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Lung tissue T cells are activated in chronic obstructive pulmonary disease with non-small cell lung cancer patients.

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Scientific reports 📖 저널 OA 96.2% 2021: 24/24 OA 2022: 32/32 OA 2023: 45/45 OA 2024: 140/140 OA 2025: 938/938 OA 2026: 692/767 OA 2021~2026 2025 Vol.15(1) p. 41209
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유사 논문
P · Population 대상 환자/모집단
환자: COPD have been shown to exhibit favorable responses to anti-PD-1/PD-L1 therapy
I · Intervention 중재 / 시술
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C · Comparison 대조 / 비교
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O · Outcome 결과 / 결론
Furthermore, the abundance of CD103 T cells in non-tumor lung tissues correlated with IFN-γ production and COPD-related clinical parameters (pack-years smoking history and the FEV1/FVC ratio). In NSCLC patients with COPD, T cells were active participants in both the non-tumor and the lung tumor tissues, suggesting the potential response to immunotherapy.

Tone M, Isono T, Yamamoto Y, Takeda Y, Shintani Y, Kumanogoh A, Wada H, Iwahori K

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Chronic obstructive pulmonary disease (COPD) is characterized by chronic inflammation of the respiratory tract and is associated with an increased risk of lung cancer.

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APA Tone M, Isono T, et al. (2025). Lung tissue T cells are activated in chronic obstructive pulmonary disease with non-small cell lung cancer patients.. Scientific reports, 15(1), 41209. https://doi.org/10.1038/s41598-025-25141-x
MLA Tone M, et al.. "Lung tissue T cells are activated in chronic obstructive pulmonary disease with non-small cell lung cancer patients.." Scientific reports, vol. 15, no. 1, 2025, pp. 41209.
PMID 41271981 ↗

Abstract

Chronic obstructive pulmonary disease (COPD) is characterized by chronic inflammation of the respiratory tract and is associated with an increased risk of lung cancer. Non-small cell lung cancer (NSCLC) patients with COPD have been shown to exhibit favorable responses to anti-PD-1/PD-L1 therapy. In the present study, we investigated T cell profiles and functions in the lung tissues of NSCLC patients with or without COPD to provide the rationale for immunotherapy of NSCLC patients with COPD. Abundant PD-1 and Tim-3 T cells were detected in the lung tumor tissues of NSCLC patients with COPD. On the other hand, CD103 tissue-resident memory T (T) cells in non-tumor lung tissues were more abundant in NSCLC patients with than in those without COPD. Furthermore, the abundance of CD103 T cells in non-tumor lung tissues correlated with IFN-γ production and COPD-related clinical parameters (pack-years smoking history and the FEV1/FVC ratio). In NSCLC patients with COPD, T cells were active participants in both the non-tumor and the lung tumor tissues, suggesting the potential response to immunotherapy.

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