Fine tuning and efficient T cell activation with stimulatory aCD3 nanoarrays

Anti-CD3 (aCD3) nanoarrays fabricated by self-assembled nanopatterning combined with site-directed protein immobilization techniques represent a novel T cell stimulatory platform that allows tight control over ligand orientation and surface density. Here, we show that activation of primary human CD4...

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Bibliographic Details
Main Authors: Matić, Jovana (Author) , Deeg, Janosch A. (Author) , Scheffold, Alexander (Author) , Goldstein, Itamar (Author) , Spatz, Joachim P. (Author)
Format: Article (Journal)
Language:English
Published: October 10, 2013
In: Nano letters
Year: 2013, Volume: 13, Issue: 11, Pages: 5090-5097
ISSN:1530-6992
DOI:10.1021/nl4022623
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/nl4022623
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Author Notes:Jovana Matic, Janosch Deeg, Alexander Scheffold, Itamar Goldstein, and Joachim P. Spatz
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Summary:Anti-CD3 (aCD3) nanoarrays fabricated by self-assembled nanopatterning combined with site-directed protein immobilization techniques represent a novel T cell stimulatory platform that allows tight control over ligand orientation and surface density. Here, we show that activation of primary human CD4+ T cells, defined by CD69 upregulation, IL-2 production and cell proliferation, correlates with aCD3 density on nanoarrays. Immobilization of aCD3 through nanopatterning had two effects: cell activation was significantly higher on these surfaces than on aCD3-coated plastics and allowed unprecedented fine-tuning of T cell response.
Item Description:Gesehen am 25.06.2021
Physical Description:Online Resource
ISSN:1530-6992
DOI:10.1021/nl4022623