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Encapsulated Checkpoint Blocker Before Chemotherapy: The Optimal Sequence of Anti-CTLA-4 and Doxil Combination Therapy

INTRODUCTION: Today, a new paradigm has emerged for cancer treatment introducing combination therapies. Doxil, a liposomal doxorubicin serving as a chemotherapeutic agent, is an effective immunogenic killer of cancer cells. Anti-CTLA-4 has been approved for the treatment of some cancers, including m...

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Autores principales: Alimohammadi, Reza, Alibeigi, Razieh, Nikpoor, Amin Reza, Chalbatani, Ghanbar Mahmoodi, Webster, Thomas J, Jaafari, Mahmoud Reza, Jalali, Seyed Amir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394514/
https://www.ncbi.nlm.nih.gov/pubmed/32801691
http://dx.doi.org/10.2147/IJN.S260760
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author Alimohammadi, Reza
Alibeigi, Razieh
Nikpoor, Amin Reza
Chalbatani, Ghanbar Mahmoodi
Webster, Thomas J
Jaafari, Mahmoud Reza
Jalali, Seyed Amir
author_facet Alimohammadi, Reza
Alibeigi, Razieh
Nikpoor, Amin Reza
Chalbatani, Ghanbar Mahmoodi
Webster, Thomas J
Jaafari, Mahmoud Reza
Jalali, Seyed Amir
author_sort Alimohammadi, Reza
collection PubMed
description INTRODUCTION: Today, a new paradigm has emerged for cancer treatment introducing combination therapies. Doxil, a liposomal doxorubicin serving as a chemotherapeutic agent, is an effective immunogenic killer of cancer cells. Anti-CTLA-4 has been approved for the treatment of some cancers, including melanoma, but side effects have limited its therapeutic potential. METHODS: In this study, two approaches were utilized to increase treatment efficiency and decrease the side effects of anti-CTLA-4, combining it with chemotherapy and encapsulation in a PEGylated liposome. A different sequence of anti-CTLA-4 and Doxil was assessed in combination therapy using non-liposomal and liposomal anti-CTLA-4. RESULTS: Our results showed that liposomal anti-CTLA-4 reduced the size of established tumors and increased survival in comparison with non-liposomal anti-CTLA-4 in a well-established B16 mouse melanoma model. In combination therapy with Doxil, only the administration of anti-CTLA-4 before Doxil showed synergism in both non-liposomal and liposomal form and increased the CD8(+)/regulatory T cell ratio. DISCUSSION: In summary, our results demonstrate the potential of utilizing a nanocarrier system for the delivery of checkpoint blockers, such as anti-CTLA-4 which further showed potential in a combination therapy, especially when administered before chemotherapy.
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spelling pubmed-73945142020-08-13 Encapsulated Checkpoint Blocker Before Chemotherapy: The Optimal Sequence of Anti-CTLA-4 and Doxil Combination Therapy Alimohammadi, Reza Alibeigi, Razieh Nikpoor, Amin Reza Chalbatani, Ghanbar Mahmoodi Webster, Thomas J Jaafari, Mahmoud Reza Jalali, Seyed Amir Int J Nanomedicine Original Research INTRODUCTION: Today, a new paradigm has emerged for cancer treatment introducing combination therapies. Doxil, a liposomal doxorubicin serving as a chemotherapeutic agent, is an effective immunogenic killer of cancer cells. Anti-CTLA-4 has been approved for the treatment of some cancers, including melanoma, but side effects have limited its therapeutic potential. METHODS: In this study, two approaches were utilized to increase treatment efficiency and decrease the side effects of anti-CTLA-4, combining it with chemotherapy and encapsulation in a PEGylated liposome. A different sequence of anti-CTLA-4 and Doxil was assessed in combination therapy using non-liposomal and liposomal anti-CTLA-4. RESULTS: Our results showed that liposomal anti-CTLA-4 reduced the size of established tumors and increased survival in comparison with non-liposomal anti-CTLA-4 in a well-established B16 mouse melanoma model. In combination therapy with Doxil, only the administration of anti-CTLA-4 before Doxil showed synergism in both non-liposomal and liposomal form and increased the CD8(+)/regulatory T cell ratio. DISCUSSION: In summary, our results demonstrate the potential of utilizing a nanocarrier system for the delivery of checkpoint blockers, such as anti-CTLA-4 which further showed potential in a combination therapy, especially when administered before chemotherapy. Dove 2020-07-27 /pmc/articles/PMC7394514/ /pubmed/32801691 http://dx.doi.org/10.2147/IJN.S260760 Text en © 2020 Alimohammadi et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Alimohammadi, Reza
Alibeigi, Razieh
Nikpoor, Amin Reza
Chalbatani, Ghanbar Mahmoodi
Webster, Thomas J
Jaafari, Mahmoud Reza
Jalali, Seyed Amir
Encapsulated Checkpoint Blocker Before Chemotherapy: The Optimal Sequence of Anti-CTLA-4 and Doxil Combination Therapy
title Encapsulated Checkpoint Blocker Before Chemotherapy: The Optimal Sequence of Anti-CTLA-4 and Doxil Combination Therapy
title_full Encapsulated Checkpoint Blocker Before Chemotherapy: The Optimal Sequence of Anti-CTLA-4 and Doxil Combination Therapy
title_fullStr Encapsulated Checkpoint Blocker Before Chemotherapy: The Optimal Sequence of Anti-CTLA-4 and Doxil Combination Therapy
title_full_unstemmed Encapsulated Checkpoint Blocker Before Chemotherapy: The Optimal Sequence of Anti-CTLA-4 and Doxil Combination Therapy
title_short Encapsulated Checkpoint Blocker Before Chemotherapy: The Optimal Sequence of Anti-CTLA-4 and Doxil Combination Therapy
title_sort encapsulated checkpoint blocker before chemotherapy: the optimal sequence of anti-ctla-4 and doxil combination therapy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394514/
https://www.ncbi.nlm.nih.gov/pubmed/32801691
http://dx.doi.org/10.2147/IJN.S260760
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