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Fine Tuning and Efficient T Cell Activation with Stimulatory aCD3 Nanoarrays

[Image: see text] 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...

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Autores principales: Matic, Jovana, Deeg, Janosch, Scheffold, Alexander, Goldstein, Itamar, Spatz, Joachim P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2013
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834297/
https://www.ncbi.nlm.nih.gov/pubmed/24111628
http://dx.doi.org/10.1021/nl4022623
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author Matic, Jovana
Deeg, Janosch
Scheffold, Alexander
Goldstein, Itamar
Spatz, Joachim P.
author_facet Matic, Jovana
Deeg, Janosch
Scheffold, Alexander
Goldstein, Itamar
Spatz, Joachim P.
author_sort Matic, Jovana
collection PubMed
description [Image: see text] 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.
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spelling pubmed-38342972013-11-22 Fine Tuning and Efficient T Cell Activation with Stimulatory aCD3 Nanoarrays Matic, Jovana Deeg, Janosch Scheffold, Alexander Goldstein, Itamar Spatz, Joachim P. Nano Lett [Image: see text] 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. American Chemical Society 2013-10-10 2013-11-13 /pmc/articles/PMC3834297/ /pubmed/24111628 http://dx.doi.org/10.1021/nl4022623 Text en Copyright © 2013 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle Matic, Jovana
Deeg, Janosch
Scheffold, Alexander
Goldstein, Itamar
Spatz, Joachim P.
Fine Tuning and Efficient T Cell Activation with Stimulatory aCD3 Nanoarrays
title Fine Tuning and Efficient T Cell Activation with Stimulatory aCD3 Nanoarrays
title_full Fine Tuning and Efficient T Cell Activation with Stimulatory aCD3 Nanoarrays
title_fullStr Fine Tuning and Efficient T Cell Activation with Stimulatory aCD3 Nanoarrays
title_full_unstemmed Fine Tuning and Efficient T Cell Activation with Stimulatory aCD3 Nanoarrays
title_short Fine Tuning and Efficient T Cell Activation with Stimulatory aCD3 Nanoarrays
title_sort fine tuning and efficient t cell activation with stimulatory acd3 nanoarrays
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834297/
https://www.ncbi.nlm.nih.gov/pubmed/24111628
http://dx.doi.org/10.1021/nl4022623
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