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Pseudotime dynamics of T cells in pancreatic ductal adenocarcinoma inform distinct functional states within the regulatory and cytotoxic T cells

Pancreatic ductal adenocarcinoma (PDAC) is among the deadliest types of cancer and has a 5-year survival of less than 8% owing to its complex biology. As PDAC is refractory to immunotherapy, we need to understand the functional dynamics of T cells in the PDAC microenvironment to develop alternative...

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Autores principales: Jainarayanan, Ashwin, Mouroug-Anand, Nithishwer, Arbe-Barnes, Edward H., Bush, Adam J., Bashford-Rogers, Rachael, Frampton, Adam, Heij, Lara, Middleton, Mark, Dustin, Michael L., Abu-Shah, Enas, Sivakumar, Shivan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034436/
https://www.ncbi.nlm.nih.gov/pubmed/36968070
http://dx.doi.org/10.1016/j.isci.2023.106324
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author Jainarayanan, Ashwin
Mouroug-Anand, Nithishwer
Arbe-Barnes, Edward H.
Bush, Adam J.
Bashford-Rogers, Rachael
Frampton, Adam
Heij, Lara
Middleton, Mark
Dustin, Michael L.
Abu-Shah, Enas
Sivakumar, Shivan
author_facet Jainarayanan, Ashwin
Mouroug-Anand, Nithishwer
Arbe-Barnes, Edward H.
Bush, Adam J.
Bashford-Rogers, Rachael
Frampton, Adam
Heij, Lara
Middleton, Mark
Dustin, Michael L.
Abu-Shah, Enas
Sivakumar, Shivan
author_sort Jainarayanan, Ashwin
collection PubMed
description Pancreatic ductal adenocarcinoma (PDAC) is among the deadliest types of cancer and has a 5-year survival of less than 8% owing to its complex biology. As PDAC is refractory to immunotherapy, we need to understand the functional dynamics of T cells in the PDAC microenvironment to develop alternative therapeutic strategies. In this study, we performed RNA velocity-based pseudotime analysis on a scRNA-seq dataset from surgically resected human PDAC specimens to gain insight into temporal gene expression patterns that best characterize the cell fates. The tumor microenvironment was seen to encompass a range of terminal states for the T cell trajectories with suppressive and non-tumor-responsive T cells dominating them. However, the results also reveal the existence of a functional branch of the T cell population that was not transitioning to exhausted and senescent states. These findings reveal various microenvironmental signals driving T cell patterns which can be useful in identifying new therapeutic avenues.
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spelling pubmed-100344362023-03-24 Pseudotime dynamics of T cells in pancreatic ductal adenocarcinoma inform distinct functional states within the regulatory and cytotoxic T cells Jainarayanan, Ashwin Mouroug-Anand, Nithishwer Arbe-Barnes, Edward H. Bush, Adam J. Bashford-Rogers, Rachael Frampton, Adam Heij, Lara Middleton, Mark Dustin, Michael L. Abu-Shah, Enas Sivakumar, Shivan iScience Article Pancreatic ductal adenocarcinoma (PDAC) is among the deadliest types of cancer and has a 5-year survival of less than 8% owing to its complex biology. As PDAC is refractory to immunotherapy, we need to understand the functional dynamics of T cells in the PDAC microenvironment to develop alternative therapeutic strategies. In this study, we performed RNA velocity-based pseudotime analysis on a scRNA-seq dataset from surgically resected human PDAC specimens to gain insight into temporal gene expression patterns that best characterize the cell fates. The tumor microenvironment was seen to encompass a range of terminal states for the T cell trajectories with suppressive and non-tumor-responsive T cells dominating them. However, the results also reveal the existence of a functional branch of the T cell population that was not transitioning to exhausted and senescent states. These findings reveal various microenvironmental signals driving T cell patterns which can be useful in identifying new therapeutic avenues. Elsevier 2023-03-07 /pmc/articles/PMC10034436/ /pubmed/36968070 http://dx.doi.org/10.1016/j.isci.2023.106324 Text en Crown Copyright © 2023. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Jainarayanan, Ashwin
Mouroug-Anand, Nithishwer
Arbe-Barnes, Edward H.
Bush, Adam J.
Bashford-Rogers, Rachael
Frampton, Adam
Heij, Lara
Middleton, Mark
Dustin, Michael L.
Abu-Shah, Enas
Sivakumar, Shivan
Pseudotime dynamics of T cells in pancreatic ductal adenocarcinoma inform distinct functional states within the regulatory and cytotoxic T cells
title Pseudotime dynamics of T cells in pancreatic ductal adenocarcinoma inform distinct functional states within the regulatory and cytotoxic T cells
title_full Pseudotime dynamics of T cells in pancreatic ductal adenocarcinoma inform distinct functional states within the regulatory and cytotoxic T cells
title_fullStr Pseudotime dynamics of T cells in pancreatic ductal adenocarcinoma inform distinct functional states within the regulatory and cytotoxic T cells
title_full_unstemmed Pseudotime dynamics of T cells in pancreatic ductal adenocarcinoma inform distinct functional states within the regulatory and cytotoxic T cells
title_short Pseudotime dynamics of T cells in pancreatic ductal adenocarcinoma inform distinct functional states within the regulatory and cytotoxic T cells
title_sort pseudotime dynamics of t cells in pancreatic ductal adenocarcinoma inform distinct functional states within the regulatory and cytotoxic t cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034436/
https://www.ncbi.nlm.nih.gov/pubmed/36968070
http://dx.doi.org/10.1016/j.isci.2023.106324
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