TCF-1+ PD-1+ CD8+T cells are associated with the response to PD-1 blockade in non-small cell lung cancer patients

被引:6
|
作者
Fang, Xia [1 ]
Wu, Gang [2 ]
Hua, Jing [1 ]
Zhao, Pei [1 ]
Shan, Mengtian [1 ]
Wang, Na [1 ]
Zeng, Yu [3 ]
Ding, Tingting [4 ]
Zhu, Hailong [5 ]
Zhu, Xuyou [3 ]
Zhang, Long [3 ]
Liu, Yuting [3 ]
Zheng, Ling [6 ]
Yi, Xianghua [3 ]
Gao, Shaoyong [1 ]
机构
[1] Tongji Univ, Sch Med, Shanghai East Hosp, Dept Resp & Crit Care Med, Shanghai, Peoples R China
[2] Tongji Univ, Sch Med, Shanghai Tongji Hosp, Dept Urol Surg, Shanghai, Peoples R China
[3] Tongji Univ, Sch Med, Shanghai Tongji Hosp, Dept Pathol, Shanghai, Peoples R China
[4] Tongji Univ, Sch Med, Shanghai Peoples Hosp 10, Dept Pathol, Shanghai, Peoples R China
[5] Fudan Univ, Sch Med, Shanghai Canc Ctr, Dept Oncol,Minhang Branch, Shanghai, Peoples R China
[6] Tongji Univ, Sch Med, Shanghai Tongji Hosp, Dept Resp & Crit Care Med, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
Non-small cell lung cancer; PD-1; immunotherapy; TCF-1(+)PD-1(+)CD8(+)T cells; Response; IMMUNOTHERAPY;
D O I
10.1007/s00432-021-03845-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To determine whether TCF-1(+)PD-1(+)CD8(+)T cells are associated with the response to PD-1 blockade in non-small cell lung cancer (NSCLC) patients. Methods We investigated the expression of TCF-1(+)PD-1(+)CD8(+)T cells and elucidated their predictive role in NSCLC patients. Pretreatment specimens from 20 advanced NSCLC patients who underwent PD-1 immunotherapy or combined with chemotherapy were analyzed. The frequencies of TCF-1(+) cells in PD-1(+)CD8(+)T cells were determined in these biospecimens using multi-label immunofluorescence staining and multi-spectral acquisition technology. The clinical roles of TCF-1(+)PD-1(+)CD8(+)T cells were assessed via analyzing our cases and human NSCLC data collected from public databases. Results A high frequency of TCF-1(+)PD-1(+)CD8(+)T cells was identified in responders compared with non-responders (p = 0.0024), and the patients with high expression of this cell subset had durable clinical benefit of anti-PD-1 therapy. There were no significant association between the expression of TCF-1(+)PD-1(+)CD8(+)T cells and patients' age, smoking history, pathologic type, and genetic status. In univariate analysis by the Cox hazard model, high frequency of TCF-1(+) PD-1(+) CD8(+)T cells was significantly correlated with patients' benefit of PD-1 blockade (p = 0.024). Conclusion Our study indicated that TCF-1(+)PD-1(+)CD8(+)T cells are associated with the response to PD-1 blockade, and may be a predictor of anti-PD-1 therapy.
引用
收藏
页码:2653 / 2660
页数:8
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