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Article: Single-cell mapping reveals several immune subsets associated with liver metastasis of pancreatic ductal adenocarcinoma

TitleSingle-cell mapping reveals several immune subsets associated with liver metastasis of pancreatic ductal adenocarcinoma
Authors
Keywordsmacrophage
metastasis
pancreatic ductal adenocarcinoma
T cell
Translation to humans
tumor microenvironment
Issue Date13-Oct-2023
PublisherCell Press
Citation
Med, 2023, v. 4, n. 10, p. 728-743.e7 How to Cite?
Abstract

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.


Persistent Identifierhttp://hdl.handle.net/10722/348618
ISSN
2023 SCImago Journal Rankings: 3.253

 

DC FieldValueLanguage
dc.contributor.authorZhang, Ze-
dc.contributor.authorZhu, Xiao Qiang-
dc.contributor.authorYang, Feng-
dc.contributor.authorLai, Nan Nan-
dc.contributor.authorZhu, Le-
dc.contributor.authorCole, Kathryn-
dc.contributor.authorHu, Bei Yuan-
dc.contributor.authorLi, Tian En-
dc.contributor.authorZhu, Ying-
dc.contributor.authorZhang, Lu Min-
dc.contributor.authorWang, Shun-
dc.contributor.authorZheng, Yan-
dc.contributor.authorMao, Huarong-
dc.contributor.authorZhao, Yue-
dc.contributor.authorBruns, Christiane-
dc.contributor.authorVago, Razi-
dc.contributor.authorTu, Bo-
dc.contributor.authorWong, Jason W.H.-
dc.contributor.authorFu, De Liang-
dc.contributor.authorQin, Lun Xiu-
dc.contributor.authorDong, Qiong Zhu-
dc.date.accessioned2024-10-11T00:30:51Z-
dc.date.available2024-10-11T00:30:51Z-
dc.date.issued2023-10-13-
dc.identifier.citationMed, 2023, v. 4, n. 10, p. 728-743.e7-
dc.identifier.issn2666-6359-
dc.identifier.urihttp://hdl.handle.net/10722/348618-
dc.description.abstract<p>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<sup>+</sup>PD-1<sup>+</sup>CD39<sup>+</sup> T cells with cytotoxic and exhausted functional status and an increased proportion of CD73<sup>+</sup> 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.<br></p>-
dc.languageeng-
dc.publisherCell Press-
dc.relation.ispartofMed-
dc.subjectmacrophage-
dc.subjectmetastasis-
dc.subjectpancreatic ductal adenocarcinoma-
dc.subjectT cell-
dc.subjectTranslation to humans-
dc.subjecttumor microenvironment-
dc.titleSingle-cell mapping reveals several immune subsets associated with liver metastasis of pancreatic ductal adenocarcinoma-
dc.typeArticle-
dc.identifier.doi10.1016/j.medj.2023.07.010-
dc.identifier.pmid37633269-
dc.identifier.scopuseid_2-s2.0-85173262781-
dc.identifier.volume4-
dc.identifier.issue10-
dc.identifier.spage728-
dc.identifier.epage743.e7-
dc.identifier.eissn2666-6340-
dc.identifier.issnl2666-6340-

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