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Classification of T-cell activation via autofluorescence lifetime imaging.

Alex J WalshKatherine P MuellerKelsey TweedIsabel JonesChristine M WalshNicole J PiscopoNatalie M NiemiDavid J PagliariniKrishanu SahaMelissa C Skala
Published in: Nature biomedical engineering (2020)
The function of a T cell depends on its subtype and activation state. Here, we show that imaging of the autofluorescence lifetime signals of quiescent and activated T cells can be used to classify the cells. T cells isolated from human peripheral blood and activated in culture using tetrameric antibodies against the surface ligands CD2, CD3 and CD28 showed specific activation-state-dependent patterns of autofluorescence lifetime. Logistic regression models and random forest models classified T cells according to activation state with 97-99% accuracy, and according to activation state (quiescent or activated) and subtype (CD3+CD8+ or CD3+CD4+) with 97% accuracy. Autofluorescence lifetime imaging can be used to non-destructively determine T-cell function.
Keyphrases
  • high resolution
  • peripheral blood
  • endothelial cells
  • oxidative stress
  • cell proliferation
  • fluorescence imaging
  • cell cycle arrest