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Microbial peptides activate tumour-infiltrating lymphocytes in glioblastoma.
Naghavian, Reza; Faigle, Wolfgang; Oldrati, Pietro; Wang, Jian; Toussaint, Nora C; Qiu, Yuhan; Medici, Gioele; Wacker, Marcel; Freudenmann, Lena K; Bonté, Pierre-Emmanuel; Weller, Michael; Regli, Luca; Amigorena, Sebastian; Rammensee, Hans-Georg; Walz, Juliane S; Brugger, Silvio D; Mohme, Malte; Zhao, Yingdong; Sospedra, Mireia; Neidert, Marian C; Martin, Roland.
Afiliación
  • Naghavian R; Neuroimmunology and MS Research Section (NIMS), Neurology Clinic, University of Zurich, University Hospital Zurich, Zurich, Switzerland.
  • Faigle W; Cellerys AG, Schlieren, Switzerland.
  • Oldrati P; Neuroimmunology and MS Research Section (NIMS), Neurology Clinic, University of Zurich, University Hospital Zurich, Zurich, Switzerland.
  • Wang J; Cellerys AG, Schlieren, Switzerland.
  • Toussaint NC; Immunity and Cancer, Institut Curie, PSL University, INSERM U932, Paris, France.
  • Qiu Y; Neuroimmunology and MS Research Section (NIMS), Neurology Clinic, University of Zurich, University Hospital Zurich, Zurich, Switzerland.
  • Medici G; Neuroimmunology and MS Research Section (NIMS), Neurology Clinic, University of Zurich, University Hospital Zurich, Zurich, Switzerland.
  • Wacker M; School of Basic Medical Sciences, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
  • Freudenmann LK; NEXUS Personalized Health Technologies, ETH Zurich, Schlieren, Switzerland.
  • Bonté PE; Swiss Institute of Bioinformatics, Zurich, Switzerland.
  • Weller M; Neuroimmunology and MS Research Section (NIMS), Neurology Clinic, University of Zurich, University Hospital Zurich, Zurich, Switzerland.
  • Regli L; Clinical Neuroscience Center, Department of Neurosurgery, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
  • Amigorena S; Department of Peptide-based Immunotherapy, University of Tübingen, University Hospital Tübingen, Tübingen, Germany.
  • Rammensee HG; Institute for Cell Biology, Department of Immunology, University of Tübingen, Tübingen, Germany.
  • Walz JS; German Cancer Consortium (DKTK) and German Cancer Research Center (DKFZ), partner site Tübingen, Tübingen, Germany.
  • Brugger SD; Cluster of Excellence iFIT (EXC 2180) 'Image-Guided and Functionally Instructed Tumor Therapies', University of Tübingen, Tübingen, Germany.
  • Mohme M; Institute for Cell Biology, Department of Immunology, University of Tübingen, Tübingen, Germany.
  • Zhao Y; German Cancer Consortium (DKTK) and German Cancer Research Center (DKFZ), partner site Tübingen, Tübingen, Germany.
  • Sospedra M; Cluster of Excellence iFIT (EXC 2180) 'Image-Guided and Functionally Instructed Tumor Therapies', University of Tübingen, Tübingen, Germany.
  • Neidert MC; Immunity and Cancer, Institut Curie, PSL University, INSERM U932, Paris, France.
  • Martin R; Laboratory of Molecular Neuro-Oncology, Department of Neurology and Clinical Neuroscience, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Nature ; 617(7962): 807-817, 2023 05.
Article en En | MEDLINE | ID: mdl-37198490
ABSTRACT
Microbial organisms have key roles in numerous physiological processes in the human body and have recently been shown to modify the response to immune checkpoint inhibitors1,2. Here we aim to address the role of microbial organisms and their potential role in immune reactivity against glioblastoma. We demonstrate that HLA molecules of both glioblastoma tissues and tumour cell lines present bacteria-specific peptides. This finding prompted us to examine whether tumour-infiltrating lymphocytes (TILs) recognize tumour-derived bacterial peptides. Bacterial peptides eluted from HLA class II molecules are recognized by TILs, albeit very weakly. Using an unbiased antigen discovery approach to probe the specificity of a TIL CD4+ T cell clone, we show that it recognizes a broad spectrum of peptides from pathogenic bacteria, commensal gut microbiota and also glioblastoma-related tumour antigens. These peptides were also strongly stimulatory for bulk TILs and peripheral blood memory cells, which then respond to tumour-derived target peptides. Our data hint at how bacterial pathogens and bacterial gut microbiota can be involved in specific immune recognition of tumour antigens. The unbiased identification of microbial target antigens for TILs holds promise for future personalized tumour vaccination approaches.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fragmentos de Péptidos / Bacterias / Proteínas Bacterianas / Linfocitos Infiltrantes de Tumor / Glioblastoma / Antígenos de Neoplasias Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fragmentos de Péptidos / Bacterias / Proteínas Bacterianas / Linfocitos Infiltrantes de Tumor / Glioblastoma / Antígenos de Neoplasias Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article