Guest guest Posted April 16, 2006 Report Share Posted April 16, 2006 > For all you DIYs > Regards > Windsor > > http://www.lyme-diagnosis.org.uk/ Lord, I wish that level of cash would do it. I'd be doing this in an instant. Unfortunately these bodies cant be ID'd, and could be derived from red cell membranes etc. I've run across claims that these do not appear, and contrary claims that they often DO appear, in healthy controls - but I havent seen a large data set either way. They cant be concluded to be microbial based on what we see here; if they are I dont know how we know they arent contaminants. It takes some hours for them to appear, I hear, which is plenty of time for a few contaminating microbes to multiply greatly. Fluorescent antibody against Bb would go a long way towards determining whether these are Bb; fluorescin-conjugated murimidase would probably be very helpful in determining whether they are bacterial at all. I wish I could get a fluorescence scope. Damn, do I wish. But they cost a pretty penny. Thats what the Bowen test is using. But I've not seen anything from Bowen about whether what theyre seeing is also found in healthy controls, or is reduced in improved patients, etc. Thats too bad. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 16, 2006 Report Share Posted April 16, 2006 Dear You are spot on , of course. The problem appears to be that no one has set up the whole gamut of testing on a reference population, and then gone back and analysed the test differences in the light of individual biochemical differences in the patient ( perhaps correlated with disease stage) I grew up in the area of Australia now known to be the focal point of tick borne infections. Had my first tick nearly 50 years ago, can trace my downhill progress from that point. Tested equivocal to Borellia in the early days when burgdorferi antigens were the only ones testable. Now clear but don't believe one bit of it Regards Windsor [infections] Re: How to see Borrelia Bergdoferi using a microscope > > > For all you DIYs > > Regards > > Windsor > > > > http://www.lyme-diagnosis.org.uk/ > > Lord, I wish that level of cash would do it. I'd be doing this in an > instant. Unfortunately these bodies cant be ID'd, and could be derived > from red cell membranes etc. I've run across claims that these do not > appear, and contrary claims that they often DO appear, in healthy > controls - but I havent seen a large data set either way. They cant be > concluded to be microbial based on what we see here; if they are I dont > know how we know they arent contaminants. It takes some hours for them > to appear, I hear, which is plenty of time for a few contaminating > microbes to multiply greatly. > > Fluorescent antibody against Bb would go a long way towards determining > whether these are Bb; fluorescin-conjugated murimidase would probably > be very helpful in determining whether they are bacterial at all. I > wish I could get a fluorescence scope. Damn, do I wish. But they cost a > pretty penny. Thats what the Bowen test is using. But I've not seen > anything from Bowen about whether what theyre seeing is also found in > healthy controls, or is reduced in improved patients, etc. Thats too > bad. > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 29, 2006 Report Share Posted April 29, 2006 Bela Bozsik is using a flourescent monoclonal antibodies to detect borrelia. He spoke at the Tick-bourne Diseases conference in Sheffield, UK, last June. AW says that his patients are testing positive with Bozsik's technique. That's not conclusive proof that what he's seeng is borrelia but is highly suggestive. I have no idea whether healthy controls have been tested. Sue > Lord, I wish that level of cash would do it. I'd be doing this in an > instant. Unfortunately these bodies cant be ID'd, and could be > derived from red cell membranes etc. I've run across claims that > these do not appear, and contrary claims that they often DO appear, > in healthy controls - but I havent seen a large data set either way. > They cant be concluded to be microbial based on what we see here; if > they are I dont know how we know they arent contaminants. It takes > some hours for them to appear, I hear, which is plenty of time for a > few contaminating microbes to multiply greatly. > > Fluorescent antibody against Bb would go a long way towards determining > whether these are Bb; fluorescin-conjugated murimidase would probably > be very helpful in determining whether they are bacterial at all. I > wish I could get a fluorescence scope. Damn, do I wish. But they cost a > pretty penny. Thats what the Bowen test is using. But I've not seen > anything from Bowen about whether what theyre seeing is also found in > healthy controls, or is reduced in improved patients, etc. Thats too > bad. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 29, 2006 Report Share Posted April 29, 2006 Thanks for the info ,I just google Bela Bozsik & came up with this ..some useful info on combination therapy.. http://www.lymediseaseaction.org.uk/conf2005/bozsik2/bozsik_sat.html [infections] Re: How to see Borrelia Bergdoferi using a microscope Bela Bozsik is using a flourescent monoclonal antibodies to detect borrelia. He spoke at the Tick-bourne Diseases conference in Sheffield, UK, last June. AW says that his patients are testing positive with Bozsik's technique. That's not conclusive proof that what he's seeng is borrelia but is highly suggestive. I have no idea whether healthy controls have been tested. Sue > Lord, I wish that level of cash would do it. I'd be doing this in an > instant. Unfortunately these bodies cant be ID'd, and could be > derived from red cell membranes etc. I've run across claims that > these do not appear, and contrary claims that they often DO appear, > in healthy controls - but I havent seen a large data set either way. > They cant be concluded to be microbial based on what we see here; if > they are I dont know how we know they arent contaminants. It takes > some hours for them to appear, I hear, which is plenty of time for a > few contaminating microbes to multiply greatly. > > Fluorescent antibody against Bb would go a long way towards determining > whether these are Bb; fluorescin-conjugated murimidase would probably > be very helpful in determining whether they are bacterial at all. I > wish I could get a fluorescence scope. Damn, do I wish. But they cost a > pretty penny. Thats what the Bowen test is using. But I've not seen > anything from Bowen about whether what theyre seeing is also found in > healthy controls, or is reduced in improved patients, etc. Thats too > bad. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 29, 2006 Report Share Posted April 29, 2006 I think thats roughly as close to proof as you can get. I guess robust cross-reaction of specific antibody can happen, but a great deal of molecular biology is based on the notion that its very rare. For example, antibody-specificity-based assays like western blots and ELISAs are used not only for diagnosis, but also for various sorts of scientific investigations all over medical and non-medical biology. I just wish we could get the research establishment interested in this. " tensevern " <tensevern@...> wrote: > > Bela Bozsik is using a flourescent monoclonal antibodies to detect > borrelia. He spoke at the Tick-bourne Diseases conference in > Sheffield, UK, last June. AW says that his patients are testing > positive with Bozsik's technique. That's not conclusive proof that > what he's seeng is borrelia but is highly suggestive. I have no idea > whether healthy controls have been tested. > > Sue > > > > Lord, I wish that level of cash would do it. I'd be doing this in an > > instant. Unfortunately these bodies cant be ID'd, and could be > > derived from red cell membranes etc. I've run across claims that > > these do not appear, and contrary claims that they often DO appear, > > in healthy controls - but I havent seen a large data set either way. > > They cant be concluded to be microbial based on what we see here; if > > they are I dont know how we know they arent contaminants. It takes > > some hours for them to appear, I hear, which is plenty of time for a > > few contaminating microbes to multiply greatly. > > > > Fluorescent antibody against Bb would go a long way towards determining > > whether these are Bb; fluorescin-conjugated murimidase would probably > > be very helpful in determining whether they are bacterial at all. I > > wish I could get a fluorescence scope. Damn, do I wish. But they cost a > > pretty penny. Thats what the Bowen test is using. But I've not seen > > anything from Bowen about whether what theyre seeing is also found in > > healthy controls, or is reduced in improved patients, etc. Thats too > > bad. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 1, 2006 Report Share Posted May 1, 2006 I just watched Dr Gows DVD. It seems his approach is very thorough. He started with a gene chip. Many groups studying gene expression stop there. But he also is using RT-PCR and western blots to confirm the numbers on genes whose expression is substantially different in CFS. Furthermore, to make sure the antibody isnt binding cross-reactively in the western blots, he has been recovering the proteins to send them in for mass spectroscopy, which can identify them definitevely. This is one example of a person not being satisfied to rest on the specificity of the antibody in a western blot; instead he takes a further measure. But I have seen many other cases where people publish western blot data without mass spec to confirm it. Im totally impressed with what Gow is doing, tho it remains preliminary so far. " " <usenethod@...> wrote: > > I think thats roughly as close to proof as you can get. I guess > robust cross-reaction of specific antibody can happen, but a great > deal of molecular biology is based on the notion that its very rare. > For example, antibody-specificity-based assays like western blots and > ELISAs are used not only for diagnosis, but also for various sorts of > scientific investigations all over medical and non-medical biology. > > I just wish we could get the research establishment interested in > this. > > > " tensevern " <tensevern@> wrote: > > > > Bela Bozsik is using a flourescent monoclonal antibodies to detect > > borrelia. He spoke at the Tick-bourne Diseases conference in > > Sheffield, UK, last June. AW says that his patients are testing > > positive with Bozsik's technique. That's not conclusive proof that > > what he's seeng is borrelia but is highly suggestive. I have no idea > > whether healthy controls have been tested. > > > > Sue Quote Link to comment Share on other sites More sharing options...
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