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Nano-enabled pancreas cancer immunotherapy using immunogenic cell death and reversing immunosuppression.


ABSTRACT: While chemotherapy delivery by nanocarriers has modestly improved the survival prospects of pancreatic ductal adenocarcinoma (PDAC), additional engagement of the immune response could be game changing. We demonstrate a nano-enabled approach for accomplishing robust anti-PDAC immunity in syngeneic mice through the induction of immunogenic cell death (ICD) as well as interfering in the immunosuppressive indoleamine 2,3-dioxygenase (IDO) pathway. This is accomplished by conjugating the IDO inhibitor, indoximod (IND), to a phospholipid that allows prodrug self-assembly into nanovesicles or incorporation into a lipid bilayer that encapsulates mesoporous silica nanoparticles (MSNP). The porous MSNP interior allows contemporaneous delivery of the ICD-inducing chemotherapeutic agent, oxaliplatin (OX). The nanovesicles plus free OX or OX/IND-MSNP induce effective innate and adaptive anti-PDAC immunity when used in a vaccination approach, direct tumor injection or intravenous biodistribution to an orthotopic PDAC site. Significant tumor reduction or eradication is accomplishable by recruiting cytotoxic T lymphocytes, concomitant with downregulation of Foxp3+ T cells.

SUBMITTER: Lu J 

PROVIDER: S-EPMC5703845 | biostudies-other | 2017 Nov

REPOSITORIES: biostudies-other

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Nano-enabled pancreas cancer immunotherapy using immunogenic cell death and reversing immunosuppression.

Lu Jianqin J   Liu Xiangsheng X   Liao Yu-Pei YP   Salazar Felix F   Sun Bingbing B   Jiang Wen W   Chang Chong Hyun CH   Jiang Jinhong J   Wang Xiang X   Wu Anna M AM   Meng Huan H   Nel Andre E AE  

Nature communications 20171127 1


While chemotherapy delivery by nanocarriers has modestly improved the survival prospects of pancreatic ductal adenocarcinoma (PDAC), additional engagement of the immune response could be game changing. We demonstrate a nano-enabled approach for accomplishing robust anti-PDAC immunity in syngeneic mice through the induction of immunogenic cell death (ICD) as well as interfering in the immunosuppressive indoleamine 2,3-dioxygenase (IDO) pathway. This is accomplished by conjugating the IDO inhibito  ...[more]

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