Immunisation with 'naive' syngeneic dendritic cells protects mice from tumour challenge

Grimshaw MJ, Papazisis K, Picco G, Bohnenkamp H, Noll T, Taylor-Papadimitriou J, Burchell J (2008)
British Journal of Cancer 98(4): 784-791.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
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Grimshaw, M. J.; Papazisis, K.; Picco, G.; Bohnenkamp, H.; Noll, ThomasUniBi ; Taylor-Papadimitriou, J.; Burchell, J.
Abstract / Bemerkung
Dendritic cells (DCs) 'pulsed' with an appropriate antigen may elicit an antitumour immune response in mouse models. However, while attempting to develop a DC immunotherapy protocol for the treatment of breast cancer based on the tumour-associated MUC1 glycoforms, we found that unpulsed DCs can affect tumour growth. Protection from RMA-MUC1 tumour challenge was achieved in C57Bl/6 MUC1 transgenic mice by immunising with syngeneic DCs pulsed with a MUC1 peptide. However, unpulsed DCs gave a similar level of protection, making it impossible to evaluate the effect of immunisation of mice with DCs pulsed with the specific peptide. Balb/C mice could also be protected from tumour challenge by immunisation with unpulsed DCs prior to challenge with murine mammary tumour cells (410.4) or these cells transfected with MUC1 (E3). Protection was achieved with as few as three injections of 50 000 naive DCs per mouse per week, was not dependent on injection route, and was not specific to cell lines expressing human MUC1. However, the use of Rag2-knockout mice demonstrated that the adaptive immune response was required for tumour rejection. Injection of unpulsed DCs into mice bearing the E3 tumour slowed tumour growth. In vitro, production of IFN-gamma and IL-4 was increased in splenic cells isolated from mice immunised with DCs. Depleting CD4 T cells in vitro partially decreased cytokine production by splenocytes, but CD8 depletion had no effect. This paper shows that naive syngeneic DCs may induce an antitumour immune response and has implications for DC immunotherapy preclinical and clinical trials.
MUC1; immunotherapy; dendritic cell; breast cancer
British Journal of Cancer
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Grimshaw MJ, Papazisis K, Picco G, et al. Immunisation with 'naive' syngeneic dendritic cells protects mice from tumour challenge. British Journal of Cancer. 2008;98(4):784-791.
Grimshaw, M. J., Papazisis, K., Picco, G., Bohnenkamp, H., Noll, T., Taylor-Papadimitriou, J., & Burchell, J. (2008). Immunisation with 'naive' syngeneic dendritic cells protects mice from tumour challenge. British Journal of Cancer, 98(4), 784-791.
Grimshaw, M. J., Papazisis, K., Picco, G., Bohnenkamp, H., Noll, T., Taylor-Papadimitriou, J., and Burchell, J. (2008). Immunisation with 'naive' syngeneic dendritic cells protects mice from tumour challenge. British Journal of Cancer 98, 784-791.
Grimshaw, M.J., et al., 2008. Immunisation with 'naive' syngeneic dendritic cells protects mice from tumour challenge. British Journal of Cancer, 98(4), p 784-791.
M.J. Grimshaw, et al., “Immunisation with 'naive' syngeneic dendritic cells protects mice from tumour challenge”, British Journal of Cancer, vol. 98, 2008, pp. 784-791.
Grimshaw, M.J., Papazisis, K., Picco, G., Bohnenkamp, H., Noll, T., Taylor-Papadimitriou, J., Burchell, J.: Immunisation with 'naive' syngeneic dendritic cells protects mice from tumour challenge. British Journal of Cancer. 98, 784-791 (2008).
Grimshaw, M. J., Papazisis, K., Picco, G., Bohnenkamp, H., Noll, Thomas, Taylor-Papadimitriou, J., and Burchell, J. “Immunisation with 'naive' syngeneic dendritic cells protects mice from tumour challenge”. British Journal of Cancer 98.4 (2008): 784-791.

1 Zitation in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

MUC1 immunotherapy.
Beatson RE, Taylor-Papadimitriou J, Burchell JM., Immunotherapy 2(3), 2010
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