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Single-cell mapping reveals several immune subsets associated with liver metastasis of pancreatic ductal adenocarcinoma.
Zhang, Ze; Zhu, Xiao-Qiang; Yang, Feng; Lai, Nan-Nan; Zhu, Le; Cole, Kathryn; Hu, Bei-Yuan; Li, Tian-En; Zhu, Ying; Zhang, Lu-Min; Wang, Shun; Zheng, Yan; Mao, Huarong; Zhao, Yue; Bruns, Christiane; Vago, Razi; Tu, Bo; Wong, Jason W H; Fu, De-Liang; Qin, Lun-Xiu; Dong, Qiong-Zhu.
Afiliação
  • Zhang Z; Department of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
  • Zhu XQ; State Key Laboratory for Oncogenes and Related Genes, Division of Gastroenterology and Hepatology, Key Laboratory of Gastroenterology and Hepatology, Ministry of Health, Shanghai Institute of Digestive Disease, NHC Key Laboratory of Digestive Diseases, Renji Hospital, School of Medicine, Shanghai Ji
  • Yang F; Department of Pancreatic Surgery, Huashan Hospital, Fudan University, Shanghai, China.
  • Lai NN; Key Laboratory of Whole-period Monitoring and Precise Intervention of Digestive Cancer, Minhang Hospital, Fudan University, Shanghai, China.
  • Zhu L; Department of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
  • Cole K; Division of Oncology and Hematology, University of Nebraska Medical Center, Omaha, NE, USA.
  • Hu BY; Department of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
  • Li TE; Department of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
  • Zhu Y; Department of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
  • Zhang LM; Key Laboratory of Whole-period Monitoring and Precise Intervention of Digestive Cancer, Minhang Hospital, Fudan University, Shanghai, China.
  • Wang S; Department of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
  • Zheng Y; Department of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
  • Mao H; Key Laboratory of Whole-period Monitoring and Precise Intervention of Digestive Cancer, Minhang Hospital, Fudan University, Shanghai, China.
  • Zhao Y; General, Visceral and Cancer Surgery, University Hospital of Cologne, Cologne, Germany.
  • Bruns C; General, Visceral and Cancer Surgery, University Hospital of Cologne, Cologne, Germany.
  • Vago R; Department of Biotechnology Engineering, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
  • Tu B; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA. Electronic address: tutumakmdanderson@gmail.com.
  • Wong JWH; School of Biomedical Sciences, Li Ka Shing Faculty of Medicine, the University of Hong Kong, Hong Kong, China. Electronic address: jwhwong@hku.hk.
  • Fu DL; Department of Pancreatic Surgery, Huashan Hospital, Fudan University, Shanghai, China. Electronic address: surgeonfu@163.com.
  • Qin LX; Department of General Surgery, Huashan Hospital, Fudan University, Shanghai, China. Electronic address: qinlx@fudan.edu.cn.
  • Dong QZ; Department of General Surgery, Huashan Hospital, Fudan University, Shanghai, China; Key Laboratory of Whole-period Monitoring and Precise Intervention of Digestive Cancer, Minhang Hospital, Fudan University, Shanghai, China. Electronic address: qzhdong@fudan.edu.cn.
Med ; 4(10): 728-743.e7, 2023 Oct 13.
Article em En | MEDLINE | ID: mdl-37633269
BACKGROUND: Identifying a metastasis-correlated immune cell composition within the tumor microenvironment (TME) of pancreatic ductal adenocarcinoma (PDAC) will help to develop promising and innovative therapeutic strategies. However, the dynamics of immune cell lineages in the TME of advanced PDAC remains elusive. METHODS: Twenty-six samples from 11 patients (including 11 primary tumor tissues, 10 blood, and 5 lymph nodes) with different stages were used to develop a multiscale immune profile. High-dimensional single-cell analysis with mass cytometry was performed to search for metastasis-correlated immune changes in the microenvironment. The findings were further validated by published single-cell RNA sequencing (scRNA-seq) data and multiplex fluorescent immunohistochemistry. FINDINGS: High-dimensional single-cell profiling revealed that the three immune-relevant sites formed a distinct immune atlas. Interestingly, the PDAC microenvironment with the potential for metastatic spread to the liver was characterized by a decreased proportion of CD103+PD-1+CD39+ T cells with cytotoxic and exhausted functional status and an increased proportion of CD73+ macrophages. Analysis of scRNA-seq data of PDAC further confirmed the identified subsets and revealed strong potential interactions via various ligand-receptor pairs between the identified T subsets and the macrophages. Moreover, stratified patients with different immune compositions correlated with clinical outcomes of PDAC. CONCLUSIONS: Our study uncovered metastasis-correlated immune changes, suggesting that ecosystem-based patient classification in PDAC will facilitate the identification of candidates likely to benefit from immunotherapy. FUNDING: This work was supported by the National Key Research and Development Program of China, the Shanghai International Science and Technology Collaboration Program, the Shanghai Sailing Program, and the Key Laboratory of diagnosis and treatment of severe hepato-pancreatic diseases of Zhejiang Province.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Carcinoma Ductal Pancreático / Neoplasias Hepáticas Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Med Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Carcinoma Ductal Pancreático / Neoplasias Hepáticas Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Med Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos