Rankl and btn3a1 immunomodulatory ligands: MarsRecent Research Landscape
Standard immunotherapies fail when tumor cells evade T-cell recognition through low antigen presentation. These innovations engineer specific butyrophilin receptor activation and epigenetic modulation to restore immune visibility.
What technical problems is Mars addressing in Rankl and btn3a1 immunomodulatory ligands?
Insufficient immune system reconstitution
(20)evidences
Short biological half-life and rapid clearance of immunomodulatory agents limit treatment efficacy. Extending functional duration reduces dosing frequency and prevents premature therapeutic degradation.
Insufficient therapeutic tissue specificity
(12)evidences
Therapeutic agents often fail to accumulate at specific pathological sites like bone or cancer cells. Improving localization reduces off-target toxicity and enhances therapeutic efficacy.