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:Multiomics Analysis Reveals Distinct Immunogenomic Features of Lung Cancer with Ground-Glass Opacity.
Multiomics Analysis Reveals Distinct Immunogenomic Features of Lung Cancer with Ground-Glass Opacity.
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。
为这些影像学上独特的临床实体的治疗提供机制性见解。
我们启动了一项前瞻性队列研究,收集并表征具有GGO成分(非实性和部分实性结节)或不具有GGO成分的肺结节,并通过三维图像重建精确量化,以描绘与GGO相关的分子和免疫特征。通过靶向基因panel测序、RNA测序、TCR(T细胞受体)测序和循环肿瘤DNA检测进行多组学评估。测量和主要结果:GGO相关肺癌表现出比实性结节更低的肿瘤突变负荷。转录组分析显示,GGO成分中免疫环境和免疫通路活性较低,免疫激活标志物表达降低,大多数免疫细胞亚群浸润较少,这通过多重免疫荧光得到证实。此外,T细胞库测序显示GGO相关肺癌中T细胞扩增较低。HLA杂合性缺失在具有GGO成分的肺腺癌中显著不如不具有GGO成分的肺腺癌常见。循环肿瘤DNA分析表明,肿瘤DNA向外周血的释放与非GGO成分的肿瘤大小相关。
与表现为实性肺结节的肺癌相比,GGO相关肺癌的特征是代谢活性较低、免疫微环境活性较低,这可能是其惰性临床病程的机制。临床试验注册于www.ClinicalTrials.gov(NCT03320044)。
Rationale: Ground-glass opacity (GGO)-associated lung cancers are common and radiologically distinct clinical entities known to have an indolent clinical course and superior survival, implying a unique underlying biology.
However, the molecular and immune characteristics of GGO-associated lung nodules have not been systemically studied. Objectives: To provide mechanistic insights for the treatment of these radiologically distinct clinical entities. Methods: We initiated a prospective cohort study to collect and characterize pulmonary nodules with GGO components (nonsolid and part-solid nodules) or without GGO components, as precisely quantified by using three-dimensional image reconstruction to delineate the molecular and immune features associated with GGO.
Multiomics assessment conducted by using targeted gene panel sequencing, RNA sequencing, TCR (T-cell receptor) sequencing, and circulating tumor DNA detection was performed. Measurements and Main Results: GGO-associated lung cancers exhibited a lower tumor mutation burden than solid nodules. Transcriptomic analysis revealed a less active immune environment in GGO components and immune pathways, decreased expression of immune activation markers, and less infiltration of most immune-cell subsets, which was confirmed by using multiplex immunofluorescence.
Furthermore, T-cell repertoire sequencing revealed lower T-cell expansion in GGO-associated lung cancers. HLA loss of heterozygosity was significantly less common in lung adenocarcinomas with GGO components than in those without. Circulating tumor DNA analysis suggested that the release of tumor DNA to the peripheral blood was correlated with the tumor size of non-GGO components.
Conclusions: Compared with lung cancers presenting with solid lung nodules, GGO-associated lung cancers are characterized by a less active metabolism and a less active immune microenvironment, which may be the mechanisms underlying their indolent clinical course. Clinical trial registered with www. clinicaltrials. gov (NCT03320044).
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