4.7 Article

Tobacco exposure primes the secretion of CCL21 positively associated with tertiary lymphoid structure and response to immunotherapy

Journal

JOURNAL FOR IMMUNOTHERAPY OF CANCER
Volume 11, Issue 6, Pages -

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/jitc-2023-006939

Keywords

biomarkers; tumor; cytokines; immunotherapy; non-small cell lung cancer

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Smoking history is associated with increased levels of tertiary lymphoid structures and chemokine CCL21, which impacts the efficacy of immunotherapy in patients with lung cancer. Tobacco exposure promotes CCL21 expression and enhances the interaction between CD4+T cells and CD20+B cells through the CCL21/CCR7 axis, leading to the formation of tertiary lymphoid structures. Furthermore, serum levels of CCL21 can serve as a reliable biomarker for predicting the efficacy of immunotherapy.
BackgroundIt has been reported that smoking history as a predictor of immunotherapy efficacy in patients with advanced lung cancer, however, the underlying mechanisms of this phenomenon remain largely unknown. MethodsThe patients with lung adenocarcinoma's (LUAD) cohort and the orthotopical transplanted mouse model were used to explore the correlation between smoking status and tertiary lymphoid structure (TLS) and chemokine CCL21, respectively. Cell adhesion and co-immunoprecipitation assays were performed to explore the interaction between CD4+T cells and CD20+B cells under tobacco exposure. Chromatin immunoprecipitation-PCR was used to dissect the mechanism of upregulated CCL21 secretion in tobacco treatment. Serum CCL21 level was recorded in patients with LUAD treated with immunotherapy. ResultsHere we observed that individuals with a smoking history exhibit an increased quantity and maturation level of TLS compared with non-smokers, along with higher levels of CCL21 secretion. Tobacco exposure promoted CCL21 expression in an epithelial cell-intrinsic manner, of which BaP, the main component of tobacco, facilitated the nuclear retention of the aryl hydrocarbon receptor that occupied the promoter of CCL21. Additionally, the activated CCL21/CCR7 axis increased the CD11a expression of CD4+T cells, boosting the interaction with CD20+B cells dependent on ICAM1, which potentially induced the TLSs formation. Patients with elevated serum levels of CCL21 benefited more from immunotherapy. ConclusionsPatients with a smoking history exhibited higher levels of TLS via the CCL21-dependent mechanism, serum CCL21 was identified as a reliable biomarker for predicting the efficacy of immunotherapy.

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