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Synergy between dendritic cell-based vaccine and anti-CD137 monoclonal antibody in the treatment of mouse renal cell carcinoma
KMJ-Kuwait Medical Journal. 2012; 44 (4): 308-315
em En | IMEMR | ID: emr-171928
Biblioteca responsável: EMRO
Therapeutic efficacy of dendritic cell-based vaccine for renal cell carcinoma remains limited. In this study, we investigated whether anti-CD137 monoclonal antibody is capable of potentiating anti-tumor effect of dendritic cellbased vaccine. Experimental study. Research laboratory. Balb/c mice [8-10 weeks old]. A renal cell carcinoma model was established by subcutaneous injection of Renca tumor cells into Balb/c mice on day 0. After three days, tumor-bearing mice were treated with Renca tumor lysate-pulsed dendritic cells [i.e., dendritic cell-based vaccine], anti-CD137 monoclonal antibody, or combination of Renca tumor lysate-pulsed dendritic cells with anti-CD137 monoclonal antibody. Mice were killed on day 20 after tumor cell inoculation, and spleens were harvested for analysis of anti-tumor immune responses. The anti-tumor immune responses were analyzed by measuring proliferation and activity of T cells, which have the ability to kill tumor cells. The anti-tumor effect was assessed by measuring tumor size. The combination therapy with Renca tumor lysatepulsed dendritic cells and anti-CD137 antibody significantly increased T-cell proliferation and activity, and significantly inhibited tumor growth, compared with a single treatment with Renca tumor lysate-pulsed dendritic cells or anti-CD137 antibody. These results suggest that combination therapy can enhance anti-tumor effect by increasing T-cell proliferation and activity
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Índice: IMEMR Assunto principal: Células Dendríticas / Vacinas / Membro 9 da Superfamília de Receptores de Fatores de Necrose Tumoral / Imunoterapia / Neoplasias Renais / Camundongos Endogâmicos BALB C / Anticorpos Monoclonais Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Kuwait Med. J. Ano de publicação: 2012
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Índice: IMEMR Assunto principal: Células Dendríticas / Vacinas / Membro 9 da Superfamília de Receptores de Fatores de Necrose Tumoral / Imunoterapia / Neoplasias Renais / Camundongos Endogâmicos BALB C / Anticorpos Monoclonais Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Kuwait Med. J. Ano de publicação: 2012