hematopoietic system
• impaired Th17 cell differentiation as determined by decreased number of IL17+ CD4+ T cells following in vitro stimulation under Th17 polarizing conditions
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• reduced percentage of IL17+ CD4+ T cells following in vitro stimulation under Th17 polarizing conditions
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• fewer numbers of IFNG+ and IL17+ CD4+ T effector cells observed in brain following EAE induction as compared to controls and homozygous Socs1tm1.1Ayr mice
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• decreased numbers of CD4+ Foxp3+ T cells in thymus and spleen as compared to wild-type
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• reduced proliferation of splenic CD4+ T cells following restimulation with MOG35-55 peptide
• phenotype is less severe than in homozygous Socs1tm1.1Ayr mice
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immune system
• impaired Th17 cell differentiation as determined by decreased number of IL17+ CD4+ T cells following in vitro stimulation under Th17 polarizing conditions
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• reduced percentage of IL17+ CD4+ T cells following in vitro stimulation under Th17 polarizing conditions
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• fewer numbers of IFNG+ and IL17+ CD4+ T effector cells observed in brain following EAE induction as compared to controls and homozygous Socs1tm1.1Ayr mice
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• decreased numbers of CD4+ Foxp3+ T cells in thymus and spleen as compared to wild-type
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• reduced proliferation of splenic CD4+ T cells following restimulation with MOG35-55 peptide
• phenotype is less severe than in homozygous Socs1tm1.1Ayr mice
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• dendritic cells produce less of the pro-inflammatory cytokine IL6 following LPS stimulation than controls and homozygous Socs1tm1.1Ayr mice
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• attenuated EAE phenotype; phenotype is less severe than that observed in homozygous Socs1tm1.1Ayr mice
• most severe phenotype is observed in wild type mice
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