Neuroblastoma is one of the most common solid tumours to occur in children. It can be exceptionally difficult to treat and, despite intensive treatment, around one third of patients cannot currently be cured. In this project, Dr Gilham is harnessing the power of the immune system by engineering specific immune cells to destroy tumour cells. He will lay the essential groundwork in the laboratory to enable progression to clinical trial in children.
The genetics of familial leukaemia
Dr David Gilham
Paterson Institute for Cancer Research
29 March 2013
Neuroblastoma is the second most common solid tumour in childhood, affecting just under 100 children a year in ...Read more
Neuroblastoma is one of the most common solid tumours to occur in children, predominantly affecting children under the age of five years.
Around 40% of children diagnosed with neuroblastoma have a high-risk form that is essentially incurable using conventional treatments (chemotherapy, radiotherapy, surgery).
Immunotherapy approaches, turning the power of the immune system against the tumour, have already shown considerable promise in the treatment of neuroblastoma.
The immune system consists of a variety of different cells that protect us against pathogens like bacteria and viruses. Certain immune cells called T cells have the potential to kill tumour cells, but unfortunately tumours have an armoury of mechanisms that enable them to avoid recognition and eradication.
Gene therapy has been used to modify T cells, adding proteins called T cell receptors that can overcome some of these tumour defence systems. Early phase clinical studies of this T cell therapy have shown promise but, on their own, these T cell receptors lack the ability to fully activate the T cell.
In this project, Dr Gilham and colleagues will generate and test additional proteins, called “chimeric antigen receptors” (“CAR”), that can fully activate T cells thereby enhancing their anti-tumour potential.
The obvious benefit of this work is the potential to improve survival in children with neuroblastoma. If the technology functions optimally, it is strongly possible that the T cells may fight the local tumour and then provide a long-lived population of cells that could potentially fight recurring tumour cells at later times, thus guarding against relapse.
The research team incorporates scientists and clinicians with strong interests in the immune therapy of cancer and neuroblastoma. Dr Gilham has worked for more than 15 years in the field of T cell therapy for cancer and along with his colleague Professor Robert Hawkins has developed the research group and the infrastructure to deliver these new therapies. They are working with Dr Guy Makin, the national lead for phase II neuroblastoma clinical trials, ideally placing them to bring new therapies rapidly to the clinic for the benefit of children with poor prognosis neuroblastoma.
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