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A roadmap for translational cancer glycoimmunology at single cell resolution

Cancer cells can evade immune responses by exploiting inhibitory immune checkpoints. Immune checkpoint inhibitor (ICI) therapies based on anti-CTLA-4 and anti-PD-1/PD-L1 antibodies have been extensively explored over the recent years to unleash otherwise compromised anti-cancer immune responses. How...

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Autores principales: Peixoto, Andreia, Miranda, Andreia, Santos, Lúcio Lara, Ferreira, José Alexandre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9013178/
https://www.ncbi.nlm.nih.gov/pubmed/35428302
http://dx.doi.org/10.1186/s13046-022-02335-z
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author Peixoto, Andreia
Miranda, Andreia
Santos, Lúcio Lara
Ferreira, José Alexandre
author_facet Peixoto, Andreia
Miranda, Andreia
Santos, Lúcio Lara
Ferreira, José Alexandre
author_sort Peixoto, Andreia
collection PubMed
description Cancer cells can evade immune responses by exploiting inhibitory immune checkpoints. Immune checkpoint inhibitor (ICI) therapies based on anti-CTLA-4 and anti-PD-1/PD-L1 antibodies have been extensively explored over the recent years to unleash otherwise compromised anti-cancer immune responses. However, it is also well established that immune suppression is a multifactorial process involving an intricate crosstalk between cancer cells and the immune systems. The cancer glycome is emerging as a relevant source of immune checkpoints governing immunosuppressive behaviour in immune cells, paving an avenue for novel immunotherapeutic options. This review addresses the current state-of-the-art concerning the role played by glycans controlling innate and adaptive immune responses, while shedding light on available experimental models for glycoimmunology. We also emphasize the tremendous progress observed in the development of humanized models for immunology, the paramount contribution of advances in high-throughput single-cell analysis in this context, and the importance of including predictive machine learning algorithms in translational research. This may constitute an important roadmap for glycoimmunology, supporting careful adoption of models foreseeing clinical translation of fundamental glycobiology knowledge towards next generation immunotherapies.
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spelling pubmed-90131782022-04-17 A roadmap for translational cancer glycoimmunology at single cell resolution Peixoto, Andreia Miranda, Andreia Santos, Lúcio Lara Ferreira, José Alexandre J Exp Clin Cancer Res Review Cancer cells can evade immune responses by exploiting inhibitory immune checkpoints. Immune checkpoint inhibitor (ICI) therapies based on anti-CTLA-4 and anti-PD-1/PD-L1 antibodies have been extensively explored over the recent years to unleash otherwise compromised anti-cancer immune responses. However, it is also well established that immune suppression is a multifactorial process involving an intricate crosstalk between cancer cells and the immune systems. The cancer glycome is emerging as a relevant source of immune checkpoints governing immunosuppressive behaviour in immune cells, paving an avenue for novel immunotherapeutic options. This review addresses the current state-of-the-art concerning the role played by glycans controlling innate and adaptive immune responses, while shedding light on available experimental models for glycoimmunology. We also emphasize the tremendous progress observed in the development of humanized models for immunology, the paramount contribution of advances in high-throughput single-cell analysis in this context, and the importance of including predictive machine learning algorithms in translational research. This may constitute an important roadmap for glycoimmunology, supporting careful adoption of models foreseeing clinical translation of fundamental glycobiology knowledge towards next generation immunotherapies. BioMed Central 2022-04-15 /pmc/articles/PMC9013178/ /pubmed/35428302 http://dx.doi.org/10.1186/s13046-022-02335-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Peixoto, Andreia
Miranda, Andreia
Santos, Lúcio Lara
Ferreira, José Alexandre
A roadmap for translational cancer glycoimmunology at single cell resolution
title A roadmap for translational cancer glycoimmunology at single cell resolution
title_full A roadmap for translational cancer glycoimmunology at single cell resolution
title_fullStr A roadmap for translational cancer glycoimmunology at single cell resolution
title_full_unstemmed A roadmap for translational cancer glycoimmunology at single cell resolution
title_short A roadmap for translational cancer glycoimmunology at single cell resolution
title_sort roadmap for translational cancer glycoimmunology at single cell resolution
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9013178/
https://www.ncbi.nlm.nih.gov/pubmed/35428302
http://dx.doi.org/10.1186/s13046-022-02335-z
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