mortality/aging
|
• signs of scurfy disease are delayed and are first seen at 4 weeks of age, with mutants dying at about 6 weeks of age
|
immune system
|
• increase in the percentage of CD4-CD8+CD44+ and CD4-CD8+CD45RBdull T cells compared to homozygous CD4 mice at 15 days of age
• decrease in the percentage of CD4-CD8+ T cells in aged mutants compared with aged homozygous CD4 mice
|
|
• increased IgG in 35 day or older mutants, but not in 15 day old mutants
|
|
• increased IgM in 35 day or older mutants, but not in 15 day old mutants
|
|
• lymphoid organs in 15 day old mutants have typical scurfy lesions in T cell areas, but quiescent B cell areas
|
|
• lymph nodes are normal size at day 15 but are enlarged by day 35
|
|
• increased IL-4 production in response to Con A stimulation in aged (P45), but not young (P16) mice, compared to homozygous Cd4 mutant mice
|
|
• increased IL-6 production in response to Con A stimulation in aged (P45), but not young (P16) mice, compared to homozygous Cd4 mutant mice
|
|
• increased TNF-alpha production in response to Con A stimulation in aged (P45), but not young (P16) mice, compared to homozygous Cd4 mutant mice
|
hematopoietic system
|
• increase in the percentage of CD4-CD8+CD44+ and CD4-CD8+CD45RBdull T cells compared to homozygous CD4 mice at 15 days of age
• decrease in the percentage of CD4-CD8+ T cells in aged mutants compared with aged homozygous CD4 mice
|
|
• increased IgG in 35 day or older mutants, but not in 15 day old mutants
|
|
• increased IgM in 35 day or older mutants, but not in 15 day old mutants
|