| Publisher Information: |
Umeå universitet, Umeå Centre for Microbial Research (UCMR); Umeå universitet, Institutionen för molekylärbiologi (Medicinska fakulteten); Umeå universitet, Institutionen för molekylärbiologi (Teknisk-naturvetenskaplig fakultet); Hellenic Oncology Research Group (HORG), Athens, United States; Laboratory of Oncology, Faculty of Medicine, School of Health Sciences, University of Thessaly, Greece; Department of Medical Oncology, University General Hospital of Larissa, Greece; St. John's Institute of Dermatology, School of Basic and Medical Biosciences and KHP Centre for Translational Medicine, King's College London, United Kingdom, Guy's Hospital, London, United Kingdom; Breast Cancer Now Research Unit, School of Cancer and Pharmaceutical Sciences, King's College London, Guy's Cancer Centre, United Kingdom, London, United Kingdom; Department of Informatics, Faculty of Natural, Mathematical and Engineering Sciences, King's College London, United Kingdom, London, United Kingdom; Hellenic Oncology Research Group (HORG), Athens, United States; Biomedical Research Foundation of the Academy of Athens, Athens, United States; Medical School, University of Cyprus, Nicosia, Cyprus; 2nd Department of Pathology, "Attikon" University Hospital, Medical School, National and Kapodistrian University of Athens, Athens, United States; St. John's Institute of Dermatology, School of Basic and Medical Biosciences and KHP Centre for Translational Medicine, King's College London, United Kingdom, Guy's Hospital, London, United Kingdom; Department of Informatics, Faculty of Natural, Mathematical and Engineering Sciences, King's College London, United Kingdom, London, United Kingdom; Department of Pathology, 'Sotiria' General Hospital for Chest Diseases, Athens, United States; Department of Pathology, Metropolitan Hospital, Athens, United States; St. John's Institute of Dermatology, School of Basic and Medical Biosciences and KHP Centre for Translational Medicine, King's College London, United Kingdom, Guy's Hospital, London, United Kingdom; Breast Cancer Now Research Unit, School of Cancer and Pharmaceutical Sciences, King's College London, Guy's Cancer Centre, United Kingdom, London, United Kingdom |
| Description: |
Background: The spatial distribution and functional heterogeneity of tumor-infiltrating lymphocytes (TILs) significantly impact patient outcomes in non-small cell lung cancer (NSCLC). While T cell factor 1 (TCF1) expressing TILs have emerged as key players in sustaining anti-tumor immunity, their subset characterization, localization, and clinical significance within the tumor microenvironment remain poorly defined. Method: We performed multiplex immunohistochemistry and immunofluorescence to characterize TCF1+ immune cell subsets, in 102 NSCLC tumors, separately analyzing the tumor center (TC) and invasive front (IF). We integrated this data with publicly available single-cell RNA-sequencing datasets and clinical outcome analyses. Results: CD4+ T cells and CD79α+ B cells, dominate the TCF1+ landscape, while CD8+ T cells constitute a minority of TCF1+ immune cells, particularly in the TC. We demonstrated the presence of tumor-infiltrating IgG+/IgA+ plasma cells co-expressing TCF1. PD1+TCF1- cells were more frequent than PD1+TCF1+ cells both in the TC and IF, reflecting that terminally differentiated exhausted TILs predominate within the tumor microenvironment. Survival analyses revealed significantly different prognostic impact of TILs including TCF1-expressing cells based on topography. Multivariate analysis showed that increased CD8+TCF1+ cells (HR: 2.5; p=0.039) and increased TCF1 expression by cancer cells (HR: 2,7; p=0.041) in the TC and CD4+TCF1+ cells (HR: 0.4; p=0.043) in the IF emerged as negative and positive independent prognostic markers for Disease-free survival (DFS), respectively. Integrating PD-L1 expression with TILs, PD-L1 immunopositivity was correlated with increased CD8+ and PD1+TCF1- cell infiltration and was associated with favorable DFS especially in the TC. Conclusions: Our findings support a more refined framework for TCF1+ TIL assessment and TCF1 expression across cellular populations in the tumor microenvironment, with implications for prognostication in operable NSCLC. |