Peripheral self-reactivity regulates antigen-specific CD8 T-cell responses and cell division under physiological conditions

T-cell identity is established by the expression of a clonotypic T-cell receptor (TCR), generated by somatic rearrangement of TCRα and β genes. The properties of the TCR determine both the degree of self-reactivity and the repertoire of antigens that can be recognized. For CD8 T cells, the relations...

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Main Authors: Lee Kim Swee, Zhen Wei Tan, Anna Sanecka, Nagisa Yoshida, Harshil Patel, Gijsbert Grotenbreg, Eva-Maria Frickel, Hidde L. Ploegh
Format: Article
Language:English
Published: The Royal Society 2016-01-01
Series:Open Biology
Subjects:
Online Access:https://royalsocietypublishing.org/doi/pdf/10.1098/rsob.160293
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author Lee Kim Swee
Zhen Wei Tan
Anna Sanecka
Nagisa Yoshida
Harshil Patel
Gijsbert Grotenbreg
Eva-Maria Frickel
Hidde L. Ploegh
author_facet Lee Kim Swee
Zhen Wei Tan
Anna Sanecka
Nagisa Yoshida
Harshil Patel
Gijsbert Grotenbreg
Eva-Maria Frickel
Hidde L. Ploegh
author_sort Lee Kim Swee
collection DOAJ
description T-cell identity is established by the expression of a clonotypic T-cell receptor (TCR), generated by somatic rearrangement of TCRα and β genes. The properties of the TCR determine both the degree of self-reactivity and the repertoire of antigens that can be recognized. For CD8 T cells, the relationship between TCR identity—hence reactivity to self—and effector function(s) remains to be fully understood and has rarely been explored outside of the H-2b haplotype. We measured the affinity of three structurally distinct CD8 T-cell-derived TCRs that recognize the identical H-2 Ld-restricted epitope, derived from the Rop7 protein of Toxoplasma gondii. We used CD8 T cells obtained from mice generated by somatic cell nuclear transfer as the closest approximation of primary T cells with physiological TCR rearrangements and TCR expression levels. First, we demonstrate the common occurrence of secondary rearrangements in endogenously rearranged loci. Furthermore, we characterized and compared the response of Rop7-specific CD8 T-cell clones upon Toxoplasma gondii infection as well as effector function and TCR signalling upon antigenic stimulation in vitro. Antigen-independent TCR cross-linking in vitro uncovered profound intrinsic differences in the effector functions between T-cell clones. Finally, by assessing the degree of self-reactivity and comparing the transcriptomes of naive Rop7 CD8 T cells, we show that lower self-reactivity correlates with lower effector capacity, whereas higher self-reactivity is associated with enhanced effector function as well as cell cycle entry under physiological conditions. Altogether, our data show that potential effector functions and basal proliferation of CD8 T cells are set by self-reactivity thresholds.
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spelling doaj.art-66b62db06e24433da7a409fcf108233e2022-12-21T23:05:34ZengThe Royal SocietyOpen Biology2046-24412016-01-0161110.1098/rsob.160293160293Peripheral self-reactivity regulates antigen-specific CD8 T-cell responses and cell division under physiological conditionsLee Kim SweeZhen Wei TanAnna SaneckaNagisa YoshidaHarshil PatelGijsbert GrotenbregEva-Maria FrickelHidde L. PloeghT-cell identity is established by the expression of a clonotypic T-cell receptor (TCR), generated by somatic rearrangement of TCRα and β genes. The properties of the TCR determine both the degree of self-reactivity and the repertoire of antigens that can be recognized. For CD8 T cells, the relationship between TCR identity—hence reactivity to self—and effector function(s) remains to be fully understood and has rarely been explored outside of the H-2b haplotype. We measured the affinity of three structurally distinct CD8 T-cell-derived TCRs that recognize the identical H-2 Ld-restricted epitope, derived from the Rop7 protein of Toxoplasma gondii. We used CD8 T cells obtained from mice generated by somatic cell nuclear transfer as the closest approximation of primary T cells with physiological TCR rearrangements and TCR expression levels. First, we demonstrate the common occurrence of secondary rearrangements in endogenously rearranged loci. Furthermore, we characterized and compared the response of Rop7-specific CD8 T-cell clones upon Toxoplasma gondii infection as well as effector function and TCR signalling upon antigenic stimulation in vitro. Antigen-independent TCR cross-linking in vitro uncovered profound intrinsic differences in the effector functions between T-cell clones. Finally, by assessing the degree of self-reactivity and comparing the transcriptomes of naive Rop7 CD8 T cells, we show that lower self-reactivity correlates with lower effector capacity, whereas higher self-reactivity is associated with enhanced effector function as well as cell cycle entry under physiological conditions. Altogether, our data show that potential effector functions and basal proliferation of CD8 T cells are set by self-reactivity thresholds.https://royalsocietypublishing.org/doi/pdf/10.1098/rsob.160293cd8 t cellsself-affinitycell cycle
spellingShingle Lee Kim Swee
Zhen Wei Tan
Anna Sanecka
Nagisa Yoshida
Harshil Patel
Gijsbert Grotenbreg
Eva-Maria Frickel
Hidde L. Ploegh
Peripheral self-reactivity regulates antigen-specific CD8 T-cell responses and cell division under physiological conditions
Open Biology
cd8 t cells
self-affinity
cell cycle
title Peripheral self-reactivity regulates antigen-specific CD8 T-cell responses and cell division under physiological conditions
title_full Peripheral self-reactivity regulates antigen-specific CD8 T-cell responses and cell division under physiological conditions
title_fullStr Peripheral self-reactivity regulates antigen-specific CD8 T-cell responses and cell division under physiological conditions
title_full_unstemmed Peripheral self-reactivity regulates antigen-specific CD8 T-cell responses and cell division under physiological conditions
title_short Peripheral self-reactivity regulates antigen-specific CD8 T-cell responses and cell division under physiological conditions
title_sort peripheral self reactivity regulates antigen specific cd8 t cell responses and cell division under physiological conditions
topic cd8 t cells
self-affinity
cell cycle
url https://royalsocietypublishing.org/doi/pdf/10.1098/rsob.160293
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