دورية أكاديمية

BTN2A1, an immune checkpoint targeting Vγ9Vδ2 T cell cytotoxicity against malignant cells

التفاصيل البيبلوغرافية
العنوان: BTN2A1, an immune checkpoint targeting Vγ9Vδ2 T cell cytotoxicity against malignant cells
المؤلفون: Cano, Carla, Pasero, Christine, de Gassart, Aude, Kerneur, Clement, Gabriac, Mélanie, Fullana, Marie, Granarolo, Emilie, Hoet, René, Scotet, Emmanuel, Rafia, Chirine, Herrmann, Thomas, Imbert, Caroline, Gorvel, Laurent, Vey, Norbert, Briantais, Antoine, Le Floch, Anne Charlotte, Olive, Daniel
المساهمون: ImCheck Therapeutics Marseille, Immunobiology of Human αβ and γδ T Cells and Immunotherapeutic Applications (CRCINA-ÉQUIPE 1), Centre de Recherche en Cancérologie et Immunologie Nantes-Angers (CRCINA), Université d'Angers (UA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Centre Hospitalier Universitaire de Nantes = Nantes University Hospital (CHU Nantes)-Université de Nantes - UFR de Médecine et des Techniques Médicales (UFR MEDECINE), Université de Nantes (UN)-Université de Nantes (UN)-Université d'Angers (UA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Centre Hospitalier Universitaire de Nantes = Nantes University Hospital (CHU Nantes)-Université de Nantes - UFR de Médecine et des Techniques Médicales (UFR MEDECINE), Université de Nantes (UN)-Université de Nantes (UN), LabEX IGO Immunothérapie Grand Ouest, Nantes Université (Nantes Univ), Julius-Maximilians-Universität Würzburg (JMU), Centre de Recherche en Cancérologie de Marseille (CRCM), Aix Marseille Université (AMU)-Institut Paoli-Calmettes (IPC), Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Institut Paoli-Calmettes (IPC), Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)
المصدر: ISSN: 2211-1247.
بيانات النشر: HAL CCSD
Elsevier Inc
سنة النشر: 2021
المجموعة: Université de Nantes: HAL-UNIV-NANTES
مصطلحات موضوعية: BTN2A1, BTN3A, Vγ9Vδ2 T cells, butyrophilins, cancer, immunotherapy, monoclonal antibodies, [SDV.CAN]Life Sciences [q-bio]/Cancer
الوصف: International audience ; The anti-tumor response of Vγ9Vδ2 T cells requires the sensing of accumulated phosphoantigens (pAgs) bound intracellularly to butyrophilin 3A1 (BTN3A1). In this study, we show that butyrophilin 2A1 (BTN2A1) is required for BTN3A-mediated Vγ9Vδ2 T cell cytotoxicity against cancer cells, and that expression of the BTN2A1/BTN3A1 complex is sufficient to trigger Vγ9Vδ2 TCR activation. Also, BTN2A1 interacts with all isoforms of BTN3A (BTN3A1, BTN3A2, BTN3A3), which appears to be a rate-limiting factor to BTN2A1 export to the plasma membrane. BTN2A1/BTN3A1 interaction is enhanced by pAgs and, strikingly, B30.2 domains of both proteins are required for pAg responsiveness. BTN2A1 expression in cancer cells correlates with bisphosphonate-induced Vγ9Vδ2 T cell cytotoxicity. Vγ9Vδ2 T cell killing of cancer cells is modulated by anti-BTN2A1 monoclonal antibodies (mAbs), whose action relies on the inhibition of BTN2A1 binding to the Vγ9Vδ2TCR. This demonstrates the potential of BTN2A1 as a therapeutic target and adds to the emerging butyrophilin-family cooperation pathway in γδ T cell activation.
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34260935; inserm-03547155; https://inserm.hal.science/inserm-03547155Test; https://inserm.hal.science/inserm-03547155/documentTest; https://inserm.hal.science/inserm-03547155/file/PIIS2211124721007579.pdfTest; PUBMED: 34260935
DOI: 10.1016/j.celrep.2021.109359
الإتاحة: https://doi.org/10.1016/j.celrep.2021.109359Test
https://inserm.hal.science/inserm-03547155Test
https://inserm.hal.science/inserm-03547155/documentTest
https://inserm.hal.science/inserm-03547155/file/PIIS2211124721007579.pdfTest
حقوق: info:eu-repo/semantics/OpenAccess
رقم الانضمام: edsbas.CE0C24B
قاعدة البيانات: BASE