Guest guest Posted July 5, 2011 Report Share Posted July 5, 2011 I saw a new treatment has been patented for CFIDS/ME http://www.faqs.org/patents/app/20100331261 If you just google alpha 1 antitrypsin and CFS you get some info on it. The inventors are Quintana, Alegra . It's on the NCF webpage as well. I don't understand much about it. I understand that something called RNase L in the bodies of people w/CFS is abnormal. This alpha 1 trypsin is supposed to make it normal...I think (?) What I do understand is that this alpha-1 trypsin is prepared from human plasma. The FDA has approved of 3 alpha-1 trypsin products. They are given by infusion and treatment costs $100,000 a year. I was wondering if it were possible to get some cheaper substance that could do the same job. I read that alpha-1 trypsin is an elastase inhibitor and that raised elastase activity is what is causing the abnormal RNase L in the body of PWCFS. So I did my own google search for " natural elastase inhibitors " and got a lot of results with " indole-3-carbinol " in them. Here's just one: http://www.pnas.org/content/105/50/19750.full Indole 3 carbinol is available as a food supplement and supposed to be found naturally in brocolli and cabbage. Now I have too many severe digestive problems to buy and try this this supplement. If things were better I would have a go. This is just a suggestion but I wonder if it worthwhile for a PWCFS who can tolerate food supplements to try this and let us know how / if it helps. It does not look harmful - but I am just thinking aloud, I don't want to be resposible if someone takes it and finds they can't tolerate it. I was just wondering about it. What do others here think of this Spanish research? Quote Link to comment Share on other sites More sharing options...
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