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Sunday, January 02, 2022 4:13:53 PM
As we all look forward toward better things, I have a question for those who understand this stuff better than me ... and it concerns a question that I asked Phantom, that he forwarded to Marker.
OK, the subject is Tumor Associated Antigens.
WE (MRKR) use 5 in our cocktail mix.
PRAME, SSX2, MAGEA4, SURVIVIN, and NY-ESO-1.
Now I assume those 5 were chosen after some reseach and determination that those 5 would be the most effective against AML.
I read this on tumor markers: https://www.cancer.gov/about-cancer/diagnosis-staging/diagnosis/tumor-markers-list
BOY, there sure is a lot of them for a whole bunch of different cancers, with different markers for different cancers.
And I read this: "The National Cancer Institute has recently published a priority list of 75 cancer antigens, providing a useful basis for those aiming to test vaccine design and operation against well-documented targets."
And then I read this ... of which ... OUR OWN DR. ALLISON was a part of: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5779623/
So my question is this.
Is using the same 5 antigens (PRAME, SSX2, MAGEA4, SURVIVIN, and NY-ESO-1) on cancers that are not AML still be substantially effective?
We know/assume they are great antigens for AML, but does ANYBODY KNOW they are good antigen targets for ... let's say, Pancreatic, or different blood/bone/brain/etc. cancers?
Or, would a different, more targeted antigen cocktail mix be better?
Anybody have an idea about what BOTH, the added time and the added money would be to research which 5 antigens (out of the 75) would be most effective against Pancreatic (the same kind of research they did to chose the 5 for AML)?
I don't want to intentionally oversimplify the complex FDA preclinical process but, you put some Pancreatic cancer cells in a glass dish, you introduce 1 of the 75 antigens, you see what happens, and then you do that with the other 74.
How long and expensive could that be?
Thank You All, let's have a better 2022.
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