Author
Listed:
- Reza Naghavian
(University of Zurich, University Hospital Zurich
Cellerys AG)
- Wolfgang Faigle
(University of Zurich, University Hospital Zurich
Cellerys AG
PSL University, INSERM U932)
- Pietro Oldrati
(University of Zurich, University Hospital Zurich)
- Jian Wang
(University of Zurich, University Hospital Zurich
University of Science and Technology of China)
- Nora C. Toussaint
(ETH Zurich
Swiss Institute of Bioinformatics)
- Yuhan Qiu
(University of Zurich, University Hospital Zurich)
- Gioele Medici
(University Hospital Zurich, University of Zurich)
- Marcel Wacker
(University of Tübingen, University Hospital Tübingen
University of Tübingen
German Cancer Consortium (DKTK) and German Cancer Research Center (DKFZ), partner site Tübingen
University of Tübingen)
- Lena K. Freudenmann
(University of Tübingen
German Cancer Consortium (DKTK) and German Cancer Research Center (DKFZ), partner site Tübingen
University of Tübingen)
- Pierre-Emmanuel Bonté
(PSL University, INSERM U932)
- Michael Weller
(University Hospital Zurich, University of Zurich)
- Luca Regli
(University Hospital Zurich, University of Zurich)
- Sebastian Amigorena
(PSL University, INSERM U932)
- Hans-Georg Rammensee
(University of Tübingen
German Cancer Consortium (DKTK) and German Cancer Research Center (DKFZ), partner site Tübingen
University of Tübingen)
- Juliane S. Walz
(University of Tübingen, University Hospital Tübingen
University of Tübingen
German Cancer Consortium (DKTK) and German Cancer Research Center (DKFZ), partner site Tübingen
University of Tübingen)
- Silvio D. Brugger
(University Hospital Zurich, University of Zurich)
- Malte Mohme
(University Hospital Hamburg Eppendorf, University of Hamburg)
- Yingdong Zhao
(Computational and Systems Biology Branch, Biometric Research Program, Division of Cancer Treatment and Diagnosis, NCI, NIH)
- Mireia Sospedra
(University of Zurich, University Hospital Zurich
Cellerys AG)
- Marian C. Neidert
(University Hospital Zurich, University of Zurich
Cantonal Hospital St. Gallen)
- Roland Martin
(University of Zurich, University Hospital Zurich
Cellerys AG
University of Zurich
Karolinska Institutet)
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.
Suggested Citation
Reza Naghavian & Wolfgang Faigle & Pietro Oldrati & Jian Wang & Nora C. Toussaint & Yuhan Qiu & Gioele Medici & Marcel Wacker & Lena K. Freudenmann & Pierre-Emmanuel Bonté & Michael Weller & Luca Regl, 2023.
"Microbial peptides activate tumour-infiltrating lymphocytes in glioblastoma,"
Nature, Nature, vol. 617(7962), pages 807-817, May.
Handle:
RePEc:nat:nature:v:617:y:2023:i:7962:d:10.1038_s41586-023-06081-w
DOI: 10.1038/s41586-023-06081-w
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