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Author Notes:

Correspondence: Veronika I. Zarnitsyna, Email: veronika.i.zarnitsyna@emory.edu; Rustom Antia, Email: rantia@emory.edu

All co-authors discussed the problem, approach, and results. VZ, AH, and RA formulated the model. VZ ran simulations.

SM, SH, and JK conducted the experimental studies for Figure ​Figure3A.3A. VZ and RA wrote the paper, and all authors approved the final version.

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Subjects:

Research Funding:

SRM, SLH and JEK were supported by NIH R01 HL122559.

VZ and RA were supported by NIH U54 GM111274.

All authors were supported by NIH U19 AI1178918.

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Immunology
  • recall response
  • influenza
  • T cell
  • resident memory
  • central memory
  • A VIRUS-INFECTION
  • CROSS-PROTECTIVE IMMUNITY
  • HETEROSUBTYPIC IMMUNITY
  • NEUTRALIZING EPITOPE
  • LETHAL INFECTION
  • H2 STRAINS
  • B-CELLS
  • MICE
  • ANTIBODIES
  • H1N1

Mathematical Model Reveals the Role of Memory CD8 T Cell Populations in Recall Responses to Influenza

Tools:

Journal Title:

Frontiers in Immunology

Volume:

Volume 7

Publisher:

, Pages 165-165

Type of Work:

Article | Final Publisher PDF

Abstract:

The current influenza vaccine provides narrow protection against the strains included in the vaccine, and needs to be reformulated every few years in response to the constantly evolving new strains. Novel approaches are directed toward developing vaccines that provide broader protection by targeting B and T cell epitopes that are conserved between different strains of the virus. In this paper, we focus on developing mathematical models to explore the CD8 T cell responses to influenza, how they can be boosted, and the conditions under which they contribute to protection. Our models suggest that the interplay between spatial heterogeneity (with the virus infecting the respiratory tract and the immune response being generated in the secondary lymphoid organs) and T cell differentiation (with proliferation occurring in the lymphoid organs giving rise to a subpopulation of resident T cells in the respiratory tract) is the key to understand the dynamics of protection afforded by the CD8 T cell response to influenza. Our results suggest that the time lag for the generation of resident T cells in the respiratory tract and their rate of decay following infection are the key factors that limit the efficacy of CD8 T cell responses. The models predict that an increase in the level of central memory T cells leads to a gradual decrease in the viral load, and, in contrast, there is a sharper protection threshold for the relationship between the size of the population of resident T cells and protection. The models also suggest that repeated natural influenza infections cause the number of central memory CD8 T cells and the peak number of resident memory CD8 T cells to reach their plateaus, and while the former is maintained, the latter decays with time since the most recent infection.

Copyright information:

© 2016 Zarnitsyna, Handel, McMaster, Hayward, Kohlmeier and Antia.

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/).

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