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Multiplexed Immunofluorescence Analysis and Quantification of Intratumoral PD-1+ Tim-3+ CD8+ T Cells
Published on: February 8, 2018
Programmed Death-Ligand 1 Expression in Non-Small Cell Lung Carcinoma Biopsies and Its Association with Tumor Infi
Background:
Immunotherapy blocking the PD-1/PD-L1 signalling pathway has become a dominant treatment modality for patients with non-small cell lung carcinoma (NSCLC). Programmed death-ligand 1 (PD-L1) expression on the membrane of tumour cells and/or tumour infiltrating lymphocytes (TIL) evaluated immunohistochemically is still the only clinically validated predictive biomarker for immunotherapy, but it has its limitations. TIL in the tumour microenviroment was identified as having predictive value. We retrospectively evaluated 134 NSCLC resection specimens, and analysed the association between PD-L1 expression, the presence of TIL, and the degree of desmoplasia in tumours.
Material And Methods:
PD-L1 expression on tumour cells and TIL were evaluated immunohistochemically using the anti-PD-L1 antibody (clone 22C3) and the anti-CD3 antibody (polyclone), respectively. PD-L1 was scored using the “tumour proportion score” (TPS) system with three categories: TPS < 1%, 1-49%, and 50%. TIL were evaluated semiquantitatively using the “percentage of stromal TIL” (PST) system, and categories of PST < 10%, 10-49% and 50% were recorded. The association between PD-L1 expression in tumour cells and TIL was compared with the PST value. Statistical analysis was conducted using the Cochran-Armitage test, and a p-value < 5% was considered significant.
Results:
PD-L1 expression was significantly higher in PST 10-49% and 50% categories than in the PST < 10% category in grade 1 and grade 2 adenocarcinomas (p = 0.008), grade 3 adenocarcinomas (p = 0.009), and squamous cell carcinomas (p = 0.028). PD-L1 expression in TIL was associated with the PST value in squamous cell carcinomas (p = 0.025) but not in adenocarcinomas. Desmoplastic tumours had particularly low TPS and PST values.
Conclusion:
PD-L1 expression in NSCLC is associated with the presence of TIL. Desmoplastic areas in tumours represent immunologically inactive tumour microenviroments. Administration of anti-PD-1/PD-L1 immunotherapy, together with agents blocking the TGF-β signalling pathway, represent a promising combinational therapy for patients with desmoplastic NSCLC. The authors declare they have no potential confl cts of interest concerning drugs, products, or services used in the study. The Editorial Board declares that the manuscript met the ICMJE recommendation for biomedical papers. Submitted: 25. 11. 2019 Accepted: 8. 12. 2019.
Insights
Programmed death-ligand 1 (PD-L1) expression in non-small cell lung carcinoma (NSCLC) correlates with tumor-infiltrating lymphocytes (TIL). Desmoplastic tumors show lower PD-L1 and TIL, suggesting immunotherapy combined with TGF-β blockade may benefit these patients.
Area of Science:
- Oncology
- Immunology
- Pathology
Background:
- Immunotherapy targeting the PD-1/PD-L1 pathway is a primary treatment for non-small cell lung carcinoma (NSCLC).
- Programmed death-ligand 1 (PD-L1) expression is the sole validated predictive biomarker for immunotherapy in NSCLC, despite limitations.
- Tumor-infiltrating lymphocytes (TIL) within the tumor microenvironment have demonstrated predictive value for immunotherapy response.
Purpose of the Study:
- To retrospectively analyze 134 NSCLC resection specimens.
- To investigate the association between PD-L1 expression, TIL presence, and tumor desmoplasia.
- To evaluate PD-L1 expression on tumor cells and TILs in relation to tumor characteristics.
Main Methods:
- Immunohistochemistry was used to assess PD-L1 expression on tumor cells and TILs (using anti-PD-L1 clone 22C3 and anti-CD3 antibody).
- PD-L1 was quantified using the tumor proportion score (TPS) (<1%, 1-49%, 50%).
- TILs were evaluated using the percentage of stromal TIL (PST) system (<10%, 10-49%, 50%), with statistical analysis via the Cochran-Armitage test.
Main Results:
- Higher PD-L1 expression was observed in tumors with PST 10-49% and 50% compared to PST <10% across adenocarcinoma and squamous cell carcinoma subtypes (p=0.008-0.028).
- PD-L1 expression in TILs correlated with PST in squamous cell carcinomas (p=0.025) but not in adenocarcinomas.
- Desmoplastic tumors exhibited significantly lower TPS and PST values.
Conclusions:
- PD-L1 expression in NSCLC is linked to the presence of TILs.
- Desmoplastic tumor areas represent immunologically less active microenvironments.
- Combination therapy with anti-PD-1/PD-L1 agents and TGF-β pathway inhibitors shows promise for desmoplastic NSCLC.
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