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Insights into CD47/SIRPα axis-targeting tumor immunotherapy

During the last decade, inhibitors targeting immune checkpoint programmed death ligand 1/PD-1 and cytotoxic T-lymphocyte-associated protein 4 have been one of the most significant advances for cancer therapy in clinic. However, most of these therapies focused on stimulating the adaptive immune syste...

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Detalles Bibliográficos
Autores principales: Zhang, Xuyao, Fan, Jiajun, Ju, Dianwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157794/
https://www.ncbi.nlm.nih.gov/pubmed/34056543
http://dx.doi.org/10.1093/abt/tby006
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author Zhang, Xuyao
Fan, Jiajun
Ju, Dianwen
author_facet Zhang, Xuyao
Fan, Jiajun
Ju, Dianwen
author_sort Zhang, Xuyao
collection PubMed
description During the last decade, inhibitors targeting immune checkpoint programmed death ligand 1/PD-1 and cytotoxic T-lymphocyte-associated protein 4 have been one of the most significant advances for cancer therapy in clinic. However, most of these therapies focused on stimulating the adaptive immune system-mediated elimination of tumor. Recent studies indicated that CD47/Signal-regulatory protein alpha (SIRPα), an innate anti-phagocytic axis between cancer cells and macrophages, could be a promising therapeutic target. Here, we review the current knowledge about developing CD47/SIRPα checkpoint inhibitors, avoiding potential side effect and designing optimal combination therapies, and highlight the key points for future clinical applications of CD47/SIRPα axis-targeted tumor immunotherapy.
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spelling pubmed-81577942021-05-28 Insights into CD47/SIRPα axis-targeting tumor immunotherapy Zhang, Xuyao Fan, Jiajun Ju, Dianwen Antib Ther Review During the last decade, inhibitors targeting immune checkpoint programmed death ligand 1/PD-1 and cytotoxic T-lymphocyte-associated protein 4 have been one of the most significant advances for cancer therapy in clinic. However, most of these therapies focused on stimulating the adaptive immune system-mediated elimination of tumor. Recent studies indicated that CD47/Signal-regulatory protein alpha (SIRPα), an innate anti-phagocytic axis between cancer cells and macrophages, could be a promising therapeutic target. Here, we review the current knowledge about developing CD47/SIRPα checkpoint inhibitors, avoiding potential side effect and designing optimal combination therapies, and highlight the key points for future clinical applications of CD47/SIRPα axis-targeted tumor immunotherapy. Oxford University Press 2018-08-28 /pmc/articles/PMC8157794/ /pubmed/34056543 http://dx.doi.org/10.1093/abt/tby006 Text en © The Author(s) (2018). Published by Oxford University Press on behalf of Antibody Therapeutics. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Review
Zhang, Xuyao
Fan, Jiajun
Ju, Dianwen
Insights into CD47/SIRPα axis-targeting tumor immunotherapy
title Insights into CD47/SIRPα axis-targeting tumor immunotherapy
title_full Insights into CD47/SIRPα axis-targeting tumor immunotherapy
title_fullStr Insights into CD47/SIRPα axis-targeting tumor immunotherapy
title_full_unstemmed Insights into CD47/SIRPα axis-targeting tumor immunotherapy
title_short Insights into CD47/SIRPα axis-targeting tumor immunotherapy
title_sort insights into cd47/sirpα axis-targeting tumor immunotherapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157794/
https://www.ncbi.nlm.nih.gov/pubmed/34056543
http://dx.doi.org/10.1093/abt/tby006
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