Peter Attia· MD
and in fact now because we know the exact t- cell receptor sequences that we've cloned and isolated we it's almost an engineering problem because since we know the receptors we've now isolated libraries of receptors against p-53 K uh that we can now use to genetically modify lymphocytes to turn a normal lymphocyte that can attack the cancer and we have our first example of that now that we've submitted for publication targeting p53 by genetically altering a lymphocyte uh by giving it a receptor that could recognize some of these driver antigens