Evidence map›Paper›PMID 28982051›Full record

ArticleBiomaterials2017

Active immunotherapy for TNF-mediated inflammation using self-assembled peptide nanofibers.

Carolina Mora-Solano, Yi Wen, Huifang Han, Jianjun Chen, Anita S Chong, Michelle L Miller, Rebecca R Pompano, Joel H Collier

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

40 citing papers in PubMed, 76 citations in OpenAlex.

  1. Article
  2. Article
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  4. Review
  5. Article
  6. Supramolecular Peptide Self-Assemblies Facilitate Oral Immunization.ACS biomaterials science & engineering · 2024
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Self-assembling peptides as immunomodulatory biomaterials.Frontiers in bioengineering and biotechnology · 2023
    Review
  15. The Potential of Vouacapanes fromAdvanced pharmaceutical bulletin · 2023
    Article
  16. Article
  17. Article
  18. Article
  19. Leveraging the therapeutic, biological, and self-assembling potential of peptides for the treatment of viral infections.Journal of controlled release : official journal of the Controlled Release Society · 2022
    Review
  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

8 authors at 2 institutions in 1 country.

Carolina Mora-SolanoDepartment of Surgery, University of Chicago, Chicago, IL, 60637, United States; Molecular Pathogenesis Program, University of Chicago, Chicago, IL, 60637, United States.
Yi WenDepartment of Surgery, University of Chicago, Chicago, IL, 60637, United States.
Huifang HanDepartment of Surgery, University of Chicago, Chicago, IL, 60637, United States.
Jianjun ChenDepartment of Surgery, University of Chicago, Chicago, IL, 60637, United States.
Anita S ChongDepartment of Surgery, University of Chicago, Chicago, IL, 60637, United States.
Michelle L MillerMolecular Pathogenesis Program, University of Chicago, Chicago, IL, 60637, United States.
Rebecca R PompanoDepartment of Chemistry, University of Virginia, Charlottesville, VA, 22904, United States.
Joel H CollierDepartment of Surgery, University of Chicago, Chicago, IL, 60637, United States; Molecular Pathogenesis Program, University of Chicago, Chicago, IL, 60637, United States. Electronic address: joel.collier@duke.edu.
University of Chicago · USUniversity of Virginia · US

Funding

Modular Self-Assembled Coatings for BiomaterialsR01EB009701 · NIBIB · UNIVERSITY OF CHICAGO · PI COLLIER, JOEL H · 2009 to 2021
$4.3M
Supramolecular nanofiber vaccinesR01AI118182 · NIAID · UNIVERSITY OF CHICAGO · PI CHONG, ANITA S, COLLIER, JOEL H · 2015 to 2019
$3.1M
Modular Biomaterials for Targeted Anti-Cytokine ImmunotherapiesR21AR066244 · NIAMS · UNIVERSITY OF CHICAGO · PI COLLIER, JOEL H · 2014 to 2015
$379k
NIAID NIH HHS R01 AI118182NIAMS NIH HHS R21 AR066244NIBIB NIH HHS R01 EB009701
6 · The paper itself

Abstract

Active immunotherapies raising antibody responses against autologous targets are receiving increasing interest as alternatives to the administration of manufactured antibodies. The challenge in such an approach is generating protective and adjustable levels of therapeutic antibodies while at the same time avoiding strong T cell responses that could lead to autoimmune reactions. Here we demonstrate the design of an active immunotherapy against TNF-mediated inflammation using short synthetic peptides that assemble into supramolecular peptide nanofibers. Immunization with these materials, without additional adjuvants, was able to break B cell tolerance and raise protective antibody responses against autologous TNF in mice. The strength of the anti-TNF antibody response could be tuned by adjusting the epitope content in the nanofibers, and the T-cell response was focused on exogenous and non-autoreactive T-cell epitopes. Immunization with unadjuvanted peptide nanofibers was therapeutic in a lethal model of acute inflammation induced by intraperitoneally delivered lipopolysaccharide, whereas formulations adjuvanted with CpG showed comparatively poorer protection that correlated with a more Th1-polarized response. Additionally, immunization with peptide nanofibers did not diminish the ability of mice to clear infections of Listeria monocytogenes. Collectively this work suggests that synthetic self-assembled peptides can be attractive platforms for active immunotherapies against autologous targets.

Indexed as

AnimalsAntibodies, MonoclonalAntibody FormationBacterial VaccinesB-LymphocytesDrug DiscoveryEpitopesFemaleImmunotherapy, ActiveInflammationLipopolysaccharidesListeriosisMice, Inbred C57BLNanofibersParticle SizePeptidesAntibodies, MonoclonalBacterial VaccinesEpitopesLipopolysaccharidesPeptidesTumor Necrosis Factor-alphaVaccines, SubunitActive immunotherapyAdjuvant-freeSupramolecularTNFVaccine

Identifiers

PMID28982051
PMCPMC5716349
OpenAlexW2758624951

What OpenQuestion holds

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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.