TCR down-regulation boosts T-cell-mediated cytotoxicity and protection against poxvirus infections

Ann Kathrine Hansen; Matthias Regner; Charlotte Menne Bonefeld; Lasse Boding; Martin Kongsbak-Wismann; Niels Ødum; Arno Müllbacher; Carsten Geisler; Marina Rode von Essen

doi:10.1002/eji.201141413

TCR down-regulation boosts T-cell-mediated cytotoxicity and protection against poxvirus infections

Ann Kathrine Hansen, Matthias Regner, Charlotte Menne Bonefeld, Lasse Boding, Martin Kongsbak-Wismann, Niels Ødum, Arno Müllbacher, Carsten Geisler, Marina Rode von Essen

8 Citations (Scopus)

Abstract

Cytotoxic T (Tc) cells play a key role in the defense against virus infections. Tc cells recognize infected cells via the T-cell receptor (TCR) and subsequently kill the target cells by one or more cytotoxic mechanisms. Induction of the cytotoxic mechanisms is finely tuned by the activation signals from the TCR. To determine whether TCR down-regulation affects the cytotoxicity of Tc cells, we studied TCR down-regulation-deficient CD3γLLAA mice. We found that Tc cells from CD3γLLAA mice have reduced cytotoxicity due to a specific deficiency in exocytosis of lytic granules. To determine whether this defect was reflected in an increased susceptibility to virus infections, we studied the course of ectromelia virus (ECTV) infection. We found that the susceptibility to ECTV infection was significantly increased in CD3γLLAA mice with a mortality rate almost as high as in granzyme B knock-out mice. Finally, we found that TCR signaling in CD3γLLAA Tc cells caused highly increased tyrosine phosphorylation and activation of the c-Cbl ubiquitin ligase, and that the impaired exocytosis of lytic granules could be rescued by the knockdown of c-Cbl. Thus, our work demonstrates that TCR down-regulation critically increases Tc cell cytotoxicity and protection against poxvirus infection.

Original language	English
Journal	European Journal of Immunology
Volume	41
Issue number	7
Pages (from-to)	1948-1957
Number of pages	10
ISSN	0014-2980
DOIs	https://doi.org/10.1002/eji.201141413
Publication status	Published - Jul 2011

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@article{bc12199f9f964d9d8419a806e42d1942,

title = "TCR down-regulation boosts T-cell-mediated cytotoxicity and protection against poxvirus infections",

abstract = "Cytotoxic T (Tc) cells play a key role in the defense against virus infections. Tc cells recognize infected cells via the T-cell receptor (TCR) and subsequently kill the target cells by one or more cytotoxic mechanisms. Induction of the cytotoxic mechanisms is finely tuned by the activation signals from the TCR. To determine whether TCR down-regulation affects the cytotoxicity of Tc cells, we studied TCR down-regulation-deficient CD3γLLAA mice. We found that Tc cells from CD3γLLAA mice have reduced cytotoxicity due to a specific deficiency in exocytosis of lytic granules. To determine whether this defect was reflected in an increased susceptibility to virus infections, we studied the course of ectromelia virus (ECTV) infection. We found that the susceptibility to ECTV infection was significantly increased in CD3γLLAA mice with a mortality rate almost as high as in granzyme B knock-out mice. Finally, we found that TCR signaling in CD3γLLAA Tc cells caused highly increased tyrosine phosphorylation and activation of the c-Cbl ubiquitin ligase, and that the impaired exocytosis of lytic granules could be rescued by the knockdown of c-Cbl. Thus, our work demonstrates that TCR down-regulation critically increases Tc cell cytotoxicity and protection against poxvirus infection.",

author = "Hansen, {Ann Kathrine} and Matthias Regner and Bonefeld, {Charlotte Menne} and Lasse Boding and Martin Kongsbak-Wismann and Niels {\O}dum and Arno M{\"u}llbacher and Carsten Geisler and {von Essen}, {Marina Rode}",

note = "Copyright {\textcopyright} 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.",

year = "2011",

month = jul,

doi = "10.1002/eji.201141413",

language = "English",

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pages = "1948--1957",

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TY - JOUR

T1 - TCR down-regulation boosts T-cell-mediated cytotoxicity and protection against poxvirus infections

AU - Hansen, Ann Kathrine

AU - Regner, Matthias

AU - Bonefeld, Charlotte Menne

AU - Boding, Lasse

AU - Kongsbak-Wismann, Martin

AU - Ødum, Niels

AU - Müllbacher, Arno

AU - Geisler, Carsten

AU - von Essen, Marina Rode

PY - 2011/7

Y1 - 2011/7

N2 - Cytotoxic T (Tc) cells play a key role in the defense against virus infections. Tc cells recognize infected cells via the T-cell receptor (TCR) and subsequently kill the target cells by one or more cytotoxic mechanisms. Induction of the cytotoxic mechanisms is finely tuned by the activation signals from the TCR. To determine whether TCR down-regulation affects the cytotoxicity of Tc cells, we studied TCR down-regulation-deficient CD3γLLAA mice. We found that Tc cells from CD3γLLAA mice have reduced cytotoxicity due to a specific deficiency in exocytosis of lytic granules. To determine whether this defect was reflected in an increased susceptibility to virus infections, we studied the course of ectromelia virus (ECTV) infection. We found that the susceptibility to ECTV infection was significantly increased in CD3γLLAA mice with a mortality rate almost as high as in granzyme B knock-out mice. Finally, we found that TCR signaling in CD3γLLAA Tc cells caused highly increased tyrosine phosphorylation and activation of the c-Cbl ubiquitin ligase, and that the impaired exocytosis of lytic granules could be rescued by the knockdown of c-Cbl. Thus, our work demonstrates that TCR down-regulation critically increases Tc cell cytotoxicity and protection against poxvirus infection.

AB - Cytotoxic T (Tc) cells play a key role in the defense against virus infections. Tc cells recognize infected cells via the T-cell receptor (TCR) and subsequently kill the target cells by one or more cytotoxic mechanisms. Induction of the cytotoxic mechanisms is finely tuned by the activation signals from the TCR. To determine whether TCR down-regulation affects the cytotoxicity of Tc cells, we studied TCR down-regulation-deficient CD3γLLAA mice. We found that Tc cells from CD3γLLAA mice have reduced cytotoxicity due to a specific deficiency in exocytosis of lytic granules. To determine whether this defect was reflected in an increased susceptibility to virus infections, we studied the course of ectromelia virus (ECTV) infection. We found that the susceptibility to ECTV infection was significantly increased in CD3γLLAA mice with a mortality rate almost as high as in granzyme B knock-out mice. Finally, we found that TCR signaling in CD3γLLAA Tc cells caused highly increased tyrosine phosphorylation and activation of the c-Cbl ubiquitin ligase, and that the impaired exocytosis of lytic granules could be rescued by the knockdown of c-Cbl. Thus, our work demonstrates that TCR down-regulation critically increases Tc cell cytotoxicity and protection against poxvirus infection.

U2 - 10.1002/eji.201141413

DO - 10.1002/eji.201141413

M3 - Journal article

C2 - 21590764

SN - 0014-2980

VL - 41

SP - 1948

EP - 1957

JO - European Journal of Immunology

JF - European Journal of Immunology

IS - 7

ER -

TCR down-regulation boosts T-cell-mediated cytotoxicity and protection against poxvirus infections

Abstract

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