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Plasma filter size/type used by Ron Davis?

Jesse2233

Senior Member
Messages
1,942
Location
Southern California
Does anyone know the plasma filter sized / type Ron used that still showed results on the impedance assay?

I'd like to provide this to my doctor for plasmapheresis

Thanks!
 
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JaimeS

Senior Member
Messages
3,408
Location
Silicon Valley, CA
Regarding what was done at the lab: this is an in vitro test, so it's far from being able to give us anything more than the most basic of cues regarding treatment. I understand that we are desperate for answers, and you have every right to make the best decisions you can about your health given the information available.

[Edited for clarity!]
 
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Jesse2233

Senior Member
Messages
1,942
Location
Southern California
Blood plasma isn't being filtered on that test. It's normal plasma that's been spun down in a centrifuge to separate it from RBCs etc. Perhaps I'm confused...

Got it, so particulates haven't started to be filtered out yet?

Know that no one at Stanford is recommending plasmapheresis as a therapy at this time, though.

Understood, I know things are very preliminary at this point
 

Jesse2233

Senior Member
Messages
1,942
Location
Southern California
Thanks @ljimbo423, any idea what that might correspond to on double filtration plasmapheresis (DFPP) in terms of micrometers?

upload_2017-5-23_13-54-51.png
 

Jesse2233

Senior Member
Messages
1,942
Location
Southern California
It would be between 10-2 and 10-3 micrometers.

Thanks Alice, very helpful. Having trouble interpreting some of these plasmapheresis technical documents, but they seem to be within that range

Oh, I see what you're referring to, after looking at that link!

When we perform the test on CFS plasma, the plasma is unfiltered. They're talking about filtering the plasma and the effect disappears. Gotcha!

Yes! :)

Does a filter size between 10-2 and 10-3 micrometers sound right to you?
 

Janet Dafoe

Board Member
Messages
867
Blood plasma isn't being filtered on that test. It's normal plasma that's been spun down in a centrifuge to separate it from RBCs etc. Perhaps I'm confused...

Regarding what was done at Stanford: this is an in vitro test, so it's far from being able to give us anything more than the most basic of cues regarding treatment. I understand that we are desperate for answers, and you have every right to make the best decisions you can about your health given the information available. Know that no one at Stanford is recommending plasmapheresis as a therapy at this time, though.

@Jesse2233, @JaimeS

Ron asked me to better clarify this. Ron says, "We have filtered the plasma to ascertain the size of the factor(s) that are causing the impedance change in our cell-based assay. The filter had a 10,000 molecular weight cut-off. When ME/CFS cells were exposed to the filtered plasma, they did not show a major increase in impedance, which made them look more like healthy controls.

"If a doctor asks us for information about what we are doing or what we have found, we can provide that information. However, we cannot make recommendations for or against any treatment or procedure to be done on a patient.

"I have no idea what other people at Stanford (outside the Genome Center) might recommend."
 

Alvin2

The good news is patients don't die the bad news..
Messages
3,023
I do wonder if donating blood is a bad idea for ME/CFS patients

@Jesse2233, @JaimeS

Ron asked me to better clarify this. Ron says, "We have filtered the plasma to ascertain the size of the factor(s) that are causing the impedance change in our cell-based assay. The filter had a 10,000 molecular weight cut-off. When ME/CFS cells were exposed to the filtered plasma, they did not show a major increase in impedance, which made them look more like healthy controls.
I know i'm asking for spoilers but can you tell us if they have identified the molecule(s) causing the block?
 

Sushi

Moderation Resource Albuquerque
Messages
19,935
Location
Albuquerque
I do wonder if donating blood is a bad idea for ME/CFS patients
Most would say yes for two reasons: Many of us don't have enough blood to begin with and two, we don't know whether we have stuff in our blood that would impact others. In some places it is illegal for ME/CFS patients to donate blood.
 

Alvin2

The good news is patients don't die the bad news..
Messages
3,023
Most would say yes for two reasons: Many of us don't have enough blood to begin with
Thats a good one, i LOLed :woot:
Probably the best reason :D
we don't know whether we have stuff in our blood that would impact others. In some places it is illegal for ME/CFS patients to donate blood
Of course, and i would agree with it not being allowed