immune system
• polyclonal T cell proliferation (anti-CD3 mAb-induced) and antigen-specific T cell proliferation (KLH-induced) are reduced
• anti-CD3 mAb-induced lymph node T cell proliferation from unprimed mice is also reduced
• T cells from draining lymph nodes of KLH-immunized mice mixed with irradiated splenocytes (source of APCs) show a reduced proliferative capacity
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• percentage of CD44 high and CD62L low CD4+ cells is decreased by 24% and 14%, respectively, in the spleen
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• mutants show reduced delayed-type hypersensitivity response, with reduced KLH-specific swelling in both the ears and footpads, much milder dermal edema and inflammatory infiltrates than wild-type, and significant reduction in macrophage accumulation in footpads
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• T cells from KLH-immunized mice show a 76% reduction in IFN-gamma production when stimulated with anti-CD3 mAb and a 49% reduction when stimulated with KLH
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• T cells from KLH-immunized mice show a reduction in IL-2 production when stimulated with anti-CD3 mAb
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hematopoietic system
• polyclonal T cell proliferation (anti-CD3 mAb-induced) and antigen-specific T cell proliferation (KLH-induced) are reduced
• anti-CD3 mAb-induced lymph node T cell proliferation from unprimed mice is also reduced
• T cells from draining lymph nodes of KLH-immunized mice mixed with irradiated splenocytes (source of APCs) show a reduced proliferative capacity
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• percentage of CD44 high and CD62L low CD4+ cells is decreased by 24% and 14%, respectively, in the spleen
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cellular
• polyclonal T cell proliferation (anti-CD3 mAb-induced) and antigen-specific T cell proliferation (KLH-induced) are reduced
• anti-CD3 mAb-induced lymph node T cell proliferation from unprimed mice is also reduced
• T cells from draining lymph nodes of KLH-immunized mice mixed with irradiated splenocytes (source of APCs) show a reduced proliferative capacity
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