Evidence map›Paper›PMID 29124929›Full record

ArticleACS nano2017

Injectable Polymeric Cytokine-Binding Nanowires Are Effective Tissue-Specific Immunomodulators.

Colin R Zamecnik, Margaret M Lowe, David M Patterson, Michael D Rosenblum, Tejal A Desai

Open access · greenAbstract read
In one paragraph

Article in ACS nano, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. NK cell-based tumor immunotherapy.Bioactive materials · 2024
    Review
  5. Article
  6. Harnessing Biomaterials for Immunomodulatory-Driven Tissue Engineering.Regenerative engineering and translational medicine · 2023
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. TiOACS biomaterials science & engineering · 2020
    Article
  12. 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

5 authors at 1 institution in 1 country.

Colin R ZamecnikDepartment of Bioengineering and Therapeutic Sciences, University of California , San Francisco, California 94158, United States.ORCID 0000-0002-9477-1388
Margaret M LoweDepartment of Dermatology, University of California San Francisco , San Francisco, California 94143, United States.
David M PattersonDepartment of Pharmaceutical Chemistry, University of California San Francisco , San Francisco, California 94143, United States.
Michael D RosenblumDepartment of Dermatology, University of California San Francisco , San Francisco, California 94143, United States.
Tejal A DesaiDepartment of Bioengineering and Therapeutic Sciences, University of California , San Francisco, California 94158, United States.
University of California, San Francisco · US

Funding

Research BaseP30DK063720 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GERMAN, MICHAEL S · 2003 to 2019
$21.8M
MOLECULAR AND CELLULAR IMMUNOLOGYT32AI007334 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CYSTER, JASON G · 1988 to 2023
$11.0M
Functional Manipulation of Memory Regulatory T cells in SkinDP2AR068130 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ROSENBLUM, MICHAEL DAVID · 2014 to 2014
$2.4M
Mechanisms of nanostructure-enhanced transepithelial drug deliveryR01EB018842 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DESAI, TEJAL A. · 2014 to 2017
$1.4M
NIAID NIH HHS T32 AI007334NIAMS NIH HHS DP2 AR068130NIBIB NIH HHS R01 EB018842NIDDK NIH HHS P30 DK063720
6 · The paper itself

Abstract

Injectable nanomaterials that interact with the host immune system without surgical intervention present spatially anchored complements to cell transplantation and could offer improved pharmacokinetics compared to systemic cytokine therapy. Here we demonstrate fabrication of high aspect ratio polycaprolactone nanowires coupled with cytokine-binding antibodies that assemble into porous matrices when injected into the subcutaneous space. These structures are fabricated using a nanotemplating technique that allows for tunability of particle dimensions and utilize a straightforward maleimide conjugation chemistry to allow site-specific coupling to proteins. Nanowires are well tolerated in vivo and incite minimal inflammatory infiltrate. Nanowires conjugated with antibodies were designed to capture and potentiate endogenous interleukin-2 (IL-2), an important leukocyte activating cytokine. Together these nanowire-antibody matrices were capable of localizing endogenous IL-2 in the skin and activated targeted specific natural killer and T cell subsets, demonstrating both tissue- and cell-specific immune activation. These self-assembling nanowire matrices show promise as scaffolds to present engineered, local receptor-ligand interactions for cytokine-mediated disease.

Indexed as

AnimalsAntibodiesFemaleHumansImmunologic FactorsInjections, SubcutaneousInterleukin-2MaleimidesMice, Inbred C57BLNanocompositesNanowiresOrgan SpecificityParticle SizePolyestersT-LymphocytesAntibodiesImmunologic FactorsInterleukin-2MaleimidespolycaprolactonePolyesterscytokinesimmunomodulationinterleukin-2nanotechnologypolycaprolactoneS4B6-1

Identifiers

PMID29124929
PMCPMC5709211
OpenAlexW2767420271

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.