Evidence map›Paper›PMID 32973764›Full record

ArticleFrontiers in immunology2020

Multifactorial Design of a Supramolecular Peptide Anti-IL-17 Vaccine Toward the Treatment of Psoriasis.

Lucas S Shores, Sean H Kelly, Kelly M Hainline, Jutamas Suwanpradid, Amanda S MacLeod, Joel H Collier

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

23 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  8. Supramolecular Peptide Self-Assemblies Facilitate Oral Immunization.ACS biomaterials science & engineering · 2024
    Article
  9. Article
  10. Review
  11. Article
  12. Article
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  14. Article
  15. Challenges and Future Trends in the Treatment of Psoriasis.International journal of molecular sciences · 2023
    Review
  16. Article
  17. Article
  18. Review
  19. Review
  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

6 authors at 1 institution in 1 country.

Lucas S ShoresDepartment of Biomedical Engineering, Duke University, Durham, NC, United States.
Sean H KellyDepartment of Biomedical Engineering, Duke University, Durham, NC, United States.
Kelly M HainlineDepartment of Biomedical Engineering, Duke University, Durham, NC, United States.
Jutamas SuwanpradidDepartment of Dermatology, Duke University School of Medicine, Durham, NC, United States.
Amanda S MacLeodDepartment of Dermatology, Duke University School of Medicine, Durham, NC, United States.
Joel H CollierDepartment of Biomedical Engineering, Duke University, Durham, NC, United States.
Duke University · US

Funding

Modular Self-Assembled Coatings for BiomaterialsR01EB009701 · NIBIB · UNIVERSITY OF CHICAGO · PI COLLIER, JOEL H · 2009 to 2021
$4.3M
ERBB KINASE ACTIVATION AND TRANSFORMATIONR01CA039207 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI KUNG, HSING-JIEN · 1986 to 2004
$1.5M
NCI NIH HHS R01 CA039207NIBIB NIH HHS R01 EB009701
6 · The paper itself

Abstract

Current treatments for chronic immune-mediated diseases such as psoriasis, rheumatoid arthritis, or Crohn's disease commonly rely on cytokine neutralization using monoclonal antibodies; however, such approaches have drawbacks. Frequent repeated dosing can lead to the formation of anti-drug antibodies and patient compliance issues, and it is difficult to identify a single antibody that is broadly efficacious across diverse patient populations. As an alternative to monoclonal antibody therapy, anti-cytokine immunization is a potential means for long-term therapeutic control of chronic inflammatory diseases. Here we report a supramolecular peptide-based approach for raising antibodies against IL-17 and demonstrate its efficacy in a murine model of psoriasis. B-cell epitopes from IL-17 were co-assembled with the universal T-cell epitope PADRE using the Q11 self-assembling peptide nanofiber system. These materials, with or without adjuvants, raised antibody responses against IL-17. Exploiting the modularity of the system, multifactorial experimental designs were used to select formulations maximizing titer and avidity. In a mouse model of psoriasis induced by imiquimod, unadjuvanted nanofibers had therapeutic efficacy, which could be enhanced with alum adjuvant but reversed with CpG adjuvant. Measurements of antibody subclass induced by adjuvanted and unadjuvanted formulations revealed strong correlations between therapeutic efficacy and titers of IgG1 (improved efficacy) or IgG2b (worsened efficacy). These findings have important implications for the development of anti-cytokine active immunotherapies and suggest that immune phenotype is an important metric for eliciting therapeutic anti-cytokine antibody responses.

Indexed as

Drug DesignAnimalsDisease Models, AnimalFemaleImmunotherapy, ActiveInterleukin-17MiceMice, Inbred C57BLPsoriasisVaccines, SubunitInterleukin-17Vaccines, Subunitactive immunotherapyanti-cytokineimmunoengineeringinflammatory diseasesself-assembly

Identifiers

PMID32973764
PMCPMC7461889
OpenAlexW3057782889

What OpenQuestion holds

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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.