Tumor invasion in draining lymph nodes is associated with Treg accumulation in breast cancer patients.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
29 06 2020
Historique:
received: 24 01 2020
accepted: 04 06 2020
entrez: 1 7 2020
pubmed: 1 7 2020
medline: 29 8 2020
Statut: epublish

Résumé

Tumor-draining lymph node (TDLN) invasion by metastatic cells in breast cancer correlates with poor prognosis and is associated with local immunosuppression, which can be partly mediated by regulatory T cells (Tregs). Here, we study Tregs from matched tumor-invaded and non-invaded TDLNs, and breast tumors. We observe that Treg frequencies increase with nodal invasion, and that Tregs express higher levels of co-inhibitory/stimulatory receptors than effector cells. Also, while Tregs show conserved suppressive function in TDLN and tumor, conventional T cells (Tconvs) in TDLNs proliferate and produce Th1-inflammatory cytokines, but are dysfunctional in the tumor. We describe a common transcriptomic signature shared by Tregs from tumors and nodes, including CD80, which is significantly associated with poor patient survival. TCR RNA-sequencing analysis indicates trafficking between TDLNs and tumors and ongoing Tconv/Treg conversion. Overall, TDLN Tregs are functional and express a distinct pattern of druggable co-receptors, highlighting their potential as targets for cancer immunotherapy.

Identifiants

pubmed: 32601304
doi: 10.1038/s41467-020-17046-2
pii: 10.1038/s41467-020-17046-2
pmc: PMC7324591
doi:

Substances chimiques

B7-1 Antigen 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3272

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Auteurs

Nicolas Gonzalo Núñez (NG)

Institut Curie, PSL Research University, INSERM U932, F-75005, Paris, France.
Institute of Experimental Immunology, University of Zurich, Winterthurerstr. 190, CH-8057, Zurich, Switzerland.

Jimena Tosello Boari (J)

Institut Curie, PSL Research University, INSERM U932, F-75005, Paris, France.

Rodrigo Nalio Ramos (RN)

Institut Curie, PSL Research University, INSERM U932, F-75005, Paris, France.

Wilfrid Richer (W)

Institut Curie, PSL Research University, INSERM U932, F-75005, Paris, France.

Nicolas Cagnard (N)

Paris-Descartes Bioinformatics Platform, 75015, Paris, France.

Cyrill Dimitri Anderfuhren (CD)

Institute of Experimental Immunology, University of Zurich, Winterthurerstr. 190, CH-8057, Zurich, Switzerland.

Leticia Laura Niborski (LL)

Institut Curie, PSL Research University, INSERM U932, F-75005, Paris, France.

Jeremy Bigot (J)

Institut Curie, PSL Research University, INSERM U932, F-75005, Paris, France.

Didier Meseure (D)

Institut Curie, PSL Research University, Departement de Biologie des Tumeurs, F-75005, Paris, France.
Centre d'Investigation Clinique Biotherapie CICBT 1428, Institut Curie, Paris, F-75005, France.

Philippe De La Rochere (P)

Institut Curie, PSL Research University, INSERM U932, F-75005, Paris, France.

Maud Milder (M)

Institut Curie, PSL Research University, Departement de Biologie des Tumeurs, F-75005, Paris, France.
Centre d'Investigation Clinique Biotherapie CICBT 1428, Institut Curie, Paris, F-75005, France.

Sophie Viel (S)

Institut Curie, PSL Research University, INSERM U932, F-75005, Paris, France.

Delphine Loirat (D)

Institut Curie, PSL Research University, INSERM U932, F-75005, Paris, France.
Centre d'Investigation Clinique Biotherapie CICBT 1428, Institut Curie, Paris, F-75005, France.
Institut Curie, PSL Research University, Departement d'Oncologie Medicale, F-75005, Paris, France.

Louis Pérol (L)

Institut Curie, PSL Research University, INSERM U932, F-75005, Paris, France.

Anne Vincent-Salomon (A)

Institut Curie, PSL Research University, Departement de Biologie des Tumeurs, F-75005, Paris, France.
Centre d'Investigation Clinique Biotherapie CICBT 1428, Institut Curie, Paris, F-75005, France.

Xavier Sastre-Garau (X)

Institut Curie, PSL Research University, Departement de Biologie des Tumeurs, F-75005, Paris, France.
Institut de Cancerologie de Lorraine Department of Biopathology, 6, avenue de Bourgogne CS 30519, 54519, Vandoeuvre-lès-Nancy cedex, France.

Becher Burkhard (B)

Institute of Experimental Immunology, University of Zurich, Winterthurerstr. 190, CH-8057, Zurich, Switzerland.

Christine Sedlik (C)

Institut Curie, PSL Research University, INSERM U932, F-75005, Paris, France.
Centre d'Investigation Clinique Biotherapie CICBT 1428, Institut Curie, Paris, F-75005, France.

Olivier Lantz (O)

Institut Curie, PSL Research University, INSERM U932, F-75005, Paris, France.
Institut Curie, PSL Research University, Departement de Biologie des Tumeurs, F-75005, Paris, France.
Centre d'Investigation Clinique Biotherapie CICBT 1428, Institut Curie, Paris, F-75005, France.

Sebastian Amigorena (S)

Institut Curie, PSL Research University, INSERM U932, F-75005, Paris, France.
Centre d'Investigation Clinique Biotherapie CICBT 1428, Institut Curie, Paris, F-75005, France.

Eliane Piaggio (E)

Institut Curie, PSL Research University, INSERM U932, F-75005, Paris, France. eliane.piaggio@curie.fr.
Centre d'Investigation Clinique Biotherapie CICBT 1428, Institut Curie, Paris, F-75005, France. eliane.piaggio@curie.fr.

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