Evidence map›Paper›PMID 28116870›Full record

ArticleAdvanced healthcare materials2017

Multicomponent Injectable Hydrogels for Antigen-Specific Tolerogenic Immune Modulation.

Catia S Verbeke, Susana Gordo, David A Schubert, Sarah A Lewin, Rajiv M Desai, Jessica Dobbins, Kai W Wucherpfennig, David J Mooney

Abstract read
In one paragraph

Article in Advanced healthcare materials, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
9.7field-weighted citation impact, top 1% 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

54 citing papers in PubMed, 95 citations in OpenAlex.

  1. Review
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  11. Unlocking Transplant Tolerance with Biomaterials.Advanced healthcare materials · 2025
    Review
  12. Innovative Hydrogel Design: Tailoring Immunomodulation for Optimal Chronic Wound Recovery.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  13. Biomaterial-Based In Situ Cancer Vaccines.Advanced materials (Deerfield Beach, Fla.) · 2024
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Biomaterial Strategies for Selective Immune Tolerance: Advances and Gaps.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    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.

Catia S VerbekeSchool of Engineering and Applied Sciences, Harvard University, Cambridge, MA, 02138, USA.
Susana GordoDana Farber Cancer Institute, Boston, MA, 02215, USA.
David A SchubertDana Farber Cancer Institute, Boston, MA, 02215, USA.
Sarah A LewinWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, 02115, USA.
Rajiv M DesaiSchool of Engineering and Applied Sciences, Harvard University, Cambridge, MA, 02138, USA.
Jessica DobbinsDana Farber Cancer Institute, Boston, MA, 02215, USA.
Kai W WucherpfennigDana Farber Cancer Institute, Boston, MA, 02215, USA.
David J MooneySchool of Engineering and Applied Sciences, Harvard University, Cambridge, MA, 02138, USA.
Dana-Farber Cancer Institute · USHarvard University · US

Funding

TCR recognition of MHC class II peptide compexes in multiple sclerosisP01AI045757 · NIAID · DANA-FARBER CANCER INSTITUTE · PI KUCHROO, VIJAY K., LOVE, JOHN CHRISTOPHER · 1999 to 2017
$22.8M
Impact of MHC Genotype on Ex Vivo T cell Function in Type 1 DiabetesDP3DK097681 · NIDDK · DANA-FARBER CANCER INST · PI LOVE, JOHN CHRISTOPHER, WUCHERPFENNIG, KAI W · 2012 to 2012
$3.9M
Programming dendritic cells in concert with morphagen delivery for periodontal reR01DE019917 · NIDCR · HARVARD UNIVERSITY · PI KAWAI, TOSHIHISA, MOONEY, DAVID J · 2009 to 2013
$3.5M
NIAID NIH HHS P01 AI045757NIDCR NIH HHS R01 DE019917NIDDK NIH HHS DP3 DK097681
6 · The paper itself

Abstract

Biomaterial scaffolds that enrich and modulate immune cells in situ can form the basis for potent immunotherapies to elicit immunity or reëstablish tolerance. Here, the authors explore the potential of an injectable, porous hydrogel to induce a regulatory T cell (Treg) response by delivering a peptide antigen to dendritic cells in a noninflammatory context. Two methods are described for delivering the BDC peptide from pore-forming alginate gels in the nonobese diabetic mouse model of type 1 diabetes: encapsulation in poly(lactide-co-glycolide) (PLG) microparticles, or direct conjugation to the alginate polymer. While particle-based delivery leads to antigen-specific T cells responses in vivo, PLG particles alter the phenotype of the cells infiltrating the gels. Following gel-based peptide delivery, transient expansion of endogenous antigen-specific T cells is observed in the draining lymph nodes. Antigen-specific T cells accumulate in the gels, and, strikingly, ≈60% of the antigen-specific CD4

Indexed as

AntigensHydrogelsLactic AcidPolyglycolic AcidAnimalsDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1Immune ToleranceMiceMice, Inbred NODPolylactic Acid-Polyglycolic Acid CopolymerT-Lymphocytes, RegulatoryAntigensHydrogelsLactic AcidPolyglycolic AcidPolylactic Acid-Polyglycolic Acid Copolymeralginate hydrogelsantigen-specific tolerancedendritic cellsimmunotherapyregulatory T cells

Identifiers

PMID28116870
PMCPMC5518671
OpenAlexW2580514046

What OpenQuestion holds

Textmetadata
LicenceTDM
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.