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Cross-reactivity00:42

Cross-reactivity

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Quantifying T Cell Cross-Reactivity: Influenza and Coronaviruses.

Jessica Ann Gaevert1,2, Daniel Luque Duque3, Grant Lythe3

  • 1Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.

Viruses
|September 28, 2021
PubMed
Summary
This summary is machine-generated.

Viral cross-reactivity, where T cells recognize similar epitopes, can boost immunity. This pre-existing immunity is crucial for adaptive immune responses to influenza and coronaviruses.

Keywords:
bipartite networkcompetition processcross-reactivityheterologous infectionmathematical modelingpre-existing immunity

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Area of Science:

  • Immunology
  • Computational Biology
  • Virology

Background:

  • Cross-reactive T cells can provide protection against different viral strains.
  • Pre-existing immunity is vital for adaptive immune responses to influenza and coronaviruses.
  • T cell recognition patterns can be modeled using bipartite networks.

Purpose of the Study:

  • To model T cell cross-reactivity using bipartite networks.
  • To explore the dynamics of T cell repertoires during infection and re-infection.
  • To quantify T cell cross-reactivity based on epitope similarity.

Main Methods:

  • Constructing bipartite networks to represent T cell epitope recognition.
  • Analyzing T cell repertoire dynamics under various conditions (homeostasis, infection, re-infection).
  • Introducing a circular epitope space to measure cross-reactivity quantitatively.

Main Results:

  • Bipartite networks can effectively model T cell cross-reactivity.
  • Structural similarity of epitopes drives cross-reactivity, alongside chance occurrences.
  • T cell cross-reactivity is a quantitative measure of epitope overlap within the defined space.

Conclusions:

  • T cell cross-reactivity is a significant factor in adaptive immunity against viruses like influenza and coronaviruses.
  • Bipartite network modeling provides a framework for understanding T cell repertoire dynamics.
  • Quantifying epitope overlap enhances our understanding of cross-protective immune responses.