A report published in The Journal of Experimental Medicine suggests that scientists have found a way to find the proverbial needle in the cancer antigen haystack.

But here's the catch. These prediction tools generate hundreds of possible neoepitopes, of which only a handful can actually elicit T cells capable of attacking the tumor. And so far, there has been no reliable common denominator to help pinpoint this useful handful.
Previous attempts to predict cancer neoepitopes have relied on how strongly the mutated protein is recognized by the immune system. But scientists at the University of Connecticut now show that the strength of this interaction is a poor predictor. A better (albeit still imperfect) measure turns out to be how different the mutation looks to the T cell when compared to its normal counterpart—the more distinct, the better. These results have the potential to completely change current approaches to generating anticancer vaccines.
Source-Eurekalert
MEDINDIA




Email






