neoplasm
• in a B16-mOVA tumor cell intravenous transplantation model, mice exhibit increased tumor volume, weight and growth compared to wild-type mice
• tumor growth is exacerbated during the subsequent MC38-mOVA challenge
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immune system
• IgG purified from OVA-immunized mice with MC38-mOVA induction shows less potent bone marrow derived macrophage activation and phagocytosis of antibody-targeted tumor cells
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• in an OVA antigen-based immunization model, mice show a decrease in OVA-specific IgG2c+ plasma cells in the bone marrow and spleen in the tumor microenvironment
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• in an ovalbumin (OVA) antigen-based immunization model, mice show lower percentage of OVA-specific IgG2c+ germinal center B cells in the spleen in the tumor microenvironment
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• in an ovalbumin (OVA) antigen-based immunization model, mice show a decrease in OVA-specific IgG2c+ memory B cells in the spleen and bone marrow, indicating a reduction of class-switched memory B cells in the tumor microenvironment
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• after immunization of OVA antigen combined with Th1-prone adjuvant, OVA-specific IgG2c antibody production is decreased in serum
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• IgG purified from OVA-immunized mice with MC38-mOVA induction shows less potent bone marrow derived macrophage activation and phagocytosis of antibody-targeted tumor cells
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mortality/aging
• in the B16-mOVA tumor cell intravenous transplantation model, mice exhibit reduced survival compared with wild-type mice
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cellular
• IgG purified from OVA-immunized mice with MC38-mOVA induction shows less potent bone marrow derived macrophage activation and phagocytosis of antibody-targeted tumor cells
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hematopoietic system
• IgG purified from OVA-immunized mice with MC38-mOVA induction shows less potent bone marrow derived macrophage activation and phagocytosis of antibody-targeted tumor cells
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• in an OVA antigen-based immunization model, mice show a decrease in OVA-specific IgG2c+ plasma cells in the bone marrow and spleen in the tumor microenvironment
|
• in an ovalbumin (OVA) antigen-based immunization model, mice show lower percentage of OVA-specific IgG2c+ germinal center B cells in the spleen in the tumor microenvironment
|
• in an ovalbumin (OVA) antigen-based immunization model, mice show a decrease in OVA-specific IgG2c+ memory B cells in the spleen and bone marrow, indicating a reduction of class-switched memory B cells in the tumor microenvironment
|
• after immunization of OVA antigen combined with Th1-prone adjuvant, OVA-specific IgG2c antibody production is decreased in serum
|
• IgG purified from OVA-immunized mice with MC38-mOVA induction shows less potent bone marrow derived macrophage activation and phagocytosis of antibody-targeted tumor cells
|