Identification of Nascent Memory CD8 T Cells and Modeling of Their Ontogeny

Cell Syst. 2017 Mar 22;4(3):306-317.e4. doi: 10.1016/j.cels.2017.01.014. Epub 2017 Feb 22.

Abstract

Primary immune responses generate short-term effectors and long-term protective memory cells. The delineation of the genealogy linking naive, effector, and memory cells has been complicated by the lack of phenotypes discriminating effector from memory differentiation stages. Using transcriptomics and phenotypic analyses, we identify Bcl2 and Mki67 as a marker combination that enables the tracking of nascent memory cells within the effector phase. We then use a formal approach based on mathematical models describing the dynamics of population size evolution to test potential progeny links and demonstrate that most cells follow a linear naive→early effector→late effector→memory pathway. Moreover, our mathematical model allows long-term prediction of memory cell numbers from a few early experimental measurements. Our work thus provides a phenotypic means to identify effector and memory cells, as well as a mathematical framework to investigate their genealogy and to predict the outcome of immunization regimens in terms of memory cell numbers generated.

Keywords: CD8 T cell differentiation; CD8 memory T cell ontogeny; differential equations; dynamical modeling; predictive tool; vaccine design.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • B-Lymphocyte Subsets / classification
  • Biological Ontologies
  • CD8-Positive T-Lymphocytes / cytology*
  • CD8-Positive T-Lymphocytes / physiology*
  • Cell Differentiation / immunology
  • Cell Line
  • Immunologic Memory / immunology*
  • Ki-67 Antigen / physiology
  • Lymphocyte Activation / immunology
  • Mice
  • Mice, Inbred C57BL
  • Models, Theoretical
  • Phenotype
  • Proto-Oncogene Proteins c-bcl-2

Substances

  • Ki-67 Antigen
  • MKI67 protein, human
  • Proto-Oncogene Proteins c-bcl-2