Agonistic CD40 therapy induces tertiary lymphoid structures but impairs responses to checkpoint blockade in glioma

Agonistic CD40 antibodies (αCD40) have broad immunostimulatory properties, however their efficacy in glioma remains unclear. Here the authors show that αCD40 promotes the formation of tertiary lymphoid structures but does not improve survival and impairs the response to immune checkpoint blockade in...

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Main Authors: Luuk van Hooren, Alessandra Vaccaro, Mohanraj Ramachandran, Konstantinos Vazaios, Sylwia Libard, Tiarne van de Walle, Maria Georganaki, Hua Huang, Ilkka Pietilä, Joey Lau, Maria H. Ulvmar, Mikael C. I. Karlsson, Maria Zetterling, Sara M. Mangsbo, Asgeir S. Jakola, Thomas Olsson Bontell, Anja Smits, Magnus Essand, Anna Dimberg
Format: Article
Language:English
Published: Nature Publishing Group 2021-07-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-021-24347-7
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spelling doaj-960c23767579410eb75556847b8c9b3f2021-07-11T11:42:49ZengNature Publishing GroupNature Communications2041-17232021-07-0112111410.1038/s41467-021-24347-7Agonistic CD40 therapy induces tertiary lymphoid structures but impairs responses to checkpoint blockade in gliomaLuuk van Hooren0Alessandra Vaccaro1Mohanraj Ramachandran2Konstantinos Vazaios3Sylwia Libard4Tiarne van de Walle5Maria Georganaki6Hua Huang7Ilkka Pietilä8Joey Lau9Maria H. Ulvmar10Mikael C. I. Karlsson11Maria Zetterling12Sara M. Mangsbo13Asgeir S. Jakola14Thomas Olsson Bontell15Anja Smits16Magnus Essand17Anna Dimberg18Department of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala UniversityDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala UniversityDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala UniversityDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala UniversityDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala UniversityDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala UniversityDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala UniversityDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala UniversityDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala UniversityDepartment of Medical Cell Biology, Uppsala UniversityDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala UniversityDepartment of Microbiology, Tumor and Cell Biology, Karolinska InstitutetDepartment of Neuroscience, Neurology, Uppsala UniversityDepartment of Pharmaceutical Biosciences, Science for Life Laboratory, Uppsala UniversityDepartment of Neurosurgery, Sahlgrenska University HospitalDepartment of Physiology, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of GothenburgDepartment of Neuroscience, Neurology, Uppsala UniversityDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala UniversityDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala UniversityAgonistic CD40 antibodies (αCD40) have broad immunostimulatory properties, however their efficacy in glioma remains unclear. Here the authors show that αCD40 promotes the formation of tertiary lymphoid structures but does not improve survival and impairs the response to immune checkpoint blockade in murine glioma models.https://doi.org/10.1038/s41467-021-24347-7
collection DOAJ
language English
format Article
sources DOAJ
author Luuk van Hooren
Alessandra Vaccaro
Mohanraj Ramachandran
Konstantinos Vazaios
Sylwia Libard
Tiarne van de Walle
Maria Georganaki
Hua Huang
Ilkka Pietilä
Joey Lau
Maria H. Ulvmar
Mikael C. I. Karlsson
Maria Zetterling
Sara M. Mangsbo
Asgeir S. Jakola
Thomas Olsson Bontell
Anja Smits
Magnus Essand
Anna Dimberg
spellingShingle Luuk van Hooren
Alessandra Vaccaro
Mohanraj Ramachandran
Konstantinos Vazaios
Sylwia Libard
Tiarne van de Walle
Maria Georganaki
Hua Huang
Ilkka Pietilä
Joey Lau
Maria H. Ulvmar
Mikael C. I. Karlsson
Maria Zetterling
Sara M. Mangsbo
Asgeir S. Jakola
Thomas Olsson Bontell
Anja Smits
Magnus Essand
Anna Dimberg
Agonistic CD40 therapy induces tertiary lymphoid structures but impairs responses to checkpoint blockade in glioma
Nature Communications
author_facet Luuk van Hooren
Alessandra Vaccaro
Mohanraj Ramachandran
Konstantinos Vazaios
Sylwia Libard
Tiarne van de Walle
Maria Georganaki
Hua Huang
Ilkka Pietilä
Joey Lau
Maria H. Ulvmar
Mikael C. I. Karlsson
Maria Zetterling
Sara M. Mangsbo
Asgeir S. Jakola
Thomas Olsson Bontell
Anja Smits
Magnus Essand
Anna Dimberg
author_sort Luuk van Hooren
title Agonistic CD40 therapy induces tertiary lymphoid structures but impairs responses to checkpoint blockade in glioma
title_short Agonistic CD40 therapy induces tertiary lymphoid structures but impairs responses to checkpoint blockade in glioma
title_full Agonistic CD40 therapy induces tertiary lymphoid structures but impairs responses to checkpoint blockade in glioma
title_fullStr Agonistic CD40 therapy induces tertiary lymphoid structures but impairs responses to checkpoint blockade in glioma
title_full_unstemmed Agonistic CD40 therapy induces tertiary lymphoid structures but impairs responses to checkpoint blockade in glioma
title_sort agonistic cd40 therapy induces tertiary lymphoid structures but impairs responses to checkpoint blockade in glioma
publisher Nature Publishing Group
series Nature Communications
issn 2041-1723
publishDate 2021-07-01
description Agonistic CD40 antibodies (αCD40) have broad immunostimulatory properties, however their efficacy in glioma remains unclear. Here the authors show that αCD40 promotes the formation of tertiary lymphoid structures but does not improve survival and impairs the response to immune checkpoint blockade in murine glioma models.
url https://doi.org/10.1038/s41467-021-24347-7
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