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ATAD2 是携带 HLA-A∗0201 的小细胞肺癌患者的潜在免疫治疗靶点

英文原题:ATAD2 is a potential immunotherapy target for patients with small cell lung cancer harboring HLA-A∗0201.

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ATAD2 is a potential immunotherapy target for patients with small cell lung cancer harboring HLA-A∗0201.

PubMed 2025/01/13(内容时间) EBioMedicine Q1 · IF 11.2(JCR 2025)

研究概要

我们的发现凸显了靶向ATAD2 YSDDDVPSV免疫肽用于SCLC免疫治疗的潜力,从而为开发过继性T细胞疗法以有效治疗携带HLA-A∗02:01的ASCL1阳性或NEUROD1阳性SCLC提供了一条有前景的途径。

研究思路结论见上方概要

小细胞肺癌(SCLC)是一种高度侵袭性的神经内分泌肿瘤,预后极差。目前,尚难以确定能够促进SCLC免疫治疗的特定肿瘤抗原。

我们采用液相色谱-串联质谱法(LC-MS/MS)分析了SCLC细胞系和人类肿瘤标本中的癌/睾丸抗原(CTAs)。对临床标本进行免疫组织化学染色,以比较SCLC、非小细胞肺癌(NSCLC)及匹配的癌旁正常组织中的蛋白表达。此外,我们还查询了公开可用的RNA测序数据库,以识别不同SCLC亚型及不同疾病阶段中的基因表达模式。

在SCLC各亚型中鉴定出不同数量和类型的CTA,与正常癌旁组织和NSCLC组织相比,SCLC中ATPase家族AAA结构域含蛋白2(ATAD2)的表达水平显著升高。在SCLC的整个临床过程中发现ATAD2呈动态表达模式,并与SCLC中achaete-scute家族bHLH转录因子1(ASCL1)的表达呈正相关。免疫肽组学分析鉴定出源自ATAD2的HLA-A∗02:01限制性表位的YSDDDVPSV序列,作为潜在免疫治疗应用的高度有前景的肿瘤抗原候选物。YSDDDVPSV免疫肽被证实存在于具有HLA-A∗02:01限制性的SCLC-A和SCLC-N中。值得注意的是,HLA-A∗02:01 T细胞在经T2细胞呈递的YSDDDVPSV免疫肽刺激后表现出强烈的应答。

展开英文摘要原文

BACKGROUND: Small cell lung cancer (SCLC) represents a highly aggressive neuroendocrine tumour with a dismal prognosis. Currently, the identification of a specific tumour antigen that can facilitate immune-based therapies for SCLC remains elusive. METHODS: We employed liquid chromatography-tandem mass spectrometry (LC-MS/MS) to analyse cancer/testis antigens (CTAs) in SCLC cell lines and human tumour specimens. Immunohistochemistry of clinical specimens was performed to compare protein expression in SCLC, non-small cell lung cancer (NSCLC), and matched normal-adjacent tissues. Additionally, publicly available RNA sequencing databases were interrogated to identify gene expression patterns in different SCLC subtypes and in different disease stages. FINDINGS: Distinct numbers and types of CTAs were identified across SCLC subtypes, with significantly higher expression levels of ATPase family AAA domain-containing protein 2 (ATAD2) observed in SCLC compared to normal adjacent tissues and NSCLC tissues. A dynamic expression pattern of ATAD2 was found throughout the clinical course of SCLC and exhibited a positive correlation with achaete-scute family bHLH transcription factor 1 (ASCL1) expression in SCLC. Immunopeptidomics analysis identified the YSDDDVPSV sequence derived from the HLA-A∗02:01 restriction epitope of ATAD2 as a highly promising tumour antigen candidate for potential immunotherapy applications. YSDDDVPSV immunopeptides were confirmed to be present in SCLC-A and SCLC-N with HLA-A∗02:01 restriction. Notably, HLA-A∗02:01 T cells exhibited a robust response upon stimulation with YSDDDVPSV immunopeptide pulsed by T2 cells. INTERPRETATION: Our findings highlight the potential of targeting the ATAD2 YSDDDVPSV immunopeptide for SCLC immunotherapy, thereby offering a promising avenue for the development of adoptive T cell therapies to effectively treat ASCL1-positive or NEUROD1-positive SCLC carrying HLA-A∗02:01. FUNDING: This study was supported by the National key R&D program of China (2022YFC2505000); National Natural Science Foundation of China (NSFC) general program (82272796) NSFC special program (82241229); CAMS Innovation Fund for Medical Sciences (CIFMS 2022-I2M-1-009); CAMS Key Laboratory of Translational Research on Lung Cancer (2018PT31035); Aiyou foundation (KY201701). National key R&D program of China (2022YFC2505004). NSFC general program (81972905). Medical Oncology Key Foundation of Cancer Hospital Chinese Academy of Medical Sciences (CICAMS-MOCP2022012).

论文信息

作者
Yuan L、Li S、Zhu Y、Yang L、Zhang X、Qu Y、Wang Z、Duan J
第一作者单位
State Key Laboratory of Molecular Oncology, CAMS Key Laboratory of Translational Research on Lung Cancer, Department of Medical Oncology, National Cancer Centre/National Clinical Research Centre for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences Peking Union Medical College, Beijing, 100021, China.China
通讯作者单位
State Key Laboratory of Molecular Oncology, CAMS Key Laboratory of Translational Research on Lung Cancer, Department of Medical Oncology, National Cancer Centre/National Clinical Research Centre for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences Peking Union Medical College, Beijing, 100021, China. Electronic address: zlhuxi@163.com.China
期刊
EBioMedicine2025 Feb
原文标识
PubMed 39808946 · DOI 10.1016/j.ebiom.2024.105515