Evidence map›Paper›PMID 20080728›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2010

A self-assembling peptide acting as an immune adjuvant.

Jai S Rudra, Ye F Tian, Jangwook P Jung, Joel H Collier

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 214 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
214citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 3% 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

214 citing papers in PubMed, 1 synthesis or guideline pooled it, 513 citations in OpenAlex.

  1. Controlling timing and location in vaccines.Advanced drug delivery reviews · 2020
    Pooled it
  2. Article
  3. Review
  4. Article
  5. Precise Regulation of Membrane Proteins: From Physical Technology to Biomolecular Strategy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
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  7. Review
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  20. Organoid scaffold materials: research and application.Frontiers in bioengineering and biotechnology · 2025
    Review

154 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 1 country.

Jai S RudraDepartment of Surgery and Committee on Molecular Medicine, University of Chicago, 5841 S Maryland Avenue, Chicago, IL 60637, USA.
Ye F Tian
Jangwook P Jung
Joel H Collier
University of Chicago · USIllinois Institute of Technology · US

Funding

Modular Self-Assembled Coatings for BiomaterialsR01EB009701 · NIBIB · UNIVERSITY OF CHICAGO · PI COLLIER, JOEL H · 2009 to 2021
$4.3M
Designing ECM-Inspired Peptide Biomaterials for Regenerative MedicineR21DE017703 · NIDCR · UNIVERSITY OF CINCINNATI · PI COLLIER, JOEL H · 2006 to 2007
$422k
Modular Biomaterials for Cell Sheet RegenerationR21EB007335 · NIBIB · UNIVERSITY OF CINCINNATI · PI COLLIER, JOEL H · 2007 to 2008
$421k
NIBIB NIH HHS 1R01EB009701NIBIB NIH HHS 7R21EB007335NIBIB NIH HHS R01 EB009701NIBIB NIH HHS R21 EB007335NIDCR NIH HHS R21 DE017703NIDCR NIH HHS R21DE017703
6 · The paper itself

Abstract

The development of vaccines and other immunotherapies has been complicated by heterogeneous antigen display and the use of incompletely defined immune adjuvants with complex mechanisms of action. We have observed strong antibody responses in mice without the coadministration of any additional adjuvant by noncovalently assembling a T and B cell epitope peptide into nanofibers using a short C-terminal peptide extension. Self-assembling peptides have been explored recently as scaffolds for tissue engineering and regenerative medicine, but our results indicate that these materials may also be useful as chemically defined adjuvants. In physiological conditions, these peptides self-assembled into long, unbranched fibrils that displayed the epitope on their surfaces. IgG1, IgG2a, and IgG3 were raised against epitope-bearing fibrils in levels similar to the epitope peptide delivered in complete Freund's adjuvant (CFA), and IgM production was even greater for the self-assembled epitope. This response was dependent on self-assembly, and the self-assembling sequence was not immunogenic by itself, even when delivered in CFA. Undetectable levels of interferon-gamma, IL-2, and IL-4 in cultures of peptide-challenged splenocytes from immunized mice suggested that the antibody responses did not involve significant T cell help.

Indexed as

Adjuvants, ImmunologicAmino Acid SequenceAnimalsB-LymphocytesEnzyme-Linked Immunosorbent AssayEpitopesFreund's AdjuvantImmunoglobulin GImmunotherapyMiceModels, MolecularMolecular Sequence DataNanofibersOvalbuminPeptide FragmentsProtein ConformationAdjuvants, ImmunologicEpitopesFreund's AdjuvantImmunoglobulin GOvalbuminPeptide Fragments

Identifiers

PMID20080728
PMCPMC2818904
OpenAlexW2092328303

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.