Systematic analysis of IL-6 as a predictive biomarker and desensitizer of immunotherapy responses in patients with non-small cell lung cancer

被引:52
|
作者
Liu, Chengming [1 ,2 ]
Yang, Lu [3 ,4 ]
Xu, Haiyan [5 ]
Zheng, Sufei [1 ,2 ]
Wang, Zhanyu [1 ,2 ]
Wang, Sihui [1 ,2 ]
Yang, Yaning [4 ]
Zhang, Shuyang [4 ]
Feng, Xiaoli [6 ]
Sun, Nan [1 ,2 ]
Wang, Yan [4 ]
He, Jie [1 ,2 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Dept Thorac Surg, Natl Canc Ctr, Natl Clin Res Ctr Canc,Canc Hosp, Beijing 100021, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, State Key Lab Mol Oncol, Natl Canc Ctr, Natl Clin Res Ctr Canc,Canc Hosp, Beijing 100021, Peoples R China
[3] Peking Univ Third Hosp, Dept Med Oncol & Radiat Sickness, Beijing 100191, Peoples R China
[4] Chinese Acad Med Sci & Peking Union Med Coll, Dept Med Oncol, Natl Canc Ctr, Natl Clin Res Ctr Canc,Canc Hosp, Beijing 100021, Peoples R China
[5] Chinese Acad Med Sci & Peking Union Med Coll, Dept Comprehens Oncol, Natl Canc Ctr, Natl Clin Res Ctr Canc,Canc Hosp, Beijing 100021, Peoples R China
[6] Chinese Acad Med Sci & Peking Union Med Coll, Dept Pathol, Natl Canc Ctr, Natl Clin Res Ctr Canc,Canc Hosp, Beijing 100021, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
NSCLC; Immune checkpoint inhibitors; IL-6; Clinical response; Resistance; IMMUNE CHECKPOINT BLOCKADE; TUMOR MICROENVIRONMENT; PD-L1; EXPRESSION; ADVERSE EVENTS; INTERLEUKIN-6; STAT3; EFFICACY; ADENOCARCINOMA; ACTIVATION; PROTEIN;
D O I
10.1186/s12916-022-02356-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Cytokines have been reported to alter the response to immune checkpoint inhibitors (ICIs) in patients with the tumor in accordance with their plasma concentrations. Here, we aimed to identify the key cytokines which influenced the responses and stimulated resistance to ICIs and tried to improve immunological response and develop novel clinical treatments in non-small cell lung cancer (NSCLC). Methods: The promising predictive cytokines were analyzed via the multi-analyte flow assay. Next, we explored the correlation baseline level of plasma cytokines and clinical outcomes in 45 NSCLC patients treated with ICIs. The mechanism of the potential candidate cytokine in predicting response and inducing resistance to ICIs was then investigated. Results: We found NSCLC with a low baseline concentration of IL-6 in plasma specimens or tumor tissues could derive more benefit from ICIs based on the patient cohort. Further analyses revealed that a favorable relationship between PD-L1 and IL-6 expression was seen in NSCLC specimens. Results in vitro showed that PD-L1 expression in the tumor was enhanced by IL-6 via the JAK1/Stat3 pathway, which induced immune evasion. Notably, an adverse correlation was found between IL-6 levels and CD8(+)T cells. And a positive association between IL-6 levels and myeloid-derived suppressor cells, M2 macrophages and regulator T cells was also seen in tumor samples, which may result in an inferior response to ICIs. Results of murine models of NSCLC suggested that the dual blockade of IL-6 and PD-L1 attenuated tumor growth. Further analyses detected that the inhibitor of IL-6 stimulated the infiltration of CD8(+)T cells and yielded the inflammatory phenotype. Conclusions: This study elucidated the role of baseline IL-6 levels in predicting the responses and promoting resistance to immunotherapy in patients with NSCLC. Our results indicated that the treatment targeting IL-6 may be beneficial for ICIs in NSCLC.
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页数:15
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