Type 1 Innate Lymphoid Cells Limit the Antitumoral Immune Response

Natural killer (NK) cells are known to be able to kill established tumor cell lines, but important caveats remain regarding their roles in the detection and elimination of developing primary tumors. Using a genetic model of selective ILC1 and NK cell deficiency, we showed that these cells were dispe...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Margaux Vienne, Marion Etiennot, Bertrand Escalière, Justine Galluso, Lionel Spinelli, Sophie Guia, Aurore Fenis, Eric Vivier, Yann M. Kerdiles
Formato: article
Lenguaje:EN
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://doaj.org/article/5d93b170ef1f4e6eba648775277a2912
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:5d93b170ef1f4e6eba648775277a2912
record_format dspace
spelling oai:doaj.org-article:5d93b170ef1f4e6eba648775277a29122021-11-16T07:47:13ZType 1 Innate Lymphoid Cells Limit the Antitumoral Immune Response1664-322410.3389/fimmu.2021.768989https://doaj.org/article/5d93b170ef1f4e6eba648775277a29122021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fimmu.2021.768989/fullhttps://doaj.org/toc/1664-3224Natural killer (NK) cells are known to be able to kill established tumor cell lines, but important caveats remain regarding their roles in the detection and elimination of developing primary tumors. Using a genetic model of selective ILC1 and NK cell deficiency, we showed that these cells were dispensable for tumor immunosurveillance and immunoediting in the MCA-induced carcinogenesis model. However, we were able to generate primary cell lines derived from MCA-induced tumors with graded sensitivity to NK1.1+ cells (including NK cells and ILC1). This differential sensitivity was associated neither with a modulation of intratumoral NK cell frequency, nor the capacity of tumor cells to activate NK cells. Instead, ILC1 infiltration into the tumor was found to be a critical determinant of NK1.1+ cell-dependent tumor growth. Finally, bulk tumor RNAseq analysis identified a gene expression signature associated with tumor sensitivity to NK1.1+ cells. ILC1 therefore appear to play an active role in inhibiting the antitumoral immune response, prompting to evaluate the differential tumor infiltration of ILC1 and NK cells in patients to optimize the harnessing of immunity in cancer therapies.Margaux VienneMarion EtiennotBertrand EscalièreJustine GallusoLionel SpinelliSophie GuiaAurore FenisEric VivierEric VivierEric VivierYann M. KerdilesFrontiers Media S.A.articleinnateinnate lymphoid cells (ILCs)antitumoral immunityNK cellsILC1Immunologic diseases. AllergyRC581-607ENFrontiers in Immunology, Vol 12 (2021)
institution DOAJ
collection DOAJ
language EN
topic innate
innate lymphoid cells (ILCs)
antitumoral immunity
NK cells
ILC1
Immunologic diseases. Allergy
RC581-607
spellingShingle innate
innate lymphoid cells (ILCs)
antitumoral immunity
NK cells
ILC1
Immunologic diseases. Allergy
RC581-607
Margaux Vienne
Marion Etiennot
Bertrand Escalière
Justine Galluso
Lionel Spinelli
Sophie Guia
Aurore Fenis
Eric Vivier
Eric Vivier
Eric Vivier
Yann M. Kerdiles
Type 1 Innate Lymphoid Cells Limit the Antitumoral Immune Response
description Natural killer (NK) cells are known to be able to kill established tumor cell lines, but important caveats remain regarding their roles in the detection and elimination of developing primary tumors. Using a genetic model of selective ILC1 and NK cell deficiency, we showed that these cells were dispensable for tumor immunosurveillance and immunoediting in the MCA-induced carcinogenesis model. However, we were able to generate primary cell lines derived from MCA-induced tumors with graded sensitivity to NK1.1+ cells (including NK cells and ILC1). This differential sensitivity was associated neither with a modulation of intratumoral NK cell frequency, nor the capacity of tumor cells to activate NK cells. Instead, ILC1 infiltration into the tumor was found to be a critical determinant of NK1.1+ cell-dependent tumor growth. Finally, bulk tumor RNAseq analysis identified a gene expression signature associated with tumor sensitivity to NK1.1+ cells. ILC1 therefore appear to play an active role in inhibiting the antitumoral immune response, prompting to evaluate the differential tumor infiltration of ILC1 and NK cells in patients to optimize the harnessing of immunity in cancer therapies.
format article
author Margaux Vienne
Marion Etiennot
Bertrand Escalière
Justine Galluso
Lionel Spinelli
Sophie Guia
Aurore Fenis
Eric Vivier
Eric Vivier
Eric Vivier
Yann M. Kerdiles
author_facet Margaux Vienne
Marion Etiennot
Bertrand Escalière
Justine Galluso
Lionel Spinelli
Sophie Guia
Aurore Fenis
Eric Vivier
Eric Vivier
Eric Vivier
Yann M. Kerdiles
author_sort Margaux Vienne
title Type 1 Innate Lymphoid Cells Limit the Antitumoral Immune Response
title_short Type 1 Innate Lymphoid Cells Limit the Antitumoral Immune Response
title_full Type 1 Innate Lymphoid Cells Limit the Antitumoral Immune Response
title_fullStr Type 1 Innate Lymphoid Cells Limit the Antitumoral Immune Response
title_full_unstemmed Type 1 Innate Lymphoid Cells Limit the Antitumoral Immune Response
title_sort type 1 innate lymphoid cells limit the antitumoral immune response
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/5d93b170ef1f4e6eba648775277a2912
work_keys_str_mv AT margauxvienne type1innatelymphoidcellslimittheantitumoralimmuneresponse
AT marionetiennot type1innatelymphoidcellslimittheantitumoralimmuneresponse
AT bertrandescaliere type1innatelymphoidcellslimittheantitumoralimmuneresponse
AT justinegalluso type1innatelymphoidcellslimittheantitumoralimmuneresponse
AT lionelspinelli type1innatelymphoidcellslimittheantitumoralimmuneresponse
AT sophieguia type1innatelymphoidcellslimittheantitumoralimmuneresponse
AT aurorefenis type1innatelymphoidcellslimittheantitumoralimmuneresponse
AT ericvivier type1innatelymphoidcellslimittheantitumoralimmuneresponse
AT ericvivier type1innatelymphoidcellslimittheantitumoralimmuneresponse
AT ericvivier type1innatelymphoidcellslimittheantitumoralimmuneresponse
AT yannmkerdiles type1innatelymphoidcellslimittheantitumoralimmuneresponse
_version_ 1718426605161807872