Expression of TILs and Patterns of Gene Expression from Paired Samples of Malignant Pleural Mesothelioma (MPM) Patients

Author:

Cedres Susana1ORCID,Serna Garazi2ORCID,Gonzalez-Medina Alberto3,Valdivia Augusto1,Assaf-Pastrana Juan David1,Iranzo Patricia1,Callejo Ana1,Pardo Nuria1,Navarro Alejandro1,Martinez-Marti Alex1,Priano Ilaria1,Fasani Roberta2,Guardia Xavier2ORCID,Gonzalo Javier4,Carbonell Caterina5,Frigola Joan5,Amat Ramon5ORCID,Navarro Victor6ORCID,Dienstmann Rodrigo6,Vivancos Ana3,Nuciforo Paolo2,Felip Enriqueta1

Affiliation:

1. Vall d’Hebron Institute of Oncology (VHIO), Hospital Universitari Vall d’Hebron, 08035 Barcelona, Spain

2. Molecular Oncology Group, Vall d’Hebron Institute of Oncology (VHIO), 08035 Barcelona, Spain

3. Cancer Genomics Lab, Vall d’Hebron Institute of Oncology (VHIO), 08035 Barcelona, Spain

4. Vall d’Hebron Institute of Oncology (VHIO), 08035 Barcelona, Spain

5. Clinical Research Department, Vall d’Hebron Institute of Oncology (VHIO), Passeig Vall d’Hebron 119-129, 08035 Barcelona, Spain

6. Oncology Data Science Group, Vall d’Hebron Institute of Oncology (VHIO), 08035 Barcelona, Spain

Abstract

MPM is an aggressive disease with an immunosuppressive tumor microenvironment, and interest in exploring immunotherapy in this disease has been increasing. In the first line of treatment, the combination of nivolumab and ipilimumab demonstrated an improvement in survival over chemotherapy. The presence of TILs has been recognized as a marker of antitumor immune response to chemotherapy in solid tumors. The aim of our study is to identify the effect of treatment on immune cells and the immune gene profile in MPM. We investigated the changes in expression of TILs in 10 human MPM paired tumor tissues using immunohistochemistry and gene expression analysis from paired untreated and treated samples. In this small series, we demonstrated that during the evolution of disease without any treatment there was an increase in the inflammatory component in tumor samples. After systemic treatment there was a decrease in the number of TILs. We observed that after systemic treatment or disease progression immune gene signatures were suppressed. Our integrated analysis of paired samples with immune profile and genomic changes on MPM suggested that during the evolution of the disease the immune system tends to switch, turning off with treatment.

Funder

Fundación AECC

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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