Synchronous apoptosis in established tumors leads to the induction of adaptive immunity.
dc.contributor.author | Honeychurch, Jamie | |
dc.contributor.author | Dive, Caroline | |
dc.contributor.author | Illidge, Timothy M | |
dc.date.accessioned | 2013-08-30T13:47:13Z | |
dc.date.available | 2013-08-30T13:47:13Z | |
dc.date.issued | 2013-06-01 | |
dc.identifier.citation | Synchronous apoptosis in established tumors leads to the induction of adaptive immunity. 2013, 2 (6):e24501 Oncoimmunology | en_GB |
dc.identifier.issn | 2162-4011 | |
dc.identifier.pmid | 23894711 | |
dc.identifier.doi | 10.4161/onci.24501 | |
dc.identifier.uri | http://hdl.handle.net/10541/300440 | |
dc.description.abstract | Understanding the immune response to the death of malignant cells is critical for the development of therapeutic strategies designed to stimulate the immune system against cancer. We have developed an inducible caspase-3-mediated death switch model to explore the effects of apoptosis on the host immune system, demonstrating that the synchronous apoptotic demise of established tumors can be immunogenic and elicit anticancer T-cell responses. | |
dc.language | ENG | |
dc.language.iso | en | en |
dc.rights | Archived with thanks to Oncoimmunology | en_GB |
dc.title | Synchronous apoptosis in established tumors leads to the induction of adaptive immunity. | en |
dc.type | Article | en |
dc.contributor.department | Targeted Therapy Group; Institute of Cancer Science; Paterson Institute for Cancer Research; Manchester University; Manchester Cancer Research Centre; Manchester Academic Health Sciences Centres; Manchester UK. | en_GB |
dc.identifier.journal | Oncoimmunology | en_GB |
html.description.abstract | Understanding the immune response to the death of malignant cells is critical for the development of therapeutic strategies designed to stimulate the immune system against cancer. We have developed an inducible caspase-3-mediated death switch model to explore the effects of apoptosis on the host immune system, demonstrating that the synchronous apoptotic demise of established tumors can be immunogenic and elicit anticancer T-cell responses. |