一种用于克服非小细胞肺癌治疗中抗原异质性的多靶向 CAR-T 细胞平台
A Multi-Targeting Chimeric Antigen Receptor-T Cell Platform to Overcome Antigen Heterogeneity in the Treatment of Non-Small Cell Lung Cancer.
这些发现支持采用多靶点CAR-T 策略来应对NSCLC及可能其他实体瘤中的抗原异质性。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:SFTPA1 is a potential prognostic biomarker correlated with immune cell infiltration and response to immunotherapy in lung adenocarcinoma.
SFTPA1 is a potential prognostic biomarker correlated with immune cell infiltration and response to immunotherapy in lung adenocarcinoma.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
肺表面活性蛋白A1(SFTPA1)是C型凝集素亚家族的成员,在维持肺组织稳态和先天免疫反应中发挥关键作用。SFTPA1的破坏可导致多种急性或慢性肺部疾病,包括肺癌。
然而,目前很少有研究将SFTPA1与肺癌中的免疫细胞浸润及免疫治疗反应相关联。本研究的结果描述了SFTPA1在多个数据库中的表达谱,并通过免疫组化实验在BALB/c小鼠、人类肿瘤组织及配对正常组织中进行了验证。通过对TCGA中肺腺癌(LUAD)样本的生存分析发现,SFTPA1 mRNA高表达与良好预后相关。
进一步的基因本体论(GO)和京都基因与基因组百科全书(KEGG)通路富集分析表明,SFTPA1参与toll样受体信号通路。免疫浸润分析阐明,SFTPA1高表达与M1巨噬细胞、CD8+ T细胞、记忆活化CD4+ T细胞、调节性T细胞数量增加以及M2巨噬细胞数量减少相关。
我们的临床数据表明,SFTPA1可能作为预测LUAD患者免疫治疗良好反应的生物标志物。总之,我们的研究拓展了SFTPA1的表达谱和潜在调控通路,并可能为建立肺腺癌新型预防和治疗策略提供潜在的生物标志物。
Pulmonary surfactant protein A1 (SFTPA1) is a member of the C-type lectin subfamily that plays a critical role in maintaining lung tissue homeostasis and the innate immune response. SFTPA1 disruption can cause several acute or chronic lung diseases, including lung cancer.
However, little research has been performed to associate SFTPA1 with immune cell infiltration and the response to immunotherapy in lung cancer. The findings of our study describe the SFTPA1 expression profile in multiple databases and was validated in BALB/c mice, human tumor tissues, and paired normal tissues using an immunohistochemistry assay. High SFTPA1 mRNA expression was associated with a favorable prognosis through a survival analysis in lung adenocarcinoma (LUAD) samples from TCGA.
Further GeneOntology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses showed that SFTPA1 was involved in the toll-like receptor signaling pathway. An immune infiltration analysis clarified that high SFTPA1 expression was associated with an increased number of M1 macrophages, CD8 + T cells, memory activated CD4 + T cells, regulatory T cells, as well as a reduced number of M2 macrophages.
Our clinical data suggest that SFTPA1 may serve as a biomarker for predicting a favorable response to immunotherapy for patients with LUAD. Collectively, our study extends the expression profile and potential regulatory pathways of SFTPA1 and may provide a potential biomarker for establishing novel preventive and therapeutic strategies for lung adenocarcinoma.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。