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Robert L Elliott - One of the best experts on this subject based on the ideXlab platform.
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abstract 1664 inhibition of 4t1 mammary tumor growth in balb c mice by subcutaneous and Intraperitoneal Injection of a 4t1 whole cell vaccine containing il 2 and gm csf as adjuvants
Cancer Research, 2017Co-Authors: Jonathan F Head, Jeffrey T Phillips, Xianpeng Jiang, Robert L ElliottAbstract:Developing animal tumor models for human cancer vaccines creates a tool to investigate the mechanism of action, variations in formulation, dosing schedules, and combinations with other forms of cancer therapy. In this study we developed a mouse whole cell mammary cancer vaccine model with both subcutaneous and Intraperitoneal Injection of the vaccine. The vaccine, containing 4T1 mouse mammary cancer cells (1,000,000 cells), IL-2 (0.2 µg) and GM-CSF (0.1 µg) in a total volume of 150 µl, was injected either subcutaneously into the backs of BALB/c mice or Intraperitoneally. There were six Injections of the vaccine (weeks 1, 2, 3, 7, 11, 15) and one week after the last Injection 100,000 4T1 cells from cell culture in a volume of 100 µl were injected into the scapular region of the mice. At 22 days post 4T1 tumor transplantation there was a 37% inhibition of the growth of the 4T1 tumor in the mice receiving the subcutaneous Injection of the vaccine and a 42% inhibition of the growth of the 4T1 tumor in the mice receiving the Intraperitoneal Injection of the vaccine. The inhibition of 4T1 mammary tumor growth in this mouse model with subcutaneous Injection of a whole cell vaccine gives further support for the previously reported efficacy in a Phase 1/2 clinical trial of our therapeutic breast cancer vaccine containing autologous and allogeneic breast cancer cells in the adjuvant setting. The inhibition of 4T1 tumor growth with Intraperitoneal Injection suggests a delivery method that may be applicable to ovarian cancer and cancer patients with malignant ascites. Citation Format: Jonathan F. Head, Jeffrey T. Phillips, Xianpeng Jiang, Robert L. Elliott. Inhibition of 4T1 mammary tumor growth in BALB/c mice by subcutaneous and Intraperitoneal Injection of a 4T1 whole cell vaccine containing IL-2 and GM-CSF as adjuvants [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2017; 2017 Apr 1-5; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 1664. doi:10.1158/1538-7445.AM2017-1664
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Abstract 1664: Inhibition of 4T1 mammary tumor growth in BALB/c mice by subcutaneous and Intraperitoneal Injection of a 4T1 whole cell vaccine containing IL-2 and GM-CSF as adjuvants
Cancer Research, 2017Co-Authors: Jonathan F Head, Jeffrey T Phillips, Xianpeng Jiang, Robert L ElliottAbstract:Developing animal tumor models for human cancer vaccines creates a tool to investigate the mechanism of action, variations in formulation, dosing schedules, and combinations with other forms of cancer therapy. In this study we developed a mouse whole cell mammary cancer vaccine model with both subcutaneous and Intraperitoneal Injection of the vaccine. The vaccine, containing 4T1 mouse mammary cancer cells (1,000,000 cells), IL-2 (0.2 µg) and GM-CSF (0.1 µg) in a total volume of 150 µl, was injected either subcutaneously into the backs of BALB/c mice or Intraperitoneally. There were six Injections of the vaccine (weeks 1, 2, 3, 7, 11, 15) and one week after the last Injection 100,000 4T1 cells from cell culture in a volume of 100 µl were injected into the scapular region of the mice. At 22 days post 4T1 tumor transplantation there was a 37% inhibition of the growth of the 4T1 tumor in the mice receiving the subcutaneous Injection of the vaccine and a 42% inhibition of the growth of the 4T1 tumor in the mice receiving the Intraperitoneal Injection of the vaccine. The inhibition of 4T1 mammary tumor growth in this mouse model with subcutaneous Injection of a whole cell vaccine gives further support for the previously reported efficacy in a Phase 1/2 clinical trial of our therapeutic breast cancer vaccine containing autologous and allogeneic breast cancer cells in the adjuvant setting. The inhibition of 4T1 tumor growth with Intraperitoneal Injection suggests a delivery method that may be applicable to ovarian cancer and cancer patients with malignant ascites. Citation Format: Jonathan F. Head, Jeffrey T. Phillips, Xianpeng Jiang, Robert L. Elliott. Inhibition of 4T1 mammary tumor growth in BALB/c mice by subcutaneous and Intraperitoneal Injection of a 4T1 whole cell vaccine containing IL-2 and GM-CSF as adjuvants [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2017; 2017 Apr 1-5; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 1664. doi:10.1158/1538-7445.AM2017-1664
Jonathan F Head - One of the best experts on this subject based on the ideXlab platform.
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abstract 1664 inhibition of 4t1 mammary tumor growth in balb c mice by subcutaneous and Intraperitoneal Injection of a 4t1 whole cell vaccine containing il 2 and gm csf as adjuvants
Cancer Research, 2017Co-Authors: Jonathan F Head, Jeffrey T Phillips, Xianpeng Jiang, Robert L ElliottAbstract:Developing animal tumor models for human cancer vaccines creates a tool to investigate the mechanism of action, variations in formulation, dosing schedules, and combinations with other forms of cancer therapy. In this study we developed a mouse whole cell mammary cancer vaccine model with both subcutaneous and Intraperitoneal Injection of the vaccine. The vaccine, containing 4T1 mouse mammary cancer cells (1,000,000 cells), IL-2 (0.2 µg) and GM-CSF (0.1 µg) in a total volume of 150 µl, was injected either subcutaneously into the backs of BALB/c mice or Intraperitoneally. There were six Injections of the vaccine (weeks 1, 2, 3, 7, 11, 15) and one week after the last Injection 100,000 4T1 cells from cell culture in a volume of 100 µl were injected into the scapular region of the mice. At 22 days post 4T1 tumor transplantation there was a 37% inhibition of the growth of the 4T1 tumor in the mice receiving the subcutaneous Injection of the vaccine and a 42% inhibition of the growth of the 4T1 tumor in the mice receiving the Intraperitoneal Injection of the vaccine. The inhibition of 4T1 mammary tumor growth in this mouse model with subcutaneous Injection of a whole cell vaccine gives further support for the previously reported efficacy in a Phase 1/2 clinical trial of our therapeutic breast cancer vaccine containing autologous and allogeneic breast cancer cells in the adjuvant setting. The inhibition of 4T1 tumor growth with Intraperitoneal Injection suggests a delivery method that may be applicable to ovarian cancer and cancer patients with malignant ascites. Citation Format: Jonathan F. Head, Jeffrey T. Phillips, Xianpeng Jiang, Robert L. Elliott. Inhibition of 4T1 mammary tumor growth in BALB/c mice by subcutaneous and Intraperitoneal Injection of a 4T1 whole cell vaccine containing IL-2 and GM-CSF as adjuvants [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2017; 2017 Apr 1-5; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 1664. doi:10.1158/1538-7445.AM2017-1664
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Abstract 1664: Inhibition of 4T1 mammary tumor growth in BALB/c mice by subcutaneous and Intraperitoneal Injection of a 4T1 whole cell vaccine containing IL-2 and GM-CSF as adjuvants
Cancer Research, 2017Co-Authors: Jonathan F Head, Jeffrey T Phillips, Xianpeng Jiang, Robert L ElliottAbstract:Developing animal tumor models for human cancer vaccines creates a tool to investigate the mechanism of action, variations in formulation, dosing schedules, and combinations with other forms of cancer therapy. In this study we developed a mouse whole cell mammary cancer vaccine model with both subcutaneous and Intraperitoneal Injection of the vaccine. The vaccine, containing 4T1 mouse mammary cancer cells (1,000,000 cells), IL-2 (0.2 µg) and GM-CSF (0.1 µg) in a total volume of 150 µl, was injected either subcutaneously into the backs of BALB/c mice or Intraperitoneally. There were six Injections of the vaccine (weeks 1, 2, 3, 7, 11, 15) and one week after the last Injection 100,000 4T1 cells from cell culture in a volume of 100 µl were injected into the scapular region of the mice. At 22 days post 4T1 tumor transplantation there was a 37% inhibition of the growth of the 4T1 tumor in the mice receiving the subcutaneous Injection of the vaccine and a 42% inhibition of the growth of the 4T1 tumor in the mice receiving the Intraperitoneal Injection of the vaccine. The inhibition of 4T1 mammary tumor growth in this mouse model with subcutaneous Injection of a whole cell vaccine gives further support for the previously reported efficacy in a Phase 1/2 clinical trial of our therapeutic breast cancer vaccine containing autologous and allogeneic breast cancer cells in the adjuvant setting. The inhibition of 4T1 tumor growth with Intraperitoneal Injection suggests a delivery method that may be applicable to ovarian cancer and cancer patients with malignant ascites. Citation Format: Jonathan F. Head, Jeffrey T. Phillips, Xianpeng Jiang, Robert L. Elliott. Inhibition of 4T1 mammary tumor growth in BALB/c mice by subcutaneous and Intraperitoneal Injection of a 4T1 whole cell vaccine containing IL-2 and GM-CSF as adjuvants [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2017; 2017 Apr 1-5; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 1664. doi:10.1158/1538-7445.AM2017-1664
Hiroshi Kunugi - One of the best experts on this subject based on the ideXlab platform.
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A Single Intraperitoneal Injection of Endotoxin Changes Glial Cells in Rats as Revealed by Positron Emission Tomography Using [11C]PK11195.
Nuclear medicine and molecular imaging, 2018Co-Authors: Miho Ota, Jun Ogura, Shintaro Ogawa, Koichi Kato, Hiroshi Matsuda, Hiroshi KunugiAbstract:Intracranial administration of lipopolysaccharide (LPS) is known to elicit a rapid innate immune response, activate glial cells in the brain, and induce depression-like behavior. However, no study has focused on the changes in glial cells induced by Intraperitoneal Injection of LPS in vivo. Ten adult male Fischer F344 rats underwent [11C]PK11195 PET before and 2 days after Intraperitoneal Injection of LPS to evaluate the changes in glial cells. The difference in standardized uptake values (SUV) of [11C]PK11195 between before and after Injection was determined. There was a cluster of brain regions that showed significant reductions in SUV. This cluster included the bilateral striata and bilateral frontal regions, especially the somatosensory areas. Changes in activity of glial cells induced by the Intraperitoneal Injection of LPS were detected in vivo by [11C]PK11195 PET. Intraperitoneal Injection of LPS is known to induce depression, and further studies with [11C]PK11195 PET would clarify the relationships between neuroinflammation and depression.
Jeffrey T Phillips - One of the best experts on this subject based on the ideXlab platform.
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abstract 1664 inhibition of 4t1 mammary tumor growth in balb c mice by subcutaneous and Intraperitoneal Injection of a 4t1 whole cell vaccine containing il 2 and gm csf as adjuvants
Cancer Research, 2017Co-Authors: Jonathan F Head, Jeffrey T Phillips, Xianpeng Jiang, Robert L ElliottAbstract:Developing animal tumor models for human cancer vaccines creates a tool to investigate the mechanism of action, variations in formulation, dosing schedules, and combinations with other forms of cancer therapy. In this study we developed a mouse whole cell mammary cancer vaccine model with both subcutaneous and Intraperitoneal Injection of the vaccine. The vaccine, containing 4T1 mouse mammary cancer cells (1,000,000 cells), IL-2 (0.2 µg) and GM-CSF (0.1 µg) in a total volume of 150 µl, was injected either subcutaneously into the backs of BALB/c mice or Intraperitoneally. There were six Injections of the vaccine (weeks 1, 2, 3, 7, 11, 15) and one week after the last Injection 100,000 4T1 cells from cell culture in a volume of 100 µl were injected into the scapular region of the mice. At 22 days post 4T1 tumor transplantation there was a 37% inhibition of the growth of the 4T1 tumor in the mice receiving the subcutaneous Injection of the vaccine and a 42% inhibition of the growth of the 4T1 tumor in the mice receiving the Intraperitoneal Injection of the vaccine. The inhibition of 4T1 mammary tumor growth in this mouse model with subcutaneous Injection of a whole cell vaccine gives further support for the previously reported efficacy in a Phase 1/2 clinical trial of our therapeutic breast cancer vaccine containing autologous and allogeneic breast cancer cells in the adjuvant setting. The inhibition of 4T1 tumor growth with Intraperitoneal Injection suggests a delivery method that may be applicable to ovarian cancer and cancer patients with malignant ascites. Citation Format: Jonathan F. Head, Jeffrey T. Phillips, Xianpeng Jiang, Robert L. Elliott. Inhibition of 4T1 mammary tumor growth in BALB/c mice by subcutaneous and Intraperitoneal Injection of a 4T1 whole cell vaccine containing IL-2 and GM-CSF as adjuvants [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2017; 2017 Apr 1-5; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 1664. doi:10.1158/1538-7445.AM2017-1664
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Abstract 1664: Inhibition of 4T1 mammary tumor growth in BALB/c mice by subcutaneous and Intraperitoneal Injection of a 4T1 whole cell vaccine containing IL-2 and GM-CSF as adjuvants
Cancer Research, 2017Co-Authors: Jonathan F Head, Jeffrey T Phillips, Xianpeng Jiang, Robert L ElliottAbstract:Developing animal tumor models for human cancer vaccines creates a tool to investigate the mechanism of action, variations in formulation, dosing schedules, and combinations with other forms of cancer therapy. In this study we developed a mouse whole cell mammary cancer vaccine model with both subcutaneous and Intraperitoneal Injection of the vaccine. The vaccine, containing 4T1 mouse mammary cancer cells (1,000,000 cells), IL-2 (0.2 µg) and GM-CSF (0.1 µg) in a total volume of 150 µl, was injected either subcutaneously into the backs of BALB/c mice or Intraperitoneally. There were six Injections of the vaccine (weeks 1, 2, 3, 7, 11, 15) and one week after the last Injection 100,000 4T1 cells from cell culture in a volume of 100 µl were injected into the scapular region of the mice. At 22 days post 4T1 tumor transplantation there was a 37% inhibition of the growth of the 4T1 tumor in the mice receiving the subcutaneous Injection of the vaccine and a 42% inhibition of the growth of the 4T1 tumor in the mice receiving the Intraperitoneal Injection of the vaccine. The inhibition of 4T1 mammary tumor growth in this mouse model with subcutaneous Injection of a whole cell vaccine gives further support for the previously reported efficacy in a Phase 1/2 clinical trial of our therapeutic breast cancer vaccine containing autologous and allogeneic breast cancer cells in the adjuvant setting. The inhibition of 4T1 tumor growth with Intraperitoneal Injection suggests a delivery method that may be applicable to ovarian cancer and cancer patients with malignant ascites. Citation Format: Jonathan F. Head, Jeffrey T. Phillips, Xianpeng Jiang, Robert L. Elliott. Inhibition of 4T1 mammary tumor growth in BALB/c mice by subcutaneous and Intraperitoneal Injection of a 4T1 whole cell vaccine containing IL-2 and GM-CSF as adjuvants [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2017; 2017 Apr 1-5; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 1664. doi:10.1158/1538-7445.AM2017-1664
Xianpeng Jiang - One of the best experts on this subject based on the ideXlab platform.
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abstract 1664 inhibition of 4t1 mammary tumor growth in balb c mice by subcutaneous and Intraperitoneal Injection of a 4t1 whole cell vaccine containing il 2 and gm csf as adjuvants
Cancer Research, 2017Co-Authors: Jonathan F Head, Jeffrey T Phillips, Xianpeng Jiang, Robert L ElliottAbstract:Developing animal tumor models for human cancer vaccines creates a tool to investigate the mechanism of action, variations in formulation, dosing schedules, and combinations with other forms of cancer therapy. In this study we developed a mouse whole cell mammary cancer vaccine model with both subcutaneous and Intraperitoneal Injection of the vaccine. The vaccine, containing 4T1 mouse mammary cancer cells (1,000,000 cells), IL-2 (0.2 µg) and GM-CSF (0.1 µg) in a total volume of 150 µl, was injected either subcutaneously into the backs of BALB/c mice or Intraperitoneally. There were six Injections of the vaccine (weeks 1, 2, 3, 7, 11, 15) and one week after the last Injection 100,000 4T1 cells from cell culture in a volume of 100 µl were injected into the scapular region of the mice. At 22 days post 4T1 tumor transplantation there was a 37% inhibition of the growth of the 4T1 tumor in the mice receiving the subcutaneous Injection of the vaccine and a 42% inhibition of the growth of the 4T1 tumor in the mice receiving the Intraperitoneal Injection of the vaccine. The inhibition of 4T1 mammary tumor growth in this mouse model with subcutaneous Injection of a whole cell vaccine gives further support for the previously reported efficacy in a Phase 1/2 clinical trial of our therapeutic breast cancer vaccine containing autologous and allogeneic breast cancer cells in the adjuvant setting. The inhibition of 4T1 tumor growth with Intraperitoneal Injection suggests a delivery method that may be applicable to ovarian cancer and cancer patients with malignant ascites. Citation Format: Jonathan F. Head, Jeffrey T. Phillips, Xianpeng Jiang, Robert L. Elliott. Inhibition of 4T1 mammary tumor growth in BALB/c mice by subcutaneous and Intraperitoneal Injection of a 4T1 whole cell vaccine containing IL-2 and GM-CSF as adjuvants [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2017; 2017 Apr 1-5; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 1664. doi:10.1158/1538-7445.AM2017-1664
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Abstract 1664: Inhibition of 4T1 mammary tumor growth in BALB/c mice by subcutaneous and Intraperitoneal Injection of a 4T1 whole cell vaccine containing IL-2 and GM-CSF as adjuvants
Cancer Research, 2017Co-Authors: Jonathan F Head, Jeffrey T Phillips, Xianpeng Jiang, Robert L ElliottAbstract:Developing animal tumor models for human cancer vaccines creates a tool to investigate the mechanism of action, variations in formulation, dosing schedules, and combinations with other forms of cancer therapy. In this study we developed a mouse whole cell mammary cancer vaccine model with both subcutaneous and Intraperitoneal Injection of the vaccine. The vaccine, containing 4T1 mouse mammary cancer cells (1,000,000 cells), IL-2 (0.2 µg) and GM-CSF (0.1 µg) in a total volume of 150 µl, was injected either subcutaneously into the backs of BALB/c mice or Intraperitoneally. There were six Injections of the vaccine (weeks 1, 2, 3, 7, 11, 15) and one week after the last Injection 100,000 4T1 cells from cell culture in a volume of 100 µl were injected into the scapular region of the mice. At 22 days post 4T1 tumor transplantation there was a 37% inhibition of the growth of the 4T1 tumor in the mice receiving the subcutaneous Injection of the vaccine and a 42% inhibition of the growth of the 4T1 tumor in the mice receiving the Intraperitoneal Injection of the vaccine. The inhibition of 4T1 mammary tumor growth in this mouse model with subcutaneous Injection of a whole cell vaccine gives further support for the previously reported efficacy in a Phase 1/2 clinical trial of our therapeutic breast cancer vaccine containing autologous and allogeneic breast cancer cells in the adjuvant setting. The inhibition of 4T1 tumor growth with Intraperitoneal Injection suggests a delivery method that may be applicable to ovarian cancer and cancer patients with malignant ascites. Citation Format: Jonathan F. Head, Jeffrey T. Phillips, Xianpeng Jiang, Robert L. Elliott. Inhibition of 4T1 mammary tumor growth in BALB/c mice by subcutaneous and Intraperitoneal Injection of a 4T1 whole cell vaccine containing IL-2 and GM-CSF as adjuvants [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2017; 2017 Apr 1-5; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 1664. doi:10.1158/1538-7445.AM2017-1664