[Assessment of baseline CCL19+ dendritic cell infiltration for predicting responses to immunotherapy in lung adenocarcinoma patients].

M Zhu, B Wang, X Zhang, K Zhou, Z Miao, J Sun
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Abstract

Objective: To explore the correlation of baseline CCL19+ dendritic cell (CCL19+ DC) infiltration in lung adenocarcinoma microenvironment with immunotherapy efficacy and CD8+ T cell infiltration.

Methods: We retrospectively analyzed the data of patients with lung adenocarcinoma hospitalized at First Affiliated Hospital of Henan University of Science and Technology from January, 2020 to December, 2023, and collected tissue samples from 96 patients undergoing immunotherapy for assessing CCL19+ DC and CD8+ T cell infiltration using immunofluorescence assay. We evaluated the predictive value of baseline CCL19+ DCs for patient responses to immunotherapy using receiver-operating characteristics (ROC) curves and analyzed the correlations of baseline CCL19+ DC expression with immunotherapy efficacy and CD8+ T cell and cytotoxic T lymphocyte (CTL) infiltrations. In co-culture systems of lung adenocarcinoma PC9 cells, CD8+ T cells and DCs (overexpressing CCL19 with or without anti PD-1 antibody treatment), the expressions of granzyme B, perforin, IFN-γ, and Ki-67 in T cells were analyzed using flow cytometry.

Results: The patients with partial or complete remission following immunotherapy had a significantly higher baseline CCL19+ DC infiltration level in lung adenocarcinoma tissues than those with poor responses. CCL19+ DC infiltration had an area under ROC curve of 0.785, a sensitivity of 75.6%, and a specificity of 62.8% for predicting immunotherapy efficacy. The expression of CD8+ T cell surface molecules Granzyme B (P<0.01), Perforin (P<0.01), IFN-γ (P<0.01) and Ki-67 (P<0.001) in patients with high expression of CCL19+ DC were higher than those in patients with low expression of CCL19+ DC. The baseline CCL19+ DC infiltration level was positively correlated with immunotherapy efficacy (P=0.003), CTL infiltration of (r=0.6657, P<0.001) and CD8+ T cell infiltration (P=0.007). In the co-cultured cells, CCL19 overexpression combined with anti-PD1 treatment of the DCs more strongly enhanced cytotoxicity and proliferation of CD8+ T lymphocytes than either of the single treatments (P<0.01 or 0.001).

Conclusion: The baseline CCL19+ DC infiltration level in lung adenocarcinoma microenvironment is positively correlated with immunotherapy efficacy and CTL infiltration and can thus predict the response to immunotherapy.

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[评估基线 CCL19+ 树突状细胞浸润以预测肺腺癌患者对免疫疗法的反应】。]
目的探讨肺腺癌微环境中CCL19+树突状细胞(CCL19+ DC)浸润基线与免疫治疗疗效及CD8+ T细胞浸润的相关性:我们回顾性分析了2020年1月至2023年12月在河南科技大学第一附属医院住院治疗的肺腺癌患者数据,并收集了96名接受免疫治疗的患者的组织样本,采用免疫荧光法评估CCL19+ DC和CD8+ T细胞浸润。我们利用受者操作特征曲线(ROC)评估了基线CCL19+ DC对患者免疫疗法反应的预测价值,并分析了基线CCL19+ DC表达与免疫疗法疗效、CD8+ T细胞和细胞毒性T淋巴细胞(CTL)浸润的相关性。在肺腺癌PC9细胞、CD8+ T细胞和DC(过表达CCL19,抗PD-1抗体治疗或不治疗)的共培养系统中,使用流式细胞术分析了T细胞中颗粒酶B、穿孔素、IFN-γ和Ki-67的表达:结果:免疫治疗后部分或完全缓解的患者肺腺癌组织中的CCL19+ DC浸润基线水平明显高于反应差的患者。CCL19+ DC浸润在预测免疫治疗疗效方面的ROC曲线下面积为0.785,灵敏度为75.6%,特异度为62.8%。CD8+ T细胞表面分子粒酶B(PPγ)(PP+ DC)的表达高于CCL19+ DC低表达的患者。基线CCL19+ DC浸润水平与免疫治疗疗效(P=0.003)、CTL浸润(r=0.6657,P+ T细胞浸润(P=0.007)呈正相关。在共培养细胞中,CCL19 过表达与抗 PD1 处理 DCs 相比,能更强地增强 CD8+ T 淋巴细胞的细胞毒性和增殖(PConclusion:肺腺癌微环境中的基线CCL19+ DC浸润水平与免疫疗法疗效和CTL浸润呈正相关,因此可以预测免疫疗法的反应。
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