Aging augments obesity-induced thymic involution and peripheral T cell exhaustion altering the "obesity paradox"
Aging augments obesity-induced thymic involution and peripheral T cell exhaustion altering the "obesity paradox"
INTRODUCTION: The incidence of obesity, a condition characterized by systemic chronic inflammation, has reached pandemic proportions and is a poor prognostic factor in many pathologic states. However, its role on immune parameters has been diverse and at times contradictory. We have previously demonstrated that obesity can result in what has been called the "obesity paradox" which results in increased T cell exhaustion, but also greater efficacy of immune checkpoint blockade in cancer treatment.
METHODS: The role of obesity, particularly in the context of aging, has not been robustly explored using preclinical models. We therefore evaluated how age impacts the immune environment on T cell development and function using diet-induced obese (DIO) mice.
RESULTS: We observed that DIO mice initially displayed greater thymopoiesis but then developed greater thymic involution over time compared to their lean counterparts. Both aging and obesity resulted in increased T cell memory conversion combined with increased expression of T cell exhaustion markers and Treg expansion. This increased T cell immunosuppression with age then resulted in a loss of anti-tumor efficacy by immune checkpoint inhibitors (ICIs) in older DIO mice compared to the younger DIO counterparts.
DISCUSSION: These results suggest that both aging and obesity contribute to T cell dysfunction resulting in increased thymic involution. This combined with increased T cell exhaustion and immunosuppressive parameters affects immunotherapy efficacy reducing the advantage of obesity in cancer immunotherapy responses.
Mice, Animals, Thymus Gland, T-Cell Exhaustion, Aging, Obesity, Cell Differentiation, Mice, Obese
1012016
Vick, Logan V
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Collins, Craig P
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Khuat, Lam T
ca00b1c8-4f0e-4f61-bb1a-493f120cef8e
Wang, Ziming
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Dunai, Cordelia
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Aguilar, Ethan G
556396ca-71bc-484b-87bd-8282da13d787
Stoffel, Kevin
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Yendamuri, Sai
4807b269-424e-4c05-aa09-8b0d3f1ec6af
Smith, Randall
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Mukherjee, Sarbajit
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Barbi, Joseph
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Canter, Robert J
edec6c77-358e-4fdf-ac7d-4252842efdfe
Monjazeb, Arta M
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Murphy, William J
290fec7b-1d9f-4d5d-80f3-4154fda8970c
26 January 2023
Vick, Logan V
793cbb3e-8fd9-47a5-922b-45baae4919bb
Collins, Craig P
57337558-437d-41ac-beb4-8e9febeaa023
Khuat, Lam T
ca00b1c8-4f0e-4f61-bb1a-493f120cef8e
Wang, Ziming
d67e406a-af5b-444c-af42-08dab6d8df28
Dunai, Cordelia
28579a87-d6e5-4ba0-abd3-900e8cdfff98
Aguilar, Ethan G
556396ca-71bc-484b-87bd-8282da13d787
Stoffel, Kevin
2fc986ca-dbb7-4c9e-a3cb-7e5c4212b340
Yendamuri, Sai
4807b269-424e-4c05-aa09-8b0d3f1ec6af
Smith, Randall
e2b8881b-bd2e-41ff-9f38-eea180431241
Mukherjee, Sarbajit
818f7293-36fa-4e16-95b6-03078db7030d
Barbi, Joseph
c90514ee-1d29-4748-9f5a-5a41f142328a
Canter, Robert J
edec6c77-358e-4fdf-ac7d-4252842efdfe
Monjazeb, Arta M
904b7fcb-fcfa-49ab-906c-599c4fa7582f
Murphy, William J
290fec7b-1d9f-4d5d-80f3-4154fda8970c
Vick, Logan V, Collins, Craig P, Khuat, Lam T, Wang, Ziming, Dunai, Cordelia, Aguilar, Ethan G, Stoffel, Kevin, Yendamuri, Sai, Smith, Randall, Mukherjee, Sarbajit, Barbi, Joseph, Canter, Robert J, Monjazeb, Arta M and Murphy, William J
(2023)
Aging augments obesity-induced thymic involution and peripheral T cell exhaustion altering the "obesity paradox".
Frontiers in Immunology, 13, .
(doi:10.3389/fimmu.2022.1012016).
Abstract
INTRODUCTION: The incidence of obesity, a condition characterized by systemic chronic inflammation, has reached pandemic proportions and is a poor prognostic factor in many pathologic states. However, its role on immune parameters has been diverse and at times contradictory. We have previously demonstrated that obesity can result in what has been called the "obesity paradox" which results in increased T cell exhaustion, but also greater efficacy of immune checkpoint blockade in cancer treatment.
METHODS: The role of obesity, particularly in the context of aging, has not been robustly explored using preclinical models. We therefore evaluated how age impacts the immune environment on T cell development and function using diet-induced obese (DIO) mice.
RESULTS: We observed that DIO mice initially displayed greater thymopoiesis but then developed greater thymic involution over time compared to their lean counterparts. Both aging and obesity resulted in increased T cell memory conversion combined with increased expression of T cell exhaustion markers and Treg expansion. This increased T cell immunosuppression with age then resulted in a loss of anti-tumor efficacy by immune checkpoint inhibitors (ICIs) in older DIO mice compared to the younger DIO counterparts.
DISCUSSION: These results suggest that both aging and obesity contribute to T cell dysfunction resulting in increased thymic involution. This combined with increased T cell exhaustion and immunosuppressive parameters affects immunotherapy efficacy reducing the advantage of obesity in cancer immunotherapy responses.
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Published date: 26 January 2023
Additional Information:
Copyright © 2023 Vick, Collins, Khuat, Wang, Dunai, Aguilar, Stoffel, Yendamuri, Smith, Mukherjee, Barbi, Canter, Monjazeb and Murphy.
Keywords:
Mice, Animals, Thymus Gland, T-Cell Exhaustion, Aging, Obesity, Cell Differentiation, Mice, Obese
Identifiers
Local EPrints ID: 495500
URI: http://eprints.soton.ac.uk/id/eprint/495500
ISSN: 1664-3224
PURE UUID: 6eabb3ed-260b-40ec-8c43-8c10f1056dc3
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Date deposited: 14 Nov 2024 18:10
Last modified: 19 Dec 2024 03:09
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Contributors
Author:
Logan V Vick
Author:
Craig P Collins
Author:
Lam T Khuat
Author:
Ziming Wang
Author:
Cordelia Dunai
Author:
Ethan G Aguilar
Author:
Kevin Stoffel
Author:
Sai Yendamuri
Author:
Randall Smith
Author:
Sarbajit Mukherjee
Author:
Joseph Barbi
Author:
Robert J Canter
Author:
Arta M Monjazeb
Author:
William J Murphy
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