mortality/aging
• Background Sensitivity: mice die between 3 to 5 weeks of age
• can be prevented with adoptive transfer at birth of 3 x 104 CD25-positive CD4 T cells from wild-type mice
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immune system
• cause of death at 3 to 5 weeks of age
• can be prevented with adoptive transfer at birth of 3 x 104 CD25-positive CD4 T cells from wild-type mice
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• expected deletion occurs of T cells that recognize BALB/c specific superantigens, indicating the autoimmunity associated with this mouse strain is unlikely to be a failure to eliminate self-reactive T cells
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• number is reduced by a third upon transfer of 3 x 104 CD25-positive CD4 T cells from wild-type mice
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• percentage of CD4 and CD8 T cells that express high levels of activation markers is increased
• T cells are hyporesponsive to inflammatory cytokines as measured by in vitro proliferation assays
• expression of activation markers is normalized upon transfer of 3 x 104 CD25-positive CD4 T cells from wild-type mice
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• by 3 to 5 weeks of age
• can be prevented with adoptive transfer at birth of 3 x 104 CD25-positive CD4 T cells from wild-type mice
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• by 3 to 5 weeks of age
• can be prevented with adoptive transfer at birth of 3 x 104 CD25-positive CD4 T cells from wild-type mice
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• extension of marginal zones found in the spleen
• can be prevented with adoptive transfer at birth of 3 x 104 CD25-positive CD4 T cells from wild-type mice
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• increase in size
• can be prevented with adoptive transfer at birth of 3 x 104 CD25-positive CD4 T cells from wild-type mice
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• by 3 to 5 weeks of age
• can be prevented with adoptive transfer at birth of 3 x 104 CD25-positive CD4 T cells from wild-type mice
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• by 3 to 5 weeks of age
• can be prevented with adoptive transfer at birth of 3 x 104 CD25-positive CD4 T cells from wild-type mice
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• large atypical lymphocytes are observed in the liver
• no inflammation is observed in mice that receive transfer of 3 x 104 wild-type CD25-positive CD4 T
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liver/biliary system
• large atypical lymphocytes are observed in the liver
• no inflammation is observed in mice that receive transfer of 3 x 104 wild-type CD25-positive CD4 T
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hematopoietic system
• by 3 to 5 weeks of age
• can be prevented with adoptive transfer at birth of 3 x 104 CD25-positive CD4 T cells from wild-type mice
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• cause of death at 3 to 5 weeks of age
• can be prevented with adoptive transfer at birth of 3 x 104 CD25-positive CD4 T cells from wild-type mice
|
• expected deletion occurs of T cells that recognize BALB/c specific superantigens, indicating the autoimmunity associated with this mouse strain is unlikely to be a failure to eliminate self-reactive T cells
|
• number is reduced by a third upon transfer of 3 x 104 CD25-positive CD4 T cells from wild-type mice
|
• extension of marginal zones found in the spleen
• can be prevented with adoptive transfer at birth of 3 x 104 CD25-positive CD4 T cells from wild-type mice
|
• increase in size
• can be prevented with adoptive transfer at birth of 3 x 104 CD25-positive CD4 T cells from wild-type mice
|
• percentage of CD4 and CD8 T cells that express high levels of activation markers is increased
• T cells are hyporesponsive to inflammatory cytokines as measured by in vitro proliferation assays
• expression of activation markers is normalized upon transfer of 3 x 104 CD25-positive CD4 T cells from wild-type mice
|
• by 3 to 5 weeks of age
• can be prevented with adoptive transfer at birth of 3 x 104 CD25-positive CD4 T cells from wild-type mice
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growth/size/body
• by 3 to 5 weeks of age
• can be prevented with adoptive transfer at birth of 3 x 104 CD25-positive CD4 T cells from wild-type mice
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cellular
• by 3 to 5 weeks of age
• can be prevented with adoptive transfer at birth of 3 x 104 CD25-positive CD4 T cells from wild-type mice
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