mortality/aging
• die within 3 to 4 days after HSV1 infection
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immune system
• marked reduction in IFN-alpha and IFN-beta in response to HSV1 infection
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• in L. monocytogenes-infected or c-di-GMP-treated mice
(J:168746)
• marked reduction in IFN-alpha and IFN-beta in response to HSV1 infection
(J:201167)
|
• 2'3'cGAMP fails to enhance the production of ovalbumin-specific antibodies on day 17 following injection with ovalbumin
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• lung fibroblasts transfected with interferon stimulatory DNA fail to produce any detectable level of IFN-beta
• induction of IFN-beta in lung fibroblasts infected with the DNA viruses; herpes simplex virus 1 (HSV1), vaccinia virus (VACV) and a mutant strain of HSV1called d109 is largely abolished
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• production of IFN-beta and TNF in bone marrow derived macrophages transfected with interferon stimulatory DNA or herring testis DNA are defective
• induction of IFN-beta in l bone marrow derived macrophages infected with VACV or HSV1 strains d109 or 7134 is largely abolished
• induction of IFN-beta in l bone marrow derived macrophages infected with HSV1 is severely but not completely blocked
|
• cultured conventional dendritic cells fail to induce IFN-alpha or IFN-beta following transfection with interferon stimulatory DNA or herring testis DNA
• cultured conventional dendritic cells fail to induce IFN-beta following infections with HSV1 strain d109 or VACV and induction by wild-type HSV1 is partially inhibited
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• induction of IFN-alpha and IFN-beta by interferon stimulatory DNA, poly[dA:dT], and genomic DNA from E. coli and Vibrio cholerae in the presence of liposome is abolished
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• L. monocytogenes-infected produce less IFN-beta compared with similarly treated wild-type mice
• macrophages exhibit a modest decrease in response to Sendai virus compared with wild-type cells
• however, L. monocytogenes-induced TNFalpha production is normal
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• marked reduction in IFN-alpha and IFN-beta in response to HSV1 infection
|
• die within 3 to 4 days after HSV1 infection
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homeostasis/metabolism
• marked reduction in IFN-alpha and IFN-beta in response to HSV1 infection
|
• in L. monocytogenes-infected or c-di-GMP-treated mice
(J:168746)
• marked reduction in IFN-alpha and IFN-beta in response to HSV1 infection
(J:201167)
|
hematopoietic system
• production of IFN-beta and TNF in bone marrow derived macrophages transfected with interferon stimulatory DNA or herring testis DNA are defective
• induction of IFN-beta in l bone marrow derived macrophages infected with VACV or HSV1 strains d109 or 7134 is largely abolished
• induction of IFN-beta in l bone marrow derived macrophages infected with HSV1 is severely but not completely blocked
|