immune system
• nearly all CD4+ T cells in aged mice exhibit an activated phenotype unlike in Tg(TcrAND)53Hed mice
• however, lymph node T cells maintain a naive phenotype in young mice
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• CD4+ T cells exhibit increased primary and secondary antigen-specific proliferative responses compared to in Rag1tm1Mom/Rag1tm1Mom Tg(TcrAND)53Hed mice
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• in response to primary and secondary pigeon cytochrome c stimulation, the frequency of IL4-secreting T cells is increased compared to in Rag1tm1Mom/Rag1tm1Mom Tg(TcrAND)53Hed mice
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hematopoietic system
• nearly all CD4+ T cells in aged mice exhibit an activated phenotype unlike in Tg(TcrAND)53Hed mice
• however, lymph node T cells maintain a naive phenotype in young mice
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• CD4+ T cells exhibit increased primary and secondary antigen-specific proliferative responses compared to in Rag1tm1Mom/Rag1tm1Mom Tg(TcrAND)53Hed mice
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cellular
• CD4+ T cells exhibit increased primary and secondary antigen-specific proliferative responses compared to in Rag1tm1Mom/Rag1tm1Mom Tg(TcrAND)53Hed mice
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