dc.contributor.author | Førde, Dagny | |
dc.contributor.author | Kilvær, Thomas Karsten | |
dc.contributor.author | Pedersen, Mona Irene | |
dc.contributor.author | Blix, Egil Støre | |
dc.contributor.author | Urbarova, Ilona Halva | |
dc.contributor.author | Paulsen, Erna-Elise | |
dc.contributor.author | Rakaee, Mehrdad | |
dc.contributor.author | Busund, Lill-Tove Rasmussen | |
dc.contributor.author | Dønnem, Tom | |
dc.contributor.author | Andersen, Sigve | |
dc.date.accessioned | 2025-01-15T08:52:40Z | |
dc.date.available | 2025-01-15T08:52:40Z | |
dc.date.issued | 2024-12-19 | |
dc.description.abstract | Introduction: Tumor-infiltrating lymphocytes are both prognostic and predictive
biomarkers for immunotherapy response. However, less is known about the
survival benefits of their subpopulations.<p>
<p>Methods: Using machine learning models, we assessed the clinical association of
the CD8+, PD1+, TCF1+ cel l subset by multiplex immunohistochemistry using
tissue microarrays in 553 non-small cell lung cancer (NSCLC) patients and its
correlation with other immune cell biomarkers.
<p>Results: We observed positive correlations between TCF1 and CD20 (r=0.37),
CD3 (r=0.45)and CD4 (r=0.33). Notably, triple positive (CD8+PD1+TCF1+) were
rare, only observed in 29 of 553 patients (5%). Our analysis revealed that cells
coexpressing TCF1 with either CD8+ or PD1+ were independent prognostic
markers of disease-specific survival in multivariable analysis (HR=0.728, p=0.029
for CD8+TCF1+, and HR=0.612, p=0.002 for PD1+TCF1+). To pilot the subtype
of abundant CD8-TCF1+ cells, we explored an immune cell infiltrated whole
slideimage and found the majority to be CD4+.
<p>Discussion: Overall, these findings suggest that assessment of CD8+, PD1+,
TCF1+ could serve as a potential prognostic biomarker in NSCLC. | en_US |
dc.identifier.citation | Førde, Kilvær, Pedersen, Blix, Urbarova, Paulsen, Rakaee, Busund, Dønnem, Andersen. High density of TCF1+ stem-like tumor-infiltrating lymphocytes is associated with favorable disease-specific survival in NSCLC. Frontiers in Immunology. 2024;15 | en_US |
dc.identifier.cristinID | FRIDAID 2339568 | |
dc.identifier.doi | 10.3389/fimmu.2024.1504220 | |
dc.identifier.issn | 1664-3224 | |
dc.identifier.uri | https://hdl.handle.net/10037/36190 | |
dc.language.iso | eng | en_US |
dc.publisher | Frontiers Media | en_US |
dc.relation.journal | Frontiers in Immunology | |
dc.rights.accessRights | openAccess | en_US |
dc.rights.holder | Copyright 2024 The Author(s) | en_US |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0 | en_US |
dc.rights | Attribution 4.0 International (CC BY 4.0) | en_US |
dc.title | High density of TCF1+ stem-like tumor-infiltrating lymphocytes is associated with favorable disease-specific survival in NSCLC | en_US |
dc.type.version | publishedVersion | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |