Guest guest Posted July 3, 2010 Report Share Posted July 3, 2010 this is about parasites,but interesting about how the immune system can change as the infection progresses.I read something on fungal infections that alsO pointed to immune system changes after 4 or5 days. I think I got it turned around on the mature and immature dc's. but they play a role in activating MHC, so I just think maybe there is a point where the immune system can be supressed somehow and MHC may not be a factor than. so it seems that if this is a possability, than if you dont think theres fungal infections or even bacterial infections going on with WDB exposures, maybe you wouldn't believe that the immune system can become suppressed.? I dont know, I'm just wondering if you can have a supressed immune system and possabily still have antigen presentation going on. I also fell that along with getting damaged tissues,infection becomes a more likely problem. than theres compliment,which I've read before, with fungal infection also may also change antigen presentation abilities. so I just dont know, but the possability is there. so this is kindof where I stand. I cant really be factual because it's been to long sence I had my brain tottally rapped around this and even than I had these questions. theres just to much to the immune system and alot of spectulation and not many clear cut answers. to top it off theres a somewhat different immune function to different sets of organs, the second brain and so on. the danger signal model made alot of things make more sence to me, but again, I haven't been in that kind of research mode for quite awhile as I have something else on my plate. but I just fell theres a good possability that if we have immune supression, it's not going to mater what bad genes we have. ps,you can get the full text by clicking on the pp number and than clicking on the pdf or html at the top of the page.through the second link http://www3.interscience.wiley.com/cgi-bin/fulltext/123345131/HTMLSTART http://www3.interscience.wiley.com/journal/123490544/abstract?CRETRY=1 & SRETRY=0 ------------------------------------- this was interesting on TH17 http://www3.interscience.wiley.com/cgi-bin/fulltext/121489807/HTMLSTART Studies on the role of IL-17-producing T cells in immunity to fungal infections have generated more conflicting findings. Clearance of the fungal pathogen Crypotococcus neoformans is delayed and survival reduced in IL-23p19-/- mice [92]. Similarly, IL-17AR-/- mice have decreased resistance to systemic challenge with C. albicans; higher fungal burden in the kidney and reduced survival in knockout mice were associated with reduced mobilization of peripheral neutrophils and their recruitment to the kidney [93]. However, there is also evidence that IL-23 and IL-17 may have a negative role in immunity to fungal infection. IL-23p19-/- mice were less susceptible to intragastric infection with C. albicans and intranasal infection with Aspergillus fumigatus and this was associated with enhanced IL-12 and IFN- production [94]. This study concluded that IL-23 and IL-17 impaired the anti-fungal immunity by suppressing Th1 responses and the fungicidal activity of neutrophils. Quote Link to comment Share on other sites More sharing options...
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