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Bose N, Chan A, Guerrero F, Maristany C, Qui X, Walsh R, Ertelt K, Jonas A, Gorden K, Dudney C, Wurst L, Danielson M, Elmasry N, Magee A, Patchen M, Vasilakos J (2013) Binding of soluble yeast beta-glucan to human neutrophils and monocytes is complement-dependent. Front Immunol 4:230
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Jonas A, Qiu X, Chan A, McMurray D, Bose N (2015) Imprime PGG, a yeast beta-glucan immunomodulator, can engage Fc gamma receptor (FcgR) in addition to complement receptor 3 (CR3) on human neutrophils and monocytes (abstract). Keystone Symposium on Tumor Immunology, Multidisciplinary Science Driving Combination Therapy, Banff, Alberta
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Bose N, Antonysamy M, Patchen M, Lowe J, Mattson P, Gargano M, Gordon K, Leonardo S, Walsh R, Qui X, McMurry D, Chan A, Jonas A, Huhn R, Thomas M, Sadjadian P, Schneller F (2014) Endogenous anti-beta-glucan antibodies as a potential predictive biomarker for clinical resposne to imprime PGG immunotherapy in non-small cell lung cancer (NSCLC) patients (abstract). J Clin Oncol 13(15S):3045
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Imprime PGG treatment enhances antibody-dependent cellular phagocytosis (ADCP) of tumor cells by monocyte-derived macrophages abstract
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Translating Science into Survival, New York, NY
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Imprime PGG, a yeast beta glucan immunomodulator, has the potential to repolarize human monocyte-derived M2 macrophages to M1 phenotype (abstract)
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Chan A, Qiu X, Bykowski Jonas A, Patchen M, Bose N (2014) Imprime PGG, a yeast beta glucan immunomodulator, has the potential to repolarize human monocyte-derived M2 macrophages to M1 phenotype (abstract). J Immunother Cancer 2(Suppl 3):P191
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Imprime PGG modulates the function of monocyte-derived M2 macrophages and dendritic cells to drive T cell expansion (abstract)
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Imprime PGG decreases regulatory T cell suppression and enhances T cell proliferation and differentiation revealing additional mechanisms for its anti-tumor activity (abstract)
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Symposia on Cancer Research: Emerging Concepts in Host Response to Cancer, Houston, TX
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Bose N, Fulton R, Chan A, Leonardo S, Fraser K, Jonas A, Ottoson N, Qiu X, Gorden K, Graff J (2015a) Imprime PGG, a yeast-derived Pathogen-Associated Molecular Pattern (PAMP), drives a coordinated anti-cancer immune attack (abstract). Symposia on Cancer Research: Emerging Concepts in Host Response to Cancer, Houston, TX
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Bose N, Chan A, Jonas A, Qiu X, Ottoson N, Kangas T, Graff J (2015b) Imprime PGG treatment elicits a coordinated antitumor immune response that triggers enhanced expression of PD-L1 on tumor cells as well as monocyte-derived macrophages and dendritic cells. Cancer Res 75 (Suppl 15):LB-228
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Imprime PGG a soluble beta-glucan, binds to and activate dendritic cells resulting in enhanced T cell priming, expansion, and cytokine production abstract
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Tamayo M, Cornelio G, Bautista J (2010) Safety, pharmacokinetics (PK), and efficacy of imprime PGG plus cetuximab (cetux) with and without irinotecan (irino) in advanced metastatic colorectal cancer (mCRC) patients (abstract). Ann Oncol 21(Suppl 8):4584
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