Dangerous γδ T cells in aged mice

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Dangerous γδ T cells in aged mice. / Prinz, Immo; Sandrock, Inga.

In: EMBO REP, Vol. 20, No. 8, 08.2019, p. e48678.

Research output: SCORING: Contribution to journalSCORING: Review articleResearch

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@article{ff58e3ac6e5f4439a07f948ab11b53b0,
title = "Dangerous γδ T cells in aged mice",
abstract = "Progressive susceptibility to tumors and infectious diseases in the elderly are a serious threat to public health in aging societies. For this reason, there is growing interest in mechanisms and predictive biomarkers that accompany and potentially cause this process. In this issue of EMBO Reports, Chen et al [1] report the surprising finding that a specific subset of γδ T cells with very limited clonal diversity strongly expands in lymph nodes of aging mice. These T cells uniformly express a T-cell receptor (TCR) composed of a Vγ6 and a Vδ1 chain and show an effector T-cell phenotype characterized by the swift production of the pro-inflammatory cytokine interleukin-17 (IL-17) upon ex vivo stimulation (γδT17 cells). Since γδT17 cells are suspected to be pro-tumorigenic [2], the authors next compared how mice of different age coped with an experimental lung cancer challenge and found impaired anti-tumor responses in old mice. Based on these observations, they propose a link between changes of the composition of γδ T cells in the aging lymph nodes and increased risk of cancer development in aged mice.",
keywords = "Animals, Interleukin-7, Lymph Nodes, Mice, Neoplasms, Receptors, Antigen, T-Cell, gamma-delta, T-Lymphocytes",
author = "Immo Prinz and Inga Sandrock",
note = "{\textcopyright} 2019 The Authors.",
year = "2019",
month = aug,
doi = "10.15252/embr.201948678",
language = "English",
volume = "20",
pages = "e48678",
journal = "EMBO REP",
issn = "1469-221X",
publisher = "NATURE PUBLISHING GROUP",
number = "8",

}

RIS

TY - JOUR

T1 - Dangerous γδ T cells in aged mice

AU - Prinz, Immo

AU - Sandrock, Inga

N1 - © 2019 The Authors.

PY - 2019/8

Y1 - 2019/8

N2 - Progressive susceptibility to tumors and infectious diseases in the elderly are a serious threat to public health in aging societies. For this reason, there is growing interest in mechanisms and predictive biomarkers that accompany and potentially cause this process. In this issue of EMBO Reports, Chen et al [1] report the surprising finding that a specific subset of γδ T cells with very limited clonal diversity strongly expands in lymph nodes of aging mice. These T cells uniformly express a T-cell receptor (TCR) composed of a Vγ6 and a Vδ1 chain and show an effector T-cell phenotype characterized by the swift production of the pro-inflammatory cytokine interleukin-17 (IL-17) upon ex vivo stimulation (γδT17 cells). Since γδT17 cells are suspected to be pro-tumorigenic [2], the authors next compared how mice of different age coped with an experimental lung cancer challenge and found impaired anti-tumor responses in old mice. Based on these observations, they propose a link between changes of the composition of γδ T cells in the aging lymph nodes and increased risk of cancer development in aged mice.

AB - Progressive susceptibility to tumors and infectious diseases in the elderly are a serious threat to public health in aging societies. For this reason, there is growing interest in mechanisms and predictive biomarkers that accompany and potentially cause this process. In this issue of EMBO Reports, Chen et al [1] report the surprising finding that a specific subset of γδ T cells with very limited clonal diversity strongly expands in lymph nodes of aging mice. These T cells uniformly express a T-cell receptor (TCR) composed of a Vγ6 and a Vδ1 chain and show an effector T-cell phenotype characterized by the swift production of the pro-inflammatory cytokine interleukin-17 (IL-17) upon ex vivo stimulation (γδT17 cells). Since γδT17 cells are suspected to be pro-tumorigenic [2], the authors next compared how mice of different age coped with an experimental lung cancer challenge and found impaired anti-tumor responses in old mice. Based on these observations, they propose a link between changes of the composition of γδ T cells in the aging lymph nodes and increased risk of cancer development in aged mice.

KW - Animals

KW - Interleukin-7

KW - Lymph Nodes

KW - Mice

KW - Neoplasms

KW - Receptors, Antigen, T-Cell, gamma-delta

KW - T-Lymphocytes

U2 - 10.15252/embr.201948678

DO - 10.15252/embr.201948678

M3 - SCORING: Review article

C2 - 31286651

VL - 20

SP - e48678

JO - EMBO REP

JF - EMBO REP

SN - 1469-221X

IS - 8

ER -