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Synthetic DNA Delivery of an Engineered Arginase Enzyme Can Modulate Specific Immunity In Vivo

Arginase is a complex and unique enzyme that plays diverse roles in health and disease. By metabolizing arginine, it can shape the outcome of innate and adaptive immune responses. The immunomodulatory capabilities of arginase could potentially be applied for local immunosuppression or induction of i...

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Autores principales: Khoshnejad, Makan, Perales-Puchalt, Alfredo, Dia, Yaya, Xiao, Peng, Patel, Ami, Xu, Ziyang, Zhu, Xizhou, Yun, Kun, Baboo, Ishana, Qureshi, Rehman, Humeau, Laurent, Muthumani, Kar, Weiner, David B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7406982/
https://www.ncbi.nlm.nih.gov/pubmed/32802913
http://dx.doi.org/10.1016/j.omtm.2020.05.025
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author Khoshnejad, Makan
Perales-Puchalt, Alfredo
Dia, Yaya
Xiao, Peng
Patel, Ami
Xu, Ziyang
Zhu, Xizhou
Yun, Kun
Baboo, Ishana
Qureshi, Rehman
Humeau, Laurent
Muthumani, Kar
Weiner, David B.
author_facet Khoshnejad, Makan
Perales-Puchalt, Alfredo
Dia, Yaya
Xiao, Peng
Patel, Ami
Xu, Ziyang
Zhu, Xizhou
Yun, Kun
Baboo, Ishana
Qureshi, Rehman
Humeau, Laurent
Muthumani, Kar
Weiner, David B.
author_sort Khoshnejad, Makan
collection PubMed
description Arginase is a complex and unique enzyme that plays diverse roles in health and disease. By metabolizing arginine, it can shape the outcome of innate and adaptive immune responses. The immunomodulatory capabilities of arginase could potentially be applied for local immunosuppression or induction of immune tolerance. With the use of an enhanced DNA delivery approach, we designed and studied a DNA-encoded secretable arginase enzyme as a tool for immune modulation and evaluated its immunomodulatory function in vivo. Strong immunosuppression of cluster of differentiation 4 (CD4) and CD8 T cells, as well as macrophages and dendritic cells, was observed in vitro in the presence of an arginase-rich supernatant. To further evaluate the efficacy of DNA-encoded arginase on in vivo immunosuppression against an antigen, a cancer antigen vaccine model was used in the presence or absence of DNA-encoded arginase. Significant in vivo immunosuppression was observed in the presence of DNA-encoded arginase. The efficacy of this DNA-encoded arginase delivery was examined in a local, imiquimod-induced, psoriasis-like, skin-inflammation model. Pretreatment of animals with the synthetic DNA-encoded arginase led to significant decreases in skin acanthosis, proinflammatory cytokines, and costimulatory molecules in extracted macrophages and dendritic cells. These results draw attention to the potential of direct in vivo-delivered arginase to function as an immunomodulatory agent for treatment of local inflammation or autoimmune diseases.
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spelling pubmed-74069822020-08-14 Synthetic DNA Delivery of an Engineered Arginase Enzyme Can Modulate Specific Immunity In Vivo Khoshnejad, Makan Perales-Puchalt, Alfredo Dia, Yaya Xiao, Peng Patel, Ami Xu, Ziyang Zhu, Xizhou Yun, Kun Baboo, Ishana Qureshi, Rehman Humeau, Laurent Muthumani, Kar Weiner, David B. Mol Ther Methods Clin Dev Article Arginase is a complex and unique enzyme that plays diverse roles in health and disease. By metabolizing arginine, it can shape the outcome of innate and adaptive immune responses. The immunomodulatory capabilities of arginase could potentially be applied for local immunosuppression or induction of immune tolerance. With the use of an enhanced DNA delivery approach, we designed and studied a DNA-encoded secretable arginase enzyme as a tool for immune modulation and evaluated its immunomodulatory function in vivo. Strong immunosuppression of cluster of differentiation 4 (CD4) and CD8 T cells, as well as macrophages and dendritic cells, was observed in vitro in the presence of an arginase-rich supernatant. To further evaluate the efficacy of DNA-encoded arginase on in vivo immunosuppression against an antigen, a cancer antigen vaccine model was used in the presence or absence of DNA-encoded arginase. Significant in vivo immunosuppression was observed in the presence of DNA-encoded arginase. The efficacy of this DNA-encoded arginase delivery was examined in a local, imiquimod-induced, psoriasis-like, skin-inflammation model. Pretreatment of animals with the synthetic DNA-encoded arginase led to significant decreases in skin acanthosis, proinflammatory cytokines, and costimulatory molecules in extracted macrophages and dendritic cells. These results draw attention to the potential of direct in vivo-delivered arginase to function as an immunomodulatory agent for treatment of local inflammation or autoimmune diseases. American Society of Gene & Cell Therapy 2020-06-01 /pmc/articles/PMC7406982/ /pubmed/32802913 http://dx.doi.org/10.1016/j.omtm.2020.05.025 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Khoshnejad, Makan
Perales-Puchalt, Alfredo
Dia, Yaya
Xiao, Peng
Patel, Ami
Xu, Ziyang
Zhu, Xizhou
Yun, Kun
Baboo, Ishana
Qureshi, Rehman
Humeau, Laurent
Muthumani, Kar
Weiner, David B.
Synthetic DNA Delivery of an Engineered Arginase Enzyme Can Modulate Specific Immunity In Vivo
title Synthetic DNA Delivery of an Engineered Arginase Enzyme Can Modulate Specific Immunity In Vivo
title_full Synthetic DNA Delivery of an Engineered Arginase Enzyme Can Modulate Specific Immunity In Vivo
title_fullStr Synthetic DNA Delivery of an Engineered Arginase Enzyme Can Modulate Specific Immunity In Vivo
title_full_unstemmed Synthetic DNA Delivery of an Engineered Arginase Enzyme Can Modulate Specific Immunity In Vivo
title_short Synthetic DNA Delivery of an Engineered Arginase Enzyme Can Modulate Specific Immunity In Vivo
title_sort synthetic dna delivery of an engineered arginase enzyme can modulate specific immunity in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7406982/
https://www.ncbi.nlm.nih.gov/pubmed/32802913
http://dx.doi.org/10.1016/j.omtm.2020.05.025
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