YSC Session
KLH-GP2-P4 peptide, derived from HER2 receptor of breast cancer tumor, serves as tumor-associated antigen in breast cancer vaccines (2). Cancer cell membrane (CCM) coating on vaccine formulation enhances immune recognition by mimicking native tumor antigens andĀ providing moreĀ potent tumor-specific antigens (1). In this study, liposomes (LP) loaded with KLH-GP2-P4 are coated with CCM derived from either TUBO or 4T1 cells. We evaluate how different CCM sources influence vaccine specificity and personalization, providing insights into tailored cancer immunotherapy with biomimetic nanoparticles.
Anushri Sambanthan, PhD Candidate (she/her/hers)
PhD Candidate
National University of Malaysia
BATANG KALI, Selangor, Malaysia