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Innate immunity in pancreatic cancer: Lineage tracing and function

Increasingly, patients with gastrointestinal tumors can benefit from immunotherapy, but not patients with pancreatic cancer. While this lack of benefit has been attributed to lower T-cell infiltration in pancreatic cancer, other studies have demonstrated the presence of numerous T cells in pancreati...

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Detalles Bibliográficos
Autores principales: Ye, Longyun, Shi, Saimeng, Chen, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884680/
https://www.ncbi.nlm.nih.gov/pubmed/36726981
http://dx.doi.org/10.3389/fimmu.2022.1081919
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author Ye, Longyun
Shi, Saimeng
Chen, Wei
author_facet Ye, Longyun
Shi, Saimeng
Chen, Wei
author_sort Ye, Longyun
collection PubMed
description Increasingly, patients with gastrointestinal tumors can benefit from immunotherapy, but not patients with pancreatic cancer. While this lack of benefit has been attributed to lower T-cell infiltration in pancreatic cancer, other studies have demonstrated the presence of numerous T cells in pancreatic cancer, suggesting another mechanism for the poor efficacy of immunotherapy. Single-cell RNA sequencing studies on the pancreatic cancer immune microenvironment have demonstrated the predominance of innate immune cells (e.g., macrophages, dendritic cells, mast cells, and innate immune lymphoid cells). Therefore, in-depth research on the source and function of innate immune lymphocytes in pancreatic cancer could guide pancreatic cancer immunotherapy.
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spelling pubmed-98846802023-01-31 Innate immunity in pancreatic cancer: Lineage tracing and function Ye, Longyun Shi, Saimeng Chen, Wei Front Immunol Immunology Increasingly, patients with gastrointestinal tumors can benefit from immunotherapy, but not patients with pancreatic cancer. While this lack of benefit has been attributed to lower T-cell infiltration in pancreatic cancer, other studies have demonstrated the presence of numerous T cells in pancreatic cancer, suggesting another mechanism for the poor efficacy of immunotherapy. Single-cell RNA sequencing studies on the pancreatic cancer immune microenvironment have demonstrated the predominance of innate immune cells (e.g., macrophages, dendritic cells, mast cells, and innate immune lymphoid cells). Therefore, in-depth research on the source and function of innate immune lymphocytes in pancreatic cancer could guide pancreatic cancer immunotherapy. Frontiers Media S.A. 2023-01-16 /pmc/articles/PMC9884680/ /pubmed/36726981 http://dx.doi.org/10.3389/fimmu.2022.1081919 Text en Copyright © 2023 Ye, Shi and Chen https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Ye, Longyun
Shi, Saimeng
Chen, Wei
Innate immunity in pancreatic cancer: Lineage tracing and function
title Innate immunity in pancreatic cancer: Lineage tracing and function
title_full Innate immunity in pancreatic cancer: Lineage tracing and function
title_fullStr Innate immunity in pancreatic cancer: Lineage tracing and function
title_full_unstemmed Innate immunity in pancreatic cancer: Lineage tracing and function
title_short Innate immunity in pancreatic cancer: Lineage tracing and function
title_sort innate immunity in pancreatic cancer: lineage tracing and function
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884680/
https://www.ncbi.nlm.nih.gov/pubmed/36726981
http://dx.doi.org/10.3389/fimmu.2022.1081919
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