Evidence map›Paper›PMID 37895096›Full record

ArticleInternational journal of molecular sciences2023

Peptide-Decorated Degradable Polycarbonate Nanogels for Eliciting Antigen-Specific Immune Responses.

Judith Stickdorn, Christian Czysch, Carolina Medina-Montano, Lara Stein, Lujuan Xu, Maximilian Scherger, Hansjörg Schild, Stephan Grabbe, Lutz Nuhn

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. 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

9 authors at 4 institutions in 2 countries.

Judith StickdornMax Planck Institute for Polymer Research, 55128 Mainz, Germany.
Christian CzyschMax Planck Institute for Polymer Research, 55128 Mainz, Germany.
Carolina Medina-MontanoDepartment of Dermatology, University Medical Center, Johannes Gutenberg-University Mainz, 55131 Mainz, Germany.
Lara SteinInstitute of Immunology, University Medical Center, Johannes Gutenberg-University Mainz, 55131 Mainz, Germany.
Lujuan XuMax Planck Institute for Polymer Research, 55128 Mainz, Germany.
Maximilian SchergerMax Planck Institute for Polymer Research, 55128 Mainz, Germany.
Hansjörg SchildInstitute of Immunology, University Medical Center, Johannes Gutenberg-University Mainz, 55131 Mainz, Germany.
Stephan GrabbeDepartment of Dermatology, University Medical Center, Johannes Gutenberg-University Mainz, 55131 Mainz, Germany.ORCID 0000-0002-6863-8719
Lutz NuhnMax Planck Institute for Polymer Research, 55128 Mainz, Germany.ORCID 0000-0003-0761-1106
Johannes Gutenberg University Mainz · DEMax Planck Institute for Polymer Research · DEChinese Academy of Sciences · CNUniversity of Würzburg · DE

Funding

Deutsche Forschungsgemeinschaft 213555243Deutsche Forschungsgemeinschaft 417278389Max Buchner Research Foundation 3807National Science Foundation of China 22304181
6 · The paper itself

Abstract

For successful therapeutic interventions in cancer immunotherapy, strong antigen-specific immune responses are required. To this end, immunostimulating cues must be combined with antigens to simultaneously arrive at antigen-presenting cells and initiate cellular immune responses. Recently, imidazoquinolines have shown their vast potential as small molecular Toll-like receptor 7/8 (TLR7/8) agonists for immunostimulation when delivered by nanocarriers. At the same time, peptide antigens are promising antigen candidates but require combination with immune-stimulating adjuvants to boost their immunogenicity and exploit their full potential. Consequently, we herein present biodegradable polycarbonate nanogels as versatile delivery system for adjuvants within the particles' core as well as for peptide antigens by surface decoration. For that purpose, orthogonally addressable multifunctional polycarbonate block copolymers were synthesized, enabling adjuvant conjugation through reactive ester chemistry and peptide decoration by strain-promoted alkyne-azide cycloaddition (SPAAC). In preparation for SPAAC, CD4

Indexed as

NeoplasmsToll-Like Receptor 7Adjuvants, ImmunologicAnimalsAntigensAzidesDendritic CellsHumansImmunityMiceMice, Inbred C57BLNanogelsPeptidesPolycarboxylate CementAdjuvants, ImmunologicAntigensAzidesNanogelsPeptidespolycarbonatePolycarboxylate CementToll-Like Receptor 7aliphatic polycarbonatenanovaccinepeptide antigenpolymer peptide conjugatepost-polymerization modification

Identifiers

PMID37895096
PMCPMC10607756
OpenAlexW4387843801

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.