Fine Tuning and Efficient T Cell Activation with Stimulatory aCD3 Nanoarrays
Author(s) -
Jovana Matić,
Janosch Deeg,
Alexander Scheffold,
Itamar Goldstein,
Joachim P. Spatz
Publication year - 2013
Publication title -
nano letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.853
H-Index - 488
eISSN - 1530-6992
pISSN - 1530-6984
DOI - 10.1021/nl4022623
Subject(s) - nanotechnology , materials science , cell growth , downregulation and upregulation , ligand (biochemistry) , cell , biophysics , chemistry , receptor , biology , biochemistry , gene
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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