Evidence map›Paper›PMID 23427254›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

Tuning innate immune activation by surface texturing of polymer microparticles: the role of shape in inflammasome activation.

Christine A Vaine, Milan K Patel, Jintao Zhu, Eunji Lee, Robert W Finberg, Ryan C Hayward, Evelyn A Kurt-Jones

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

33 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. MnOAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Article
  8. Review
  9. Protein and Peptide Nanocluster Vaccines.Current topics in microbiology and immunology · 2021
    Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Biomaterials: Foreign Bodies or Tuners for the Immune Response?International journal of molecular sciences · 2019
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. T cell immunoengineering with advanced biomaterials.Integrative biology : quantitative biosciences from nano to macro · 2017
    Review
  20. 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

7 authors at 2 institutions in 1 country.

Christine A VaineDepartment of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Milan K Patel
Jintao Zhu
Eunji Lee
Robert W Finberg
Ryan C Hayward
Evelyn A Kurt-Jones
University of Massachusetts Chan Medical School · USUniversity of Massachusetts Amherst · US

Funding

PILOT AND FEASIBILITY PROGRAMP30DK032520 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI CZECH, MICHAEL P · 1986 to 2010
$14.6M
Innate Immunity and Herpes Simplex InfectionP01AI083215 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI FINBERG, ROBERT WILLIAM · 2009 to 2010
$3.7M
Innate Immunity Training ProgramT32AI095213 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI SILVERMAN, NEAL · 2011 to 2025
$2.5M
NIAID NIH HHS P01 AI083215NIAID NIH HHS P01 AI083215-01NIAID NIH HHS T32 AI095213NIDDK NIH HHS DK32520NIDDK NIH HHS P30 DK032520
6 · The paper itself

Abstract

Polymeric microparticles have been widely investigated as platforms for delivery of drugs, vaccines, and imaging contrast agents and are increasingly used in a variety of clinical applications. Microparticles activate the inflammasome complex and induce the processing and secretion of IL-1β, a key innate immune cytokine. Recent work suggests that although receptors are clearly important for particle phagocytosis, other physical characteristics, especially shape, play an important role in the way microparticles activate cells. We examined the role of particle surface texturing not only on uptake efficiency but also on the subsequent immune cell activation of the inflammasome. Using a method based on emulsion processing of amphiphilic block copolymers, we prepared microparticles with similar overall sizes and surface chemistries but having either smooth or highly microtextured surfaces. In vivo, textured (budding) particles induced more rapid neutrophil recruitment to the injection site. In vitro, budding particles were more readily phagocytosed than smooth particles and induced more lipid raft recruitment to the phagosome. Remarkably, budding particles also induced stronger IL-1β secretion than smooth particles through activation of the NLRP3 inflammasome. These findings demonstrate a pronounced role of particle surface topography in immune cell activation, suggesting that shape is a major determinant of inflammasome activation.

Indexed as

Immunity, InnatePolymersAnimalsCarrier ProteinsHumansInflammasomesInterleukin-1Interleukin-1betaMacrophagesMembrane MicrodomainsMiceMice, KnockoutNeutrophilsNLR Family, Pyrin Domain-Containing 3 ProteinParticle SizePhagocytosisCarrier ProteinsInflammasomesInterleukin-1Interleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mousePolymers

Identifiers

PMID23427254
PMCPMC3646559
OpenAlexW2154683188

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.