ZNF683 marks a CD8

Hobit PD-1 Richter transformation ZNF683 checkpoint blockade chronic lymphocytic leukemia immunotherapy single-cell RNA sequencing t cells tox

Journal

Cancer cell
ISSN: 1878-3686
Titre abrégé: Cancer Cell
Pays: United States
ID NLM: 101130617

Informations de publication

Date de publication:
09 10 2023
Historique:
received: 14 07 2022
revised: 30 05 2023
accepted: 30 08 2023
pmc-release: 09 10 2024
medline: 3 11 2023
pubmed: 23 9 2023
entrez: 22 9 2023
Statut: ppublish

Résumé

Unlike many other hematologic malignancies, Richter syndrome (RS), an aggressive B cell lymphoma originating from indolent chronic lymphocytic leukemia, is responsive to PD-1 blockade. To discover the determinants of response, we analyze single-cell transcriptome data generated from 17 bone marrow samples longitudinally collected from 6 patients with RS. Response is associated with intermediate exhausted CD8 effector/effector memory T cells marked by high expression of the transcription factor ZNF683, determined to be evolving from stem-like memory cells and divergent from terminally exhausted cells. This signature overlaps with that of tumor-infiltrating populations from anti-PD-1 responsive solid tumors. ZNF683 is found to directly target key T cell genes (TCF7, LMO2, CD69) and impact pathways of T cell cytotoxicity and activation. Analysis of pre-treatment peripheral blood from 10 independent patients with RS treated with anti-PD-1, as well as patients with solid tumors treated with anti-PD-1, supports an association of ZNF683

Identifiants

pubmed: 37738974
pii: S1535-6108(23)00306-9
doi: 10.1016/j.ccell.2023.08.013
pmc: PMC10618915
mid: NIHMS1933974
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

1803-1816.e8

Subventions

Organisme : NCI NIH HHS
ID : P01 CA206978
Pays : United States
Organisme : NCI NIH HHS
ID : K08 CA270085
Pays : United States
Organisme : NCI NIH HHS
ID : R50 CA251956
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180861
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA155010
Pays : United States

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests C.J.W. receives funding support from: Pharmacyclics; holds equity in: BioNTech, Inc; G.G. is a founder, consultant and holds privately held equity in Scorpion Therapeutics, receives funding support from: IBM and Pharmacyclics, is an inventor on patent applications related to: MuTect, ABSOLUTE, MutSig, MSMuTect, MSMutSig, MSIDetect, POLYSOLVER, and TensorQTL; R.G. receives funding support from: Abbvie, Janssen, Gilead, AstraZeneca, and Roche; N.J. receives research funding from: Pharmacyclics, AbbVie, Genentech, AstraZeneca, BMS, Pfizer, Servier, ADC Therapeutics, Cellectis, Precision BioSciences, Adaptive Biotechnologies, Incyte, Aprea Therapeutics, Fate Therapeutics, Mingsight, Takeda, Medisix, Loxo Oncology, Novalgen and serves on Advisory Board/Honoraria: Pharmacyclics, Janssen, AbbVie, Genentech, AstraZeneca, BMS, Adaptive Biotechnologies, Precision BioSciences, Servier, Beigene, Cellectis, TG Therapeutics, ADC Therapeutics, MEI Pharma; W.G.W. reports funding from GSK/Novartis, Abbvie, Genentech, Pharmacyclics LLC, AstraZeneca/Acerta Pharma, Gilead Sciences, Juno Therapeutics, KITE Pharma, Sunesis, Miragen, Oncternal Therapeutics, Inc., Cyclacel, Loxo Oncology, Inc., Janssen, Xencor. B.A.K., C.J.W. and G.G. are inventors on patent: “Compositions, panels, and methods for characterizing chronic lymphocytic leukemia” (PCT/US21/45144); S.A.S. reports nonfinancial support from Bristol-Myers Squibb, and equity in Agenus Inc., Agios Pharmaceuticals, Breakbio Corp., Bristol-Myers Squibb and Lumos Pharma. N.P. is currently an employee of Bristol Myers Squibb. K.J.L. holds equity in Standard BioTools Inc. (formerly Fluidigm Corporation). C.J.W. and E.M.P are inventors on a patent, US Utility Application No. US-2022-0298580-A1 filed on 02/10/2022, International Application No. WO/2021/041669 filed on 9/15/2022, “Immune Signatures Predictive of Response to PD-1 Blockade in Richter’s transformation.” M.D., J.D.K. and B.T. have no relevant conflict of interest. C.T. reports honorarium from Beigene, Janssen, Abbvie, AZ and LOXO and research funding from Beigene, Janssen, and AbbVie.

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Auteurs

Erin M Parry (EM)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Harvard Medical School, Boston, MA 02115, USA; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.

Camilla K Lemvigh (CK)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Department of Health Technology, Technical University of Denmark, 2800 Kongens Lyngby, Denmark.

Stephanie Deng (S)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.

Nathan Dangle (N)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.

Neil Ruthen (N)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.

Binyamin A Knisbacher (BA)

Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.

Julien Broséus (J)

Inserm UMRS1256 Nutrition-Génétique et Exposition Aux Risques Environnementaux (N-GERE), Université de Lorraine, 54000 Nancy, France; Université de Lorraine, CHRU-Nancy, Service d'hématologie Biologique, Pôle Laboratoires, 54000 Nancy, France.

Sébastien Hergalant (S)

Inserm UMRS1256 Nutrition-Génétique et Exposition Aux Risques Environnementaux (N-GERE), Université de Lorraine, 54000 Nancy, France.

Romain Guièze (R)

CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France; EA 7453 (CHELTER), Université Clermont Auvergne, 63001 Clermont-Ferrand, France.

Shuqiang Li (S)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA; Translational Immunogenomics Lab, Dana-Farber Cancer Institute, Boston, MA 02215, USA.

Wandi Zhang (W)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.

Connor Johnson (C)

Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.

Jaclyn M Long (JM)

Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA; Department of Immunology, Blavatnik Institute, Harvard Medical School, Boston, MA 02115, USA; Evergrande Center for Immunologic Diseases, Harvard Medical School and Brigham and Women's Hospital, Boston, MA 02115, USA; Division of Gastroenterology, Hepatology, and Nutrition, Boston Children's Hospital, Boston, MA 02115, USA.

Shanye Yin (S)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.

Lillian Werner (L)

Department of Data Science, Dana-Farber Cancer Institute, Boston, MA 02215, USA.

Annabelle Anandappa (A)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.

Noelia Purroy (N)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.

Satyen Gohil (S)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.

Giacomo Oliveira (G)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Harvard Medical School, Boston, MA 02115, USA.

Pavan Bachireddy (P)

Department of Hematopoietic Biology and Malignancy, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

Sachet A Shukla (SA)

Department of Hematopoietic Biology and Malignancy, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

Teddy Huang (T)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Translational Immunogenomics Lab, Dana-Farber Cancer Institute, Boston, MA 02215, USA.

Joseph D Khoury (JD)

Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, USA.

Beenu Thakral (B)

Department of Hematopathology, University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.

Michael Dickinson (M)

Peter MacCallum Cancer Centre, Royal Melbourne Hospital, Melbourne, VIC, Australia; Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, VIC, Australia.

Constantine Tam (C)

Alfred Health, Melbourne, VIC, Australia; Monash University, Melbourne, VIC, Australia.

Kenneth J Livak (KJ)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Translational Immunogenomics Lab, Dana-Farber Cancer Institute, Boston, MA 02215, USA.

Gad Getz (G)

Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.

Donna Neuberg (D)

Department of Data Science, Dana-Farber Cancer Institute, Boston, MA 02215, USA.

Pierre Feugier (P)

Inserm UMRS1256 Nutrition-Génétique et Exposition Aux Risques Environnementaux (N-GERE), Université de Lorraine, 54000 Nancy, France; Université de Lorraine, CHRU Nancy, service d'hématologie clinique, Nancy, France.

Peter Kharchenko (P)

Department of Biomedical Informatics, Harvard Medical School, Boston, MA 02215, USA.

William Wierda (W)

Department of Leukemia, University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.

Lars Rønn Olsen (LR)

Department of Health Technology, Technical University of Denmark, 2800 Kongens Lyngby, Denmark.

Nitin Jain (N)

Department of Leukemia, University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.

Catherine J Wu (CJ)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Harvard Medical School, Boston, MA 02115, USA; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA. Electronic address: Catherine_wu@dfci.harvard.edu.

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