Guest guest Posted October 16, 2005 Report Share Posted October 16, 2005 This stuff is SO freakin abstruse. Not sure anyone wants a look at this one... basic story is they created AI disease in mice by injecting T-cell lines. (Clever controls they used established very clearly that the disease was AI.) http://www.pubmedcentral.gov/articlerender.fcgi? tool=pubmed & pubmedid=10841661 Sounds impressive, but check the fine print on the mice: " We have previously revealed that RAG-2–/– mice lacking T cells, B cells, and NKT cells become highly prone to passive experimental autoimmune encephalomyelitis (EAE) after eliminating NK cells in vivo (18). " So these are not your daddys lab mice. Specifically, if they have no lymphocytes they must have no T-regulatory cells? Whats up with that? How are you going to expect them to have any immunological normality? From my very very crude knowledge of T-reg cells I dont think we know enough to exclude this being a big factor. Its kind of like studying injured animals to find out what kinds of stimuli provoke emotional irritation. " We have previously revealed that gut-shot chimps become highly prone to distress responses to loud noises after they have been treated with tear gas. " Further, there is the problem of " transfer dynamics " as I'll call it. Take this paper: " 5 × 10^6 T-line cells [ie 5 million cells of a single T-cell clone] were intravenously transferred. " We know that autoAbs and autoreactive T-cells occur at some level in various natural states of health and disease, and that there are mechanisms that keep autoreactivity to harmless levels at least in healthy individuals. How do we know that the sudden introduction of auto-T- cells, or autoAb for that matter, does not overcome self-tolerance regulatory networks in ways having nothing to do with any natural disease? This seems to be a potential problem with any adoptive/passive transfer experiment. Quote Link to comment Share on other sites More sharing options...
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