Guest guest Posted January 3, 2010 Report Share Posted January 3, 2010 Incredibly interesting http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2665180/?tool=pubmed .... The innate and adaptive responses to HIV and SIV infection in the CNS play a large role in the course of CNS disease, but are less well characterized than the responses found in the blood and lymphoid organs. Virus enters the brain within two weeks of infection, and if an effective systemic immune response occurs, becomes relatively quiescent until end-stage disease, when in a fraction of people and animals pronounced neurological symptoms can occur accompanied by encephalitisŠ ŠSince HIV/SIV in the brain is largely derived from macrophages, we examined whether the infectious phenotype of virions produced in macrophages might differ from those produced in T cells. Such virions showed no difference in genomic RNA/Gag or Env/Gag ratios, and sequence analysis revealed no mutations resulting from production in the different cell types. Infectivity assays, using a number of in vitro and in vivo derived targets, revealed a significantly higher infectivity of macrophage derived virions. Š.The 3 to 10 fold greater infectivity of macrophage derived virions, amplified over even a few rounds of viral replication, can result in an enormous increase in the spread of infection in the brain, where macrophages are the primary source and target for HIV infection. ALSO: ... Interestingly, our recent work in monkeys reveals that both plasma osteopontin, and one of its receptors on monocytes, CD44v6, are increased in animals developing SIV encephalitis, and that in HIV-infected people, osteopontin levels increase proportionally to the severity of CNS dysfunction. Has anyone looked into plasma osteopontin or CD44v6 levels in autism?? (I could not find any info/research out there). It would be highly interesting if results positive!! FINALLY: We have utilized a number of testing modalities, Š these indeed revealed that CNS ABNORMALITIES ARE COMMON IN OTHERWISE ASYMPTOMATIC SIV-infected rhesus monkeys. Š Interestingly, analysis of the circadian rhythms of body temperature and movement in monkeys that developed SIV encephalitis revealed impairments in circadian rhythms that preceded clinical symptoms Isn't 2-3 week period (at most) what people report re regression after vaccination, i.e. enough for the virus to enter the brain and spread there? Natasa Quote Link to comment Share on other sites More sharing options...
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