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Fine tuning and efficient T cell activation with stimulatory aCD3 nano-arrays

MPG-Autoren
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Matic,  Jovana
Cellular Biophysics, Max Planck Institute for Medical Research, Max Planck Society;
Biophysical Chemistry, Institute of Physical Chemistry, University of Heidelberg, 69120 Heidelberg, Germany;

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Deeg,  Janosch
Cellular Biophysics, Max Planck Institute for Medical Research, Max Planck Society;
Biophysical Chemistry, Institute of Physical Chemistry, University of Heidelberg, 69120 Heidelberg, Germany;

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Spatz,  Joachim P.
Cellular Biophysics, Max Planck Institute for Medical Research, Max Planck Society;
Biophysical Chemistry, Institute of Physical Chemistry, University of Heidelberg, 69120 Heidelberg, Germany;

Externe Ressourcen

http://pubs.acs.org/doi/pdf/10.1021/nl4022623
(beliebiger Volltext)

https://dx.doi.org/10.1021/nl4022623
(beliebiger Volltext)

http://pubs.acs.org/doi/suppl/10.1021/nl4022623
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Zitation

Matic, J., Deeg, J., Scheffold, A., Goldstein, I., & Spatz, J. P. (2013). Fine tuning and efficient T cell activation with stimulatory aCD3 nano-arrays. Nano Letters, 13(11), 5090-5097. doi:10.1021/nl4022623.


Zitierlink: https://hdl.handle.net/11858/00-001M-0000-0015-1009-B
Zusammenfassung
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.