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

Authors :
Makan Khoshnejad
Alfredo Perales-Puchalt
Yaya Dia
Peng Xiao
Ami Patel
Ziyang Xu
Xizhou Zhu
Kun Yun
Ishana Baboo
Rehman Qureshi
Laurent Humeau
Kar Muthumani
David B. Weiner
Source :
Molecular Therapy: Methods & Clinical Development, Vol 18, Iss , Pp 652-663 (2020)
Publication Year :
2020
Publisher :
Elsevier, 2020.

Abstract

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.

Details

Language :
English
ISSN :
23290501
Volume :
18
Issue :
652-663
Database :
Directory of Open Access Journals
Journal :
Molecular Therapy: Methods & Clinical Development
Publication Type :
Academic Journal
Accession number :
edsdoj.4b6264ac10cc4e5597009cccad27ac16
Document Type :
article
Full Text :
https://doi.org/10.1016/j.omtm.2020.05.025