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PD-L1 Targeting Immune-Microbubble Complex Enhances Therapeutic Index in Murine Colon Cancer Models

Cancer immunotherapy has revolutionized the way different neoplasms are treated. Among the different variations of cancer immunotherapy, the checkpoint inhibitors targeting the programmed cell death protein 1 (PD-1)/programmed death-ligand 1 (PD-L1) axis have been validated and are currently used in...

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Detalles Bibliográficos
Autores principales: Kim, Daehyun, Lee, Seung Soo, Moon, Hyungwon, Park, So Yeon, Lee, Hak Jong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7822446/
https://www.ncbi.nlm.nih.gov/pubmed/33374574
http://dx.doi.org/10.3390/ph14010006
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author Kim, Daehyun
Lee, Seung Soo
Moon, Hyungwon
Park, So Yeon
Lee, Hak Jong
author_facet Kim, Daehyun
Lee, Seung Soo
Moon, Hyungwon
Park, So Yeon
Lee, Hak Jong
author_sort Kim, Daehyun
collection PubMed
description Cancer immunotherapy has revolutionized the way different neoplasms are treated. Among the different variations of cancer immunotherapy, the checkpoint inhibitors targeting the programmed cell death protein 1 (PD-1)/programmed death-ligand 1 (PD-L1) axis have been validated and are currently used in the clinics. Nevertheless, these therapeutic antibodies are associated with significant side effects and are known to induce immune-related toxicities. To address these issues, we have developed an immune-microbubble complex (IMC) which not only reduces the toxicities associated with the antibodies but also enhances the therapeutic efficacy when combined with focused ultrasound. The concept of IMCs could be applied to any type of antibody-based treatment regimens to maximize their therapeutic potential.
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spelling pubmed-78224462021-01-23 PD-L1 Targeting Immune-Microbubble Complex Enhances Therapeutic Index in Murine Colon Cancer Models Kim, Daehyun Lee, Seung Soo Moon, Hyungwon Park, So Yeon Lee, Hak Jong Pharmaceuticals (Basel) Article Cancer immunotherapy has revolutionized the way different neoplasms are treated. Among the different variations of cancer immunotherapy, the checkpoint inhibitors targeting the programmed cell death protein 1 (PD-1)/programmed death-ligand 1 (PD-L1) axis have been validated and are currently used in the clinics. Nevertheless, these therapeutic antibodies are associated with significant side effects and are known to induce immune-related toxicities. To address these issues, we have developed an immune-microbubble complex (IMC) which not only reduces the toxicities associated with the antibodies but also enhances the therapeutic efficacy when combined with focused ultrasound. The concept of IMCs could be applied to any type of antibody-based treatment regimens to maximize their therapeutic potential. MDPI 2020-12-23 /pmc/articles/PMC7822446/ /pubmed/33374574 http://dx.doi.org/10.3390/ph14010006 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, Daehyun
Lee, Seung Soo
Moon, Hyungwon
Park, So Yeon
Lee, Hak Jong
PD-L1 Targeting Immune-Microbubble Complex Enhances Therapeutic Index in Murine Colon Cancer Models
title PD-L1 Targeting Immune-Microbubble Complex Enhances Therapeutic Index in Murine Colon Cancer Models
title_full PD-L1 Targeting Immune-Microbubble Complex Enhances Therapeutic Index in Murine Colon Cancer Models
title_fullStr PD-L1 Targeting Immune-Microbubble Complex Enhances Therapeutic Index in Murine Colon Cancer Models
title_full_unstemmed PD-L1 Targeting Immune-Microbubble Complex Enhances Therapeutic Index in Murine Colon Cancer Models
title_short PD-L1 Targeting Immune-Microbubble Complex Enhances Therapeutic Index in Murine Colon Cancer Models
title_sort pd-l1 targeting immune-microbubble complex enhances therapeutic index in murine colon cancer models
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7822446/
https://www.ncbi.nlm.nih.gov/pubmed/33374574
http://dx.doi.org/10.3390/ph14010006
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