Research project

C-Further: PRAME TCR-iNKT Therapy

Project overview

Despite significant advances in cancer treatment, many advanced childhood cancers—such as relapsed acute myeloid leukemia (AML), high-risk neuroblastoma, medulloblastoma (MB), and metastatic bone sarcomas, remain associated with poor survival rates. For example, relapsed AML survival rates are 20-40%, high-risk neuroblastoma is 50%, and relapsed neuroblastoma is less than 10%. Many of these cancers overexpress PRAME, a cancer-testis antigen, which presents a unique opportunity for targeted therapy. Autologous TCR-T cell therapies targeting PRAME have shown efficacy in adult melanoma, but for paediatric patients, allogeneic iNKT cells offer several advantages.

Staff

Lead researchers

Dr Ali Roghanian PhD, FHEA

Associate Professor
Research interests
  • Cancer immunotherapy
  • Monoclonal antibodies
  • Cellular therapies (e.g., CAR T and iNKT cells)
Connect with Ali

Other researchers

Dr Salah Mansour PhD

Associate Professor
Research interests
  • Unconventional T cells and lipid antigen recognition in human disease
  • CD1-restricted T cell immunity, including group 1 CD1, iNKT and γδ T cells
  • Molecular and structural mechanisms of CD1-mediated antigen presentation
Connect with Salah

Research outputs