immune system
• with absence of Il4 and Il5, eosinophilia is completely blocked
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• mastocytosis is abolished compared to wild-type or triple mutants
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• no jejunal mast cell protease 1 is produced by mutants compared to wild-type or other allele combinations
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• Il-10 expression is reduced compared to Il5tm1Anjm mutants
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• mice show a switch to a Th1 response and Il12 production from a Th2 response
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• mutants fail to produce IgE, due to deletion of Il4
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• primary granuloma formation and volumes in lungs after infection are severely reduced (<10%) compared to wild-type
• secondary granuloma formation is essentially blocked
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• expulsion of worms is delayed by an order of magnitude vs triple mutants
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• compound quadruple mutants show ~1 order of magnitude greater delay in expulsion of worms from intestine (50% remain at day 60 after infection) than triple mutants (35 days)
• more worms remain at 40 days post infection than in triple Il4/Il5/Il13 mutants or wild-type
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digestive/alimentary system
• goblet cell hyperplasia is severely impaired after nematode infection with little increase in cell number observed even at 40 days post-infection
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hematopoietic system
• with absence of Il4 and Il5, eosinophilia is completely blocked
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• mastocytosis is abolished compared to wild-type or triple mutants
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• no jejunal mast cell protease 1 is produced by mutants compared to wild-type or other allele combinations
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• mutants fail to produce IgE, due to deletion of Il4
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homeostasis/metabolism
• Il-10 expression is reduced compared to Il5tm1Anjm mutants
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cellular
• goblet cell hyperplasia is severely impaired after nematode infection with little increase in cell number observed even at 40 days post-infection
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