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LAG-3 expression in the inflammatory microenvironment of glioma
by
Preusser Matthias
, Dieckmann, Karin
, Feldmann Katharina
, Widhalm Georg
, Wöhrer Adelheid
, Kiesel, Barbara
, Müllauer Leonhard
, Mair, Maximilian J
, Berghoff, Anna S
in
Biobanks
/ Brain cancer
/ CD20 antigen
/ CD223 antigen
/ CD3 antigen
/ CD8 antigen
/ Cell activation
/ Clinical trials
/ DNA methylation
/ DNA methyltransferase
/ Glioblastoma
/ Glioma
/ Immune checkpoint inhibitors
/ Immunohistochemistry
/ Immunotherapy
/ Inflammation
/ Lymphocytes
/ Metastases
/ Methylguanine
/ Microenvironments
/ O6-methylguanine-DNA methyltransferase
/ Oncology
/ Patients
/ PD-1 protein
/ PD-L1 protein
/ Response rates
/ Statistical analysis
/ Tumor cells
/ Tumor-infiltrating lymphocytes
/ Tumors
2021
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LAG-3 expression in the inflammatory microenvironment of glioma
by
Preusser Matthias
, Dieckmann, Karin
, Feldmann Katharina
, Widhalm Georg
, Wöhrer Adelheid
, Kiesel, Barbara
, Müllauer Leonhard
, Mair, Maximilian J
, Berghoff, Anna S
in
Biobanks
/ Brain cancer
/ CD20 antigen
/ CD223 antigen
/ CD3 antigen
/ CD8 antigen
/ Cell activation
/ Clinical trials
/ DNA methylation
/ DNA methyltransferase
/ Glioblastoma
/ Glioma
/ Immune checkpoint inhibitors
/ Immunohistochemistry
/ Immunotherapy
/ Inflammation
/ Lymphocytes
/ Metastases
/ Methylguanine
/ Microenvironments
/ O6-methylguanine-DNA methyltransferase
/ Oncology
/ Patients
/ PD-1 protein
/ PD-L1 protein
/ Response rates
/ Statistical analysis
/ Tumor cells
/ Tumor-infiltrating lymphocytes
/ Tumors
2021
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LAG-3 expression in the inflammatory microenvironment of glioma
by
Preusser Matthias
, Dieckmann, Karin
, Feldmann Katharina
, Widhalm Georg
, Wöhrer Adelheid
, Kiesel, Barbara
, Müllauer Leonhard
, Mair, Maximilian J
, Berghoff, Anna S
in
Biobanks
/ Brain cancer
/ CD20 antigen
/ CD223 antigen
/ CD3 antigen
/ CD8 antigen
/ Cell activation
/ Clinical trials
/ DNA methylation
/ DNA methyltransferase
/ Glioblastoma
/ Glioma
/ Immune checkpoint inhibitors
/ Immunohistochemistry
/ Immunotherapy
/ Inflammation
/ Lymphocytes
/ Metastases
/ Methylguanine
/ Microenvironments
/ O6-methylguanine-DNA methyltransferase
/ Oncology
/ Patients
/ PD-1 protein
/ PD-L1 protein
/ Response rates
/ Statistical analysis
/ Tumor cells
/ Tumor-infiltrating lymphocytes
/ Tumors
2021
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LAG-3 expression in the inflammatory microenvironment of glioma
Journal Article
LAG-3 expression in the inflammatory microenvironment of glioma
2021
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Overview
PurposeImmune modulatory therapies including immune checkpoint inhibitors have so far failed to result in clinically meaningful efficacy in glioma. We aimed to investigate lymphocyte activation gene 3 (LAG-3), an inhibitory receptor on immune cells and target of second-generation immune checkpoint inhibitors, in glioma.Methods97 patients with diffuse glioma (68 with glioblastoma, 29 with WHO grade II-III glioma) were identified from the Neuro-Biobank of the Medical University of Vienna. LAG-3 expression in the inflammatory microenvironment was assessed by immunohistochemistry (monoclonal anti-LAG-3 antibody, clone 17B4) and correlated to CD3+ , CD8+ , CD20+ and PD-1+ tumor-infiltrating lymphocytes (TILs) and PD-L1 expression on tumor cells.ResultsLAG-3+ TILs could be observed in 10/97 (10.3%) IDH-wildtype samples and in none of the included IDH-mutant glioma samples (p = 0.057). Further, LAG-3+ TILs were only observed in WHO grade IV glioblastoma, while none of the investigated WHO grade II–III glioma presented with LAG-3+ TILs (p = 0.03). No association of O6-methylguanine-DNA-methyltransferase (MGMT) promoter methylation and presence of LAG-3+ TILs was observed (p = 0.726). LAG-3 expression was associated with the presence of CD3+ (p = 0.029), CD8+ (p = 0.001), PD-1+ (p < 0.001) TILs and PD-L1+ tumor cells (p = 0.021), respectively. No association of overall survival with LAG-3+ TIL infiltration was evident (median OS 9.9 vs. 14.2 months, p = 0.95).ConclusionsLAG-3 is only rarely expressed on TILs in IDH-wildtype glioma and associated with active inflammatory milieu as defined by higher TIL density. Immune microenvironment diversity should be considered in the design of future immunotherapy trials in glioma.
Publisher
Springer Nature B.V
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