Blame for treatment failures is usually attributed to so - called «cold» tumors, those that do not attract T - cell infiltration and may lack key T - cell targets — the mutated proteins known
as neoantigens.
Cancer cells may contain mutations in genes that code for antigens, producing misshapen or otherwise altered antigens that are known to scientists
as neoantigens.
Rather than simply identifying a cancer by location or tissue type, researchers now use advanced molecular profiling tests to characterize tumors, the proteins they express and the novel mutations they develop — known
as neoantigens.
Not exact matches
His work indicates that this cell surface marker could serve
as a target for a novel brain cancer vaccine or T - cell therapies engineered to recognize and kill tumors carrying that
neoantigen.
«Now that we can recognize cells altered by APOBEC3, we could teach tumor
neoantigen - based immunotherapies to recognize these cells
as well,» Pyeon says.
Algorithms, such
as NetMHC, have been developed in recent years, making it feasible to select HLA - binding
neoantigen peptides for the vaccine.
The researchers say the results warrant further development of
neoantigen vaccines, both alone and in combination with other immunotherapy weapons such
as checkpoint inhibitors.
Some cancers may have too many mutations to test
as potential
neoantigens.
However, identifying
neoantigens can still be useful
as cancer biomarkers.
In addition, it was increasingly recognized that oncolytic viruses not only were able to directly lyse cancer cells, but they also «freed «tumor specific
neoantigens, indirectly acting
as a cancer vaccine.
Our immuno - oncology product candidates are being developed in two separate approaches: one that targets specific antigens and / or epitopes (such
as CMB305 and in our
neoantigen collaboration); and an alternative approach that leverages the endogenous antigens found in the tumor microenvironment via intratumoral immunization (such
as G100).
Neoantigens — called so because they are newly formed during cancer development — may represent ideal immunotherapy targets
as they are solely expressed on tumor cells.
In addition to conserved antigens, these next - gen ZVex agents will be designed to produce personalized
neoantigen - based immunotherapies,
as well.
Instead of targeting specific tumor antigens, this approach relies on endogenous antigens (including
neoantigens) released during tumor lysis by treatments such
as chemotherapy or local radiation.
Designed to target multiple conserved antigens without antigen competition,
as well
as patient - specific
neoantigens, with immunostimulatory molecules