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Expression of Arginase I in Myeloid Cells Limits Control of Residual Disease after Radiation Therapy of Tumors in Mice
by
Newell, Pippa
, Crittenden, Marka R.
, Young, Kristina
, Jackson, Andrew M.
, Savage, Talicia
, Cottam, Benjamin
, Baird, Jason
, Gough, Michael J.
, Rodriguez, Paulo C.
in
Activation
/ Adaptive control systems
/ Adaptive immunity
/ Adaptive Immunity - radiation effects
/ Animals
/ Arginase - genetics
/ Arginase - metabolism
/ Cancer
/ Cell Line, Tumor
/ Deletion
/ Dose Fractionation
/ Gene expression
/ Gene Expression Regulation, Neoplastic - radiation effects
/ Gene Knockout Techniques
/ Immune response
/ Macrophages
/ Macrophages - immunology
/ Macrophages - metabolism
/ Macrophages - radiation effects
/ Mice
/ Myeloid cells
/ Myeloid Cells - immunology
/ Myeloid Cells - metabolism
/ Myeloid Cells - radiation effects
/ MYELOID CELLS IN RADIATION-INDUCED IMMUNOMODULATION
/ Neoplasm, Residual
/ Pancreatic Neoplasms - immunology
/ Pancreatic Neoplasms - metabolism
/ Pancreatic Neoplasms - pathology
/ Pancreatic Neoplasms - radiotherapy
/ Phenotypes
/ Radiation therapy
/ Radiotherapy
/ REGULAR ARTICLE
/ Residual neoplasm
/ Strategy
/ T lymphocytes
/ Therapy
/ Tumors
2014
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Expression of Arginase I in Myeloid Cells Limits Control of Residual Disease after Radiation Therapy of Tumors in Mice
by
Newell, Pippa
, Crittenden, Marka R.
, Young, Kristina
, Jackson, Andrew M.
, Savage, Talicia
, Cottam, Benjamin
, Baird, Jason
, Gough, Michael J.
, Rodriguez, Paulo C.
in
Activation
/ Adaptive control systems
/ Adaptive immunity
/ Adaptive Immunity - radiation effects
/ Animals
/ Arginase - genetics
/ Arginase - metabolism
/ Cancer
/ Cell Line, Tumor
/ Deletion
/ Dose Fractionation
/ Gene expression
/ Gene Expression Regulation, Neoplastic - radiation effects
/ Gene Knockout Techniques
/ Immune response
/ Macrophages
/ Macrophages - immunology
/ Macrophages - metabolism
/ Macrophages - radiation effects
/ Mice
/ Myeloid cells
/ Myeloid Cells - immunology
/ Myeloid Cells - metabolism
/ Myeloid Cells - radiation effects
/ MYELOID CELLS IN RADIATION-INDUCED IMMUNOMODULATION
/ Neoplasm, Residual
/ Pancreatic Neoplasms - immunology
/ Pancreatic Neoplasms - metabolism
/ Pancreatic Neoplasms - pathology
/ Pancreatic Neoplasms - radiotherapy
/ Phenotypes
/ Radiation therapy
/ Radiotherapy
/ REGULAR ARTICLE
/ Residual neoplasm
/ Strategy
/ T lymphocytes
/ Therapy
/ Tumors
2014
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Expression of Arginase I in Myeloid Cells Limits Control of Residual Disease after Radiation Therapy of Tumors in Mice
by
Newell, Pippa
, Crittenden, Marka R.
, Young, Kristina
, Jackson, Andrew M.
, Savage, Talicia
, Cottam, Benjamin
, Baird, Jason
, Gough, Michael J.
, Rodriguez, Paulo C.
in
Activation
/ Adaptive control systems
/ Adaptive immunity
/ Adaptive Immunity - radiation effects
/ Animals
/ Arginase - genetics
/ Arginase - metabolism
/ Cancer
/ Cell Line, Tumor
/ Deletion
/ Dose Fractionation
/ Gene expression
/ Gene Expression Regulation, Neoplastic - radiation effects
/ Gene Knockout Techniques
/ Immune response
/ Macrophages
/ Macrophages - immunology
/ Macrophages - metabolism
/ Macrophages - radiation effects
/ Mice
/ Myeloid cells
/ Myeloid Cells - immunology
/ Myeloid Cells - metabolism
/ Myeloid Cells - radiation effects
/ MYELOID CELLS IN RADIATION-INDUCED IMMUNOMODULATION
/ Neoplasm, Residual
/ Pancreatic Neoplasms - immunology
/ Pancreatic Neoplasms - metabolism
/ Pancreatic Neoplasms - pathology
/ Pancreatic Neoplasms - radiotherapy
/ Phenotypes
/ Radiation therapy
/ Radiotherapy
/ REGULAR ARTICLE
/ Residual neoplasm
/ Strategy
/ T lymphocytes
/ Therapy
/ Tumors
2014
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Expression of Arginase I in Myeloid Cells Limits Control of Residual Disease after Radiation Therapy of Tumors in Mice
Journal Article
Expression of Arginase I in Myeloid Cells Limits Control of Residual Disease after Radiation Therapy of Tumors in Mice
2014
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Overview
An accumulating body of evidence demonstrates that radiation therapy can generate adaptive immune responses that contribute to tumor control. However, in the absence of additional immune therapy, the adaptive immune response is insufficient to prevent tumor recurrence or affect distant disease. It has been shown in multiple models that tumor-infiltrating myeloid cells exhibit alternative activation phenotypes and are able to suppress adaptive immune responses, and recent data suggests that the myeloid response in tumors treated with cytotoxic therapy limits tumor control. We hypothesized that tumor myeloid cells inhibit the adaptive immune response after radiation therapy through expression of the enzyme arginase I. Using a myeloid cell-specific deletion of arginase I in mice, we demonstrate an improved tumor control after radiation therapy. However, tumors still recurred despite the conditional knockdown of arginase I. Since multiple alternative factors may combine to inhibit adaptive immunity, we propose that targeting macrophage differentiation may be a more effective strategy than targeting individual suppressive pathways.
Publisher
The Radiation Research Society,Radiation Research Society,Allen Press Inc
Subject
/ Adaptive Immunity - radiation effects
/ Animals
/ Cancer
/ Deletion
/ Gene Expression Regulation, Neoplastic - radiation effects
/ Macrophages - radiation effects
/ Mice
/ Myeloid Cells - radiation effects
/ MYELOID CELLS IN RADIATION-INDUCED IMMUNOMODULATION
/ Pancreatic Neoplasms - immunology
/ Pancreatic Neoplasms - metabolism
/ Pancreatic Neoplasms - pathology
/ Pancreatic Neoplasms - radiotherapy
/ Strategy
/ Therapy
/ Tumors
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