Differences in circulating γδ T cells in patients with primary colon cancer and relation with prognostic factors.

Downregulation of the T cell system has been proposed as a mechanism to block immunity in colonic cancer (CC). However, little has been studied about circulating αβ and γδ T cells and their immunological status in newly diagnosed patients. The aim of this study was to characterize the αβ and γδ T ce...

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Main Authors: Juan Carlos Andreu-Ballester, Lorena Galindo-Regal, Julia Hidalgo-Coloma, Carmen Cuéllar, Carlos García-Ballesteros, Carolina Hurtado, Natalia Uribe, María Del Carmen Martín, Ana Isabel Jiménez, Francisca López-Chuliá, Antonio Llombart-Cussac
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0243545
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author Juan Carlos Andreu-Ballester
Lorena Galindo-Regal
Julia Hidalgo-Coloma
Carmen Cuéllar
Carlos García-Ballesteros
Carolina Hurtado
Natalia Uribe
María Del Carmen Martín
Ana Isabel Jiménez
Francisca López-Chuliá
Antonio Llombart-Cussac
author_facet Juan Carlos Andreu-Ballester
Lorena Galindo-Regal
Julia Hidalgo-Coloma
Carmen Cuéllar
Carlos García-Ballesteros
Carolina Hurtado
Natalia Uribe
María Del Carmen Martín
Ana Isabel Jiménez
Francisca López-Chuliá
Antonio Llombart-Cussac
author_sort Juan Carlos Andreu-Ballester
collection DOAJ
description Downregulation of the T cell system has been proposed as a mechanism to block immunity in colonic cancer (CC). However, little has been studied about circulating αβ and γδ T cells and their immunological status in newly diagnosed patients. The aim of this study was to characterize the αβ and γδ T cell subsets in peripheral blood of patients with CC matched with healthy volunteers. In this prospective case-control study, blood samples were obtained from 96 patients with newly diagnosed treatment-naïve infiltrating colonic adenocarcinoma and 48 healthy volunteers. Pathological report at surgery was obtained from all CC patients. A significant decrease in CD3+ γδ T cells and CD3+CD8+ γδ T cells (p<0.001) were observed in CC patients. Apoptosis was significantly increased in all conventional and both αβ and γδ T cell subsets in patients with CC vs healthy subjects. γδ T cells were decreased in peripheral blood of patients with microscopic infiltration in tissues, history of cancer and synchronous colon cancer (p < 0.05). IFN-γ was significantly reduced in CC patients compared to controls. Cytotoxic effector γδ T cells TEMRA (CD8 and CD56) are the proportionally most abundant T cells in peripheral blood of CC patients. Patients with CC present a deep downregulation in the systemic T-cell immunity. These variations are evident through all tumor stages and suggest that a deficiency in γδ T cell populations could be preventing control of tumor progression. This fact prove the role of immunomodulation on CC carcinogenesis.
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spelling doaj.art-14ca55c1bfe8437ca9723156c10b873e2022-12-21T19:12:17ZengPublic Library of Science (PLoS)PLoS ONE1932-62032020-01-011512e024354510.1371/journal.pone.0243545Differences in circulating γδ T cells in patients with primary colon cancer and relation with prognostic factors.Juan Carlos Andreu-BallesterLorena Galindo-RegalJulia Hidalgo-ColomaCarmen CuéllarCarlos García-BallesterosCarolina HurtadoNatalia UribeMaría Del Carmen MartínAna Isabel JiménezFrancisca López-ChuliáAntonio Llombart-CussacDownregulation of the T cell system has been proposed as a mechanism to block immunity in colonic cancer (CC). However, little has been studied about circulating αβ and γδ T cells and their immunological status in newly diagnosed patients. The aim of this study was to characterize the αβ and γδ T cell subsets in peripheral blood of patients with CC matched with healthy volunteers. In this prospective case-control study, blood samples were obtained from 96 patients with newly diagnosed treatment-naïve infiltrating colonic adenocarcinoma and 48 healthy volunteers. Pathological report at surgery was obtained from all CC patients. A significant decrease in CD3+ γδ T cells and CD3+CD8+ γδ T cells (p<0.001) were observed in CC patients. Apoptosis was significantly increased in all conventional and both αβ and γδ T cell subsets in patients with CC vs healthy subjects. γδ T cells were decreased in peripheral blood of patients with microscopic infiltration in tissues, history of cancer and synchronous colon cancer (p < 0.05). IFN-γ was significantly reduced in CC patients compared to controls. Cytotoxic effector γδ T cells TEMRA (CD8 and CD56) are the proportionally most abundant T cells in peripheral blood of CC patients. Patients with CC present a deep downregulation in the systemic T-cell immunity. These variations are evident through all tumor stages and suggest that a deficiency in γδ T cell populations could be preventing control of tumor progression. This fact prove the role of immunomodulation on CC carcinogenesis.https://doi.org/10.1371/journal.pone.0243545
spellingShingle Juan Carlos Andreu-Ballester
Lorena Galindo-Regal
Julia Hidalgo-Coloma
Carmen Cuéllar
Carlos García-Ballesteros
Carolina Hurtado
Natalia Uribe
María Del Carmen Martín
Ana Isabel Jiménez
Francisca López-Chuliá
Antonio Llombart-Cussac
Differences in circulating γδ T cells in patients with primary colon cancer and relation with prognostic factors.
PLoS ONE
title Differences in circulating γδ T cells in patients with primary colon cancer and relation with prognostic factors.
title_full Differences in circulating γδ T cells in patients with primary colon cancer and relation with prognostic factors.
title_fullStr Differences in circulating γδ T cells in patients with primary colon cancer and relation with prognostic factors.
title_full_unstemmed Differences in circulating γδ T cells in patients with primary colon cancer and relation with prognostic factors.
title_short Differences in circulating γδ T cells in patients with primary colon cancer and relation with prognostic factors.
title_sort differences in circulating γδ t cells in patients with primary colon cancer and relation with prognostic factors
url https://doi.org/10.1371/journal.pone.0243545
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