Investigating the Dynamics of MCMV-Specific CD8+ T Cell Responses in Individual Hosts

Front Immunol. 2019 Jun 19:10:1358. doi: 10.3389/fimmu.2019.01358. eCollection 2019.

Abstract

Infection by Cytomegalovirus (CMV) is characterized by the massive expansion and continued maintenance of CMV-specific CD8+ T cells for certain CMV-derived peptides. This phenomenon called "memory inflation" has made CMV a primary target for the generation of T cell based vaccine vectors against various diseases. However, many aspects concerning the generation and maintenance of the inflationary CD8+ T cell response still remain to be resolved. In this study, we combined experimental data and mathematical models to analyze the dynamics of circulatory inflationary CD8+ T cells within individual mice infected by MCMV. Obtaining frequent measurements on the number and frequency of CMV-specific CD8+ T cells up to 70 days post infection, we find that mathematical models assuming differing viral stimuli during acute infection and the inflationary phase provide a better description for the observed dynamics than models relying on similar viral stimuli during both phases. In addition, our analysis allowed a detailed quantification of the different phases of memory inflation within individual mice (1st-expansion - contraction - 2nd expansion/maintenance) indicating remarkable consistency of the timing of these phases across mice, but considerable variation in the size of the individual responses between mice. Our analysis provides a first step toward generating a mechanistic framework for analyzing the generation and maintenance of inflationary CD8+ T cells while accounting for individual heterogeneity. Extending these analyses by incorporating measurements from additional compartments and more prolonged sampling will help to obtain a systematic and quantitative understanding of the factors regulating the process of memory inflation.

Keywords: CD8+ T cells; MCMV-infection; individual dynamics; mathematical modeling; memory inflation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Algorithms
  • Animals
  • Antigens, Viral / immunology
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / metabolism
  • Epitopes, T-Lymphocyte / immunology
  • Herpesviridae Infections / immunology*
  • Herpesviridae Infections / metabolism
  • Herpesviridae Infections / virology*
  • Host-Pathogen Interactions / immunology*
  • Immunologic Memory
  • Lymphocyte Activation / drug effects
  • Mice
  • Models, Biological
  • Muromegalovirus / immunology*
  • T-Cell Antigen Receptor Specificity*
  • Viral Load
  • Virus Activation / immunology

Substances

  • Antigens, Viral
  • Epitopes, T-Lymphocyte