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Updated: Jul 11, 2025

Multiplexed Immunofluorescence Analysis and Quantification of Intratumoral PD-1+ Tim-3+ CD8+ T Cells
Published on: February 8, 2018
TIM-3 expression induces resistance to PD-1 inhibitor in G-CSF-producing lung spindle cell carcinoma: A case report
Fumiko Hayashi1, Kazumasa Akagi2,3, Hirokazu Taniguchi2,3
1Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.
Abstract:
Lung spindle cell carcinoma is an aggressive subtype of pleomorphic lung cancer resistant to cytotoxic chemotherapy. Programmed cell death-1 (PD-1) inhibitors have been reported to have clinical effects in patients with spindle cell carcinoma; however, the resistance mechanism to PD-1 inhibitors is yet to be fully elucidated. Herein, we report the case of an 88-year-old man with G-CSF-producing spindle cell carcinoma who acquired resistance to PD-1/PD-ligand 1 (L1) inhibitor in an early setting after a remarkable response. A histopathological review of the resistant specimen revealed a low count of CD8+ T cells and a predominant presence of M2 and TIM-3+ macrophages, indicating the presence of an immunosuppressive microenvironment. Our findings suggest a novel resistance mechanism to PD-1/PD-L1 inhibitors in G-CSF-producing spindle cell carcinoma.
Insights
This study explores resistance to programmed cell death-1 (PD-1) inhibitors in G-CSF-producing lung spindle cell carcinoma. Findings reveal an immunosuppressive microenvironment with M2 and TIM-3+ macrophages as a novel resistance mechanism.
Area of Science:
- Oncology
- Immunology
- Pathology
Background:
- Lung spindle cell carcinoma is an aggressive, chemotherapy-resistant lung cancer subtype.
- Programmed cell death-1 (PD-1) inhibitors show promise, but resistance mechanisms are unclear.
- Granulocyte-colony stimulating factor (G-CSF)-producing spindle cell carcinoma presents unique challenges.
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