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Published on: January 19, 2019
ATAD2 is a potential immunotherapy target for patients with small cell lung cancer harboring HLA-A∗0201
Li Yuan1, Sini Li2, Yixiang Zhu1
1State 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.
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).
Insights
This study identifies the ATAD2 YSDDDVPSV immunopeptide as a promising target for small cell lung cancer (SCLC) immunotherapy. This discovery offers a new strategy for developing adoptive T cell therapies for SCLC patients.
Area of Science:
- Oncology
- Immunology
- Biochemistry
Background:
- Small cell lung cancer (SCLC) is an aggressive neuroendocrine tumor with poor prognosis.
- Effective immune-based therapies for SCLC are limited by the lack of identified tumor antigens.
Purpose of the Study:
- To identify novel tumor antigens for SCLC immunotherapy.
- To investigate the expression and potential of ATPase family AAA domain-containing protein 2 (ATAD2) as a therapeutic target.
Main Methods:
- Liquid chromatography-tandem mass spectrometry (LC-MS/MS) was used to analyze cancer/testis antigens (CTAs) in SCLC.
- Immunohistochemistry and RNA sequencing were employed to assess ATAD2 expression in SCLC and other lung cancers.
- Immunopeptidomics identified specific ATAD2-derived epitopes for T cell recognition.
Main Results:
- ATAD2 was significantly overexpressed in SCLC compared to normal tissues and non-small cell lung cancer (NSCLC).
- The ATAD2-derived peptide YSDDDVPSV (HLA-A*02:01 restricted) was identified as a promising tumor antigen.
- HLA-A*02:01 T cells showed a robust response to the YSDDDVPSV immunopeptide.
Conclusions:
- The ATAD2 YSDDDVPSV immunopeptide represents a potential target for SCLC immunotherapy.
- This finding supports the development of adoptive T cell therapies for ASCL1-positive or NEUROD1-positive SCLC with HLA-A*02:01.
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