Circulating stem-like exhausted CD8 T cells point to better outcomes in lung cancer: a brief report.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
30 patients with advanced NSCLC and assessed their correlation with OS.
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
As shown previously in PE, Tex cells in the blood did not correlate with OS. Our results further support the importance of Tex in the anti-cancer immune response and provide useful evidence for the utility of peripheral blood sampling for future studies examining exhausted T cells (Tex).
Anti-cancer T cells exhibit a spectrum of functional abilities and exhaustion levels and can be broadly categorized as stem-like exhausted T cells (Tex) that retain cancer-killing capacity, and termin
- p-value P=0.006
- p-value P=0.002
APA
Ye L, Dick I, et al. (2025). Circulating stem-like exhausted CD8 T cells point to better outcomes in lung cancer: a brief report.. Translational lung cancer research, 14(11), 5074-5081. https://doi.org/10.21037/tlcr-2025-509
MLA
Ye L, et al.. "Circulating stem-like exhausted CD8 T cells point to better outcomes in lung cancer: a brief report.." Translational lung cancer research, vol. 14, no. 11, 2025, pp. 5074-5081.
PMID
41367566 ↗
Abstract 한글 요약
Anti-cancer T cells exhibit a spectrum of functional abilities and exhaustion levels and can be broadly categorized as stem-like exhausted T cells (Tex) that retain cancer-killing capacity, and terminally exhausted T cells (Tex) with limited function. Previously, we identified CD8 Tex and Tex cells in malignant pleural effusions (PEs) of non-small cell lung cancer (NSCLC) and mesothelioma patients. In both cancers, increased frequency of Tex cells was associated with improved overall survival (OS). However, not all cancer patients develop PE, and sampling of PE is invasive, with associated risks. In this study we sought to determine if Tex and Tex cells in the blood of patients with NSCLC also associated with survival. Using flow cytometry, we quantified Tex and Tex in blood samples from 30 patients with advanced NSCLC and assessed their correlation with OS. In half of these cases, we also analyzed matched PE samples for comparison. Compared to PE, peripheral blood had a lower frequency of Tex (3.8% 9.4% of CD8 T cells, P=0.006) and Tex (0.3% 1.1%, P=0.002). However, both subsets were significantly correlated between the two sites (Tex r=0.82, P<0.001; Tex r=0.63, P=0.01). Higher Tex cell frequency in the blood was associated with improved survival after adjusting for potentially prognostic patient and tumor related factors. When stratified into high and low groups based on the median, higher Tex cells levels correlated with better OS [hazard ratio (HR) 0.16, 95% confidence interval (CI): 0.03-0.10, P=0.048]. As shown previously in PE, Tex cells in the blood did not correlate with OS. Our results further support the importance of Tex in the anti-cancer immune response and provide useful evidence for the utility of peripheral blood sampling for future studies examining exhausted T cells (Tex).
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