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Towards efficient cancer immunotherapy: advances in developing artificial antigen-presenting cells

Active anti-cancer immune responses depend on efficient presentation of tumor antigens and co-stimulatory signals by antigen-presenting cells (APCs). Therapy with autologous natural APCs is costly and time-consuming and results in variable outcomes in clinical trials. Therefore, development of artif...

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Detalles Bibliográficos
Autores principales: Eggermont, Loek J., Paulis, Leonie E., Tel, Jurjen, Figdor, Carl G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science Publishers 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4154451/
https://www.ncbi.nlm.nih.gov/pubmed/24998519
http://dx.doi.org/10.1016/j.tibtech.2014.06.007
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author Eggermont, Loek J.
Paulis, Leonie E.
Tel, Jurjen
Figdor, Carl G.
author_facet Eggermont, Loek J.
Paulis, Leonie E.
Tel, Jurjen
Figdor, Carl G.
author_sort Eggermont, Loek J.
collection PubMed
description Active anti-cancer immune responses depend on efficient presentation of tumor antigens and co-stimulatory signals by antigen-presenting cells (APCs). Therapy with autologous natural APCs is costly and time-consuming and results in variable outcomes in clinical trials. Therefore, development of artificial APCs (aAPCs) has attracted significant interest as an alternative. We discuss the characteristics of various types of acellular aAPCs, and their clinical potential in cancer immunotherapy. The size, shape, and ligand mobility of aAPCs and their presentation of different immunological signals can all have significant effects on cytotoxic T cell activation. Novel optimized aAPCs, combining carefully tuned properties, may lead to efficient immunomodulation and improved clinical responses in cancer immunotherapy.
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spelling pubmed-41544512014-09-06 Towards efficient cancer immunotherapy: advances in developing artificial antigen-presenting cells Eggermont, Loek J. Paulis, Leonie E. Tel, Jurjen Figdor, Carl G. Trends Biotechnol Review Active anti-cancer immune responses depend on efficient presentation of tumor antigens and co-stimulatory signals by antigen-presenting cells (APCs). Therapy with autologous natural APCs is costly and time-consuming and results in variable outcomes in clinical trials. Therefore, development of artificial APCs (aAPCs) has attracted significant interest as an alternative. We discuss the characteristics of various types of acellular aAPCs, and their clinical potential in cancer immunotherapy. The size, shape, and ligand mobility of aAPCs and their presentation of different immunological signals can all have significant effects on cytotoxic T cell activation. Novel optimized aAPCs, combining carefully tuned properties, may lead to efficient immunomodulation and improved clinical responses in cancer immunotherapy. Elsevier Science Publishers 2014-09 /pmc/articles/PMC4154451/ /pubmed/24998519 http://dx.doi.org/10.1016/j.tibtech.2014.06.007 Text en © 2014 The Authors https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution 3.0 Unported License (https://creativecommons.org/licenses/by/3.0/) .
spellingShingle Review
Eggermont, Loek J.
Paulis, Leonie E.
Tel, Jurjen
Figdor, Carl G.
Towards efficient cancer immunotherapy: advances in developing artificial antigen-presenting cells
title Towards efficient cancer immunotherapy: advances in developing artificial antigen-presenting cells
title_full Towards efficient cancer immunotherapy: advances in developing artificial antigen-presenting cells
title_fullStr Towards efficient cancer immunotherapy: advances in developing artificial antigen-presenting cells
title_full_unstemmed Towards efficient cancer immunotherapy: advances in developing artificial antigen-presenting cells
title_short Towards efficient cancer immunotherapy: advances in developing artificial antigen-presenting cells
title_sort towards efficient cancer immunotherapy: advances in developing artificial antigen-presenting cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4154451/
https://www.ncbi.nlm.nih.gov/pubmed/24998519
http://dx.doi.org/10.1016/j.tibtech.2014.06.007
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