γδ T 细胞调节小细胞肺癌中的抗肿瘤免疫
γδ T cells modulate anti-tumor immunity in small cell lung cancer.
我们的发现表明,活化的γδ T细胞可能是SCLC治疗的有价值靶点。
英文原题:ATAD2 is a potential immunotherapy target for patients with small cell lung cancer harboring HLA-A∗0201.
ATAD2 is a potential immunotherapy target for patients with small cell lung cancer harboring HLA-A∗0201.
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。
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。
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).
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