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. 2013 Jul 16;110(29):11833-8.
doi: 10.1073/pnas.1222467110. Epub 2013 Jul 1.

Quorum sensing allows T cells to discriminate between self and nonself

Affiliations

Quorum sensing allows T cells to discriminate between self and nonself

Thomas Charles Butler et al. Proc Natl Acad Sci U S A. .

Abstract

T cells orchestrate pathogen-specific adaptive immune responses by identifying peptides derived from pathogenic proteins that are displayed on the surface of infected cells. Host cells also display peptide fragments from the host's own proteins. Incorrectly identifying peptides derived from the body's own proteome as pathogenic can result in autoimmune disease. To minimize autoreactivity, immature T cells that respond to self-peptides are deleted in the thymus by a process called negative selection. However, negative selection is imperfect, and autoreactive T cells exist in healthy individuals. To understand how autoimmunity is yet avoided, without loss of responsiveness to pathogens, we have developed a model of T-cell training and response. Our model shows that T cells reliably respond to infection and avoid autoimmunity because collective decisions made by the T-cell population, rather than the responses of individual T cells, determine biological outcomes. The theory is qualitatively consistent with experimental data and yields a criterion for thymic selection to be adequate for suppressing autoimmunity.

Keywords: T-cell–mediated autoimmunity; self tolerance; statistical mechanics.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Fig. 1.
Fig. 1.
Schematic representation of the role of a quorum-sensing-like mechanism for T-cell proliferation. Peptides bound to major histocompatibility complex (MHC) molecules on the surface of dendritic cells in the lymph nodes are presented to T cells. If an insufficient number of T cells are activated, no response is generated. If a sufficient number of T cells are activated, proliferation and response result.
Fig. 2.
Fig. 2.
(Upper) Probability distributions for the number of T cells activated by a collection of self-peptides vs. a collection of pathogenic peptides. (Lower) Risk functions for all three kinds of error computed as conditional risks in Eq. 7. An optimal threshold requires more T cells to be activated than are likely to be activated by self but a sufficiently low number that at least the threshold number will essentially always be activated by pathogen. The parameters are formula image, formula image, and formula image.

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