Joining the immunotherapy revolution: Adoptive cell therapy against cancer
|Professor Jose Villadangosfirstname.lastname@example.org||+61 3 903 57684||View page|
During cancer development, tumour cells generate neo-antigens on their surface, which can be recognized as foreign by cytotoxic CD8+ T lymphocytes (CTL). Following recognition of the tumour-associated antigens, tumour cells are targeted for elimination. A current cancer therapy in the clinic involves manufacture of tumour-specific CTL capable of destroying specifically tumour cells, and injection of the CTL into patients. While this revolutionary therapy shows great promise, impairment of the CTL in many patients prevents its full potential to be realised. To overcome these limitations, we are characterising the mechanisms that cause anti-cancer CTL inactivation.
Professor Jose Villadangos
Professor William Heath, Peter Doherty Institute
Dr Justine Mintern, Bioi21
Prato S, Mintern JD, Lahoud MH, Huang DC, Villadangos JA. Induction of antigen-specific effector-phase tolerance following vaccination against a previously ignored B-cell lymphoma. Immunol Cell Biol 2011; 89: 595-603.
Prato S, Zhan Y, Mintern JD, Villadangos JA. Rapid deletion and inactivation of CTLs upon recognition of a number of target cells over a critical threshold. J Immunol 2013; 191: 3534-3544.
Segal G, Prato S, Zehn D, Mintern JD, Villadangos JA. Target density, not affinity or avidity of antigen recognition, determines adoptive T cell therapy outcomes in a mouse lymphoma model. J Immunol 2016; In Press
Villadangos JA. Antigen-specific impairment of adoptive cell therapy against cancer: players, mechanisms, solutions and a hypothesis. Immunol Rev 2016; 272:169-182.
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