ILC2-modulated T cell-to-MDSC balance is associated with bladder cancer recurrence
Non-muscle-invasive bladder cancer (NMIBC) is a highly recurrent tumor despite intravesical immunotherapy instillation with the bacillus Calmette-Guérin (BCG) vaccine. In a prospective longitudinal study, we took advantage of BCG instillations, which increase local immune infiltration, to characteri...
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Published in: | The Journal of clinical investigation Vol. 127; no. 8; pp. 2916 - 2929 |
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Main Authors: | , , , , , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
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American Society for Clinical Investigation
01-08-2017
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Abstract | Non-muscle-invasive bladder cancer (NMIBC) is a highly recurrent tumor despite intravesical immunotherapy instillation with the bacillus Calmette-Guérin (BCG) vaccine. In a prospective longitudinal study, we took advantage of BCG instillations, which increase local immune infiltration, to characterize immune cell populations in the urine of patients with NMIBC as a surrogate for the bladder tumor microenvironment. We observed an infiltration of neutrophils, T cells, monocytic myeloid-derived suppressor cells (M-MDSCs), and group 2 innate lymphoid cells (ILC2). Notably, patients with a T cell-to-MDSC ratio of less than 1 showed dramatically lower recurrence-free survival than did patients with a ratio of greater than 1. Analysis of early and later time points indicated that this patient dichotomy existed prior to BCG treatment. ILC2 frequency was associated with detectable IL-13 in the urine and correlated with the level of recruited M-MDSCs, which highly expressed IL-13 receptor α1. In vitro, ILC2 were increased and potently expressed IL-13 in the presence of BCG or tumor cells. IL-13 induced the preferential recruitment and suppressive function of monocytes. Thus, the T cell-to-MDSC balance, associated with a skewing toward type 2 immunity, may predict bladder tumor recurrence and influence the mortality of patients with muscle-invasive cancer. Moreover, these results underline the ILC2/IL-13 axis as a targetable pathway to curtail the M-MDSC compartment and improve bladder cancer treatment. |
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AbstractList | Non-muscle-invasive bladder cancer (NMIBC) is a highly recurrent tumor despite intravesical immunotherapy instillation with the bacillus Calmette-Guerin (BCG) vaccine. In a prospective longitudinal study, we took advantage of BCG instillations, which increase local immune infiltration, to characterize immune cell populations in the urine of patients with NMIBC as a surrogate for the bladder tumor microenvironment. We observed an infiltration of neutrophils, T cells, monocytic myeloidderived suppressor cells (M-MDSCs), and group 2 innate lymphoid cells (ILC2). Notably, patients with a T cell-to-MDSC ratio of less than 1 showed dramatically lower recurrence-free survival than did patients with a ratio of greater than 1. Analysis of early and later time points indicated that this patient dichotomy existed prior to BCG treatment. ILC2 frequency was associated with detectable IL-13 in the urine and correlated with the level of recruited M-MDSCs, which highly expressed IL-13 receptor [alpha]1. In vitro, ILC2 were increased and potently expressed IL-13 in the presence of BCG or tumor cells. IL-13 induced the preferential recruitment and suppressive function of monocytes. Thus, the T cell-to-MDSC balance, associated with a skewing toward type 2 immunity, may predict bladder tumor recurrence and influence the mortality of patients with muscle-invasive cancer. Moreover, these results underline the ILC2/IL-13 axis as a targetable pathway to curtail the M-MDSC compartment and improve bladder cancer treatment. Non-muscle–invasive bladder cancer (NMIBC) is a highly recurrent tumor despite intravesical immunotherapy instillation with the bacillus Calmette-Guérin (BCG) vaccine. In a prospective longitudinal study, we took advantage of BCG instillations, which increase local immune infiltration, to characterize immune cell populations in the urine of patients with NMIBC as a surrogate for the bladder tumor microenvironment. We observed an infiltration of neutrophils, T cells, monocytic myeloid-derived suppressor cells (M-MDSCs), and group 2 innate lymphoid cells (ILC2). Notably, patients with a T cell–to-MDSC ratio of less than 1 showed dramatically lower recurrence-free survival than did patients with a ratio of greater than 1. Analysis of early and later time points indicated that this patient dichotomy existed prior to BCG treatment. ILC2 frequency was associated with detectable IL-13 in the urine and correlated with the level of recruited M-MDSCs, which highly expressed IL-13 receptor α1. In vitro, ILC2 were increased and potently expressed IL-13 in the presence of BCG or tumor cells. IL-13 induced the preferential recruitment and suppressive function of monocytes. Thus, the T cell–to-MDSC balance, associated with a skewing toward type 2 immunity, may predict bladder tumor recurrence and influence the mortality of patients with muscle-invasive cancer. Moreover, these results underline the ILC2/IL-13 axis as a targetable pathway to curtail the M-MDSC compartment and improve bladder cancer treatment. |
Audience | Academic |
Author | Chevalier, Mathieu F Cesson, Valérie Rentsch, Cyrill A Jandus, Camilla Salomé, Bérengère Domingos-Pereira, Sonia Gfeller, David Derré, Laurent Fritschi, Anne-Sophie Racle, Julien Speiser, Daniel E Dartiguenave, Florence Nardelli-Haefliger, Denise Trabanelli, Sara Gharbi, Dalila Bohner, Perrine Jichlinski, Patrice |
AuthorAffiliation | 3 Computational Cancer Biology, Ludwig Center for Cancer Research at the University of Lausanne, Epalinges, Switzerland 5 Department of Oncology and Ludwig Center for Cancer Research, University of Lausanne, Epalinges, Switzerland 4 Swiss Institute of Bioinformatics (SIB), Lausanne, Switzerland 2 Translational Tumor Immunology, Ludwig Center for Cancer Research at the University of Lausanne, Department of Fundamental Oncology, Epalinges, Switzerland 1 Urology Research Unit, University Hospital of Lausanne (CHUV), Lausanne, Switzerland 6 Department of Urology, University Hospital of Basel, Basel, Switzerland |
AuthorAffiliation_xml | – name: 3 Computational Cancer Biology, Ludwig Center for Cancer Research at the University of Lausanne, Epalinges, Switzerland – name: 2 Translational Tumor Immunology, Ludwig Center for Cancer Research at the University of Lausanne, Department of Fundamental Oncology, Epalinges, Switzerland – name: 4 Swiss Institute of Bioinformatics (SIB), Lausanne, Switzerland – name: 6 Department of Urology, University Hospital of Basel, Basel, Switzerland – name: 1 Urology Research Unit, University Hospital of Lausanne (CHUV), Lausanne, Switzerland – name: 5 Department of Oncology and Ludwig Center for Cancer Research, University of Lausanne, Epalinges, Switzerland |
Author_xml | – sequence: 1 givenname: Mathieu F surname: Chevalier fullname: Chevalier, Mathieu F organization: Urology Research Unit, University Hospital of Lausanne (CHUV), Lausanne, Switzerland – sequence: 2 givenname: Sara surname: Trabanelli fullname: Trabanelli, Sara organization: Translational Tumor Immunology, Ludwig Center for Cancer Research at the University of Lausanne, Department of Fundamental Oncology, Epalinges, Switzerland – sequence: 3 givenname: Julien surname: Racle fullname: Racle, Julien organization: Swiss Institute of Bioinformatics (SIB), Lausanne, Switzerland – sequence: 4 givenname: Bérengère surname: Salomé fullname: Salomé, Bérengère organization: Translational Tumor Immunology, Ludwig Center for Cancer Research at the University of Lausanne, Department of Fundamental Oncology, Epalinges, Switzerland – sequence: 5 givenname: Valérie surname: Cesson fullname: Cesson, Valérie organization: Urology Research Unit, University Hospital of Lausanne (CHUV), Lausanne, Switzerland – sequence: 6 givenname: Dalila surname: Gharbi fullname: Gharbi, Dalila organization: Urology Research Unit, University Hospital of Lausanne (CHUV), Lausanne, Switzerland – sequence: 7 givenname: Perrine surname: Bohner fullname: Bohner, Perrine organization: Urology Research Unit, University Hospital of Lausanne (CHUV), Lausanne, Switzerland – sequence: 8 givenname: Sonia surname: Domingos-Pereira fullname: Domingos-Pereira, Sonia organization: Urology Research Unit, University Hospital of Lausanne (CHUV), Lausanne, Switzerland – sequence: 9 givenname: Florence surname: Dartiguenave fullname: Dartiguenave, Florence organization: Urology Research Unit, University Hospital of Lausanne (CHUV), Lausanne, Switzerland – sequence: 10 givenname: Anne-Sophie surname: Fritschi fullname: Fritschi, Anne-Sophie organization: Urology Research Unit, University Hospital of Lausanne (CHUV), Lausanne, Switzerland – sequence: 11 givenname: Daniel E surname: Speiser fullname: Speiser, Daniel E organization: Department of Oncology and Ludwig Center for Cancer Research, University of Lausanne, Epalinges, Switzerland – sequence: 12 givenname: Cyrill A surname: Rentsch fullname: Rentsch, Cyrill A organization: Department of Urology, University Hospital of Basel, Basel, Switzerland – sequence: 13 givenname: David surname: Gfeller fullname: Gfeller, David organization: Swiss Institute of Bioinformatics (SIB), Lausanne, Switzerland – sequence: 14 givenname: Patrice surname: Jichlinski fullname: Jichlinski, Patrice organization: Urology Research Unit, University Hospital of Lausanne (CHUV), Lausanne, Switzerland – sequence: 15 givenname: Denise surname: Nardelli-Haefliger fullname: Nardelli-Haefliger, Denise organization: Urology Research Unit, University Hospital of Lausanne (CHUV), Lausanne, Switzerland – sequence: 16 givenname: Camilla surname: Jandus fullname: Jandus, Camilla organization: Translational Tumor Immunology, Ludwig Center for Cancer Research at the University of Lausanne, Department of Fundamental Oncology, Epalinges, Switzerland – sequence: 17 givenname: Laurent surname: Derré fullname: Derré, Laurent organization: Urology Research Unit, University Hospital of Lausanne (CHUV), Lausanne, Switzerland |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28650339$$D View this record in MEDLINE/PubMed |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Authorship note: M.F. Chevalier and S. Trabanelli contributed equally to this work. L. Derré and C. Jandus equally contributed to this work as co–senior authors. |
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SubjectTerms | Administration, Intravesical Aged Aged, 80 and over Analysis Antigens Bacillus Calmette-Guerin vaccine BCG BCG Vaccine Biomedical research Bladder cancer Cancer Cellular signal transduction Disease-Free Survival Female Gene expression Genotype & phenotype Humans Immune System Immunotherapy Interleukin 13 Interleukin-13 - metabolism Invasiveness Leprosy Leukocytes (neutrophilic) Longitudinal Studies Lymphocytes Lymphocytes - cytology Lymphocytes T Lymphoid cells Male Metastases Middle Aged Monocytes Monocytes - cytology Neoplasm Recurrence, Local - immunology Neoplasm Recurrence, Local - urine Neutrophils Neutrophils - cytology Patients Prospective Studies Recurrence (Disease) Rodents Suppressor cells Survival analysis T cells T-Lymphocytes - cytology Tumor cells Urinary bladder Urinary Bladder Neoplasms - immunology Urinary Bladder Neoplasms - therapy Urinary Bladder Neoplasms - urine Urine |
Title | ILC2-modulated T cell-to-MDSC balance is associated with bladder cancer recurrence |
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