Dec 4, 2024
8:00pm - 8:00pm
Hynes, Level 1, Hall A
Shengnan Huang1,Yanpu He1,Allison Madow1,Huaiyao Peng1,Mirielle Griffin1,Jifa Qi1,Mantao Huang1,Nimrod Heldman1,Angela Belcher1
Massachusetts Institute of Technology1
Shengnan Huang1,Yanpu He1,Allison Madow1,Huaiyao Peng1,Mirielle Griffin1,Jifa Qi1,Mantao Huang1,Nimrod Heldman1,Angela Belcher1
Massachusetts Institute of Technology1
Vaccines stand as one of the most transformative innovations in medical science, safeguarding humanity by priming the immune system to combat pathogens. Building on this foundation, vaccines that closely mimic pathogen characteristics have proven highly effective in disease prevention. The M13 bacteriophage, with its inherent pathogen-like properties, offers a compelling and versatile platform for next-generation vaccine development. Its unique advantages include exceptional amenability to genetic engineering, a high safety profile, and robust stability under diverse conditions. In this study, we harness the M13 phage as a multifaceted candidate for peptide vaccines, which traditionally consist of an antigen, adjuvant, and delivery vehicle. By engineering the display of antigens on the M13 capsid protein and optimizing its adjuvant efficacy, we achieved a striking 20-fold enhancement in the antigen-specific CD8<sup>+</sup> T cell response. Furthermore, when integrated with immune checkpoint inhibitors, our M13 phage-based personalized vaccine led to the complete eradication of established tumors in preclinical models. These findings underscore the profound potential of the M13 phage as a groundbreaking platform for both vaccine design and cancer immunotherapy, opening new avenues for the development of highly effective, personalized treatments.