity Program and Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, and.
Jamie RossjohnDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
Scott R BurrowsQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
David K ColeDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
David A PriceDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
Andrew K SewellDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.

Funding

Biotechnology and Biological Sciences Research Council BB/H001085/1Cancer Research UK 21200Medical Research Council MR/L008742/1Wellcome Trust
6 · The paper itself

Abstract

Polypeptide vaccines effectively activate human T cells but suffer from poor biological stability, which confines both transport logistics and in vivo therapeutic activity. Synthetic biology has the potential to address these limitations through the generation of highly stable antigenic "mimics" using subunits that do not exist in the natural world. We developed a platform based on D-amino acid combinatorial chemistry and used this platform to reverse engineer a fully artificial CD8+ T cell agonist that mirrored the immunogenicity profile of a native epitope blueprint from influenza virus. This nonnatural peptide was highly stable in human serum and gastric acid, reflecting an intrinsic resistance to physical and enzymatic degradation. In vitro, the synthetic agonist stimulated and expanded an archetypal repertoire of polyfunctional human influenza virus-specific CD8+ T cells. In vivo, specific responses were elicited in naive humanized mice by subcutaneous vaccination, conferring protection from subsequent lethal influenza challenge. Moreover, the synthetic agonist was immunogenic after oral administration. This proof-of-concept study highlights the power of synthetic biology to expand the horizons of vaccine design and therapeutic delivery.

Indexed as

Biomimetic MaterialsInfluenza VaccinesOrthomyxoviridae InfectionsPeptide LibraryVaccinationAnimalsCells, CulturedHumansInfluenza A virusMiceInfluenza VaccinesPeptide LibraryImmunologyInfectious diseaseInfluenzaPeptidesT cells

Identifiers

PMID29528337
PMCPMC5873848

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.