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Immunotherapy for prostate cancer: lessons from responses to tumor-associated antigens.
Westdorp, Harm; Sköld, Annette E; Snijer, Berit A; Franik, Sebastian; Mulder, Sasja F; Major, Pierre P; Foley, Ronan; Gerritsen, Winald R; de Vries, I Jolanda M.
Afiliación
  • Westdorp H; Department of Tumor Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center , Nijmegen , Netherlands ; Department of Medical Oncology, Radboud University Medical Center , Nijmegen , Netherlands.
  • Sköld AE; Department of Tumor Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center , Nijmegen , Netherlands.
  • Snijer BA; Department of Tumor Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center , Nijmegen , Netherlands.
  • Franik S; Department of Tumor Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center , Nijmegen , Netherlands.
  • Mulder SF; Department of Medical Oncology, Radboud University Medical Center , Nijmegen , Netherlands.
  • Major PP; Juravinski Hospital and Cancer Centre , Hamilton, ON , Canada.
  • Foley R; Juravinski Hospital and Cancer Centre , Hamilton, ON , Canada.
  • Gerritsen WR; Department of Medical Oncology, Radboud University Medical Center , Nijmegen , Netherlands.
  • de Vries IJ; Department of Tumor Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center , Nijmegen , Netherlands ; Department of Medical Oncology, Radboud University Medical Center , Nijmegen , Netherlands.
Front Immunol ; 5: 191, 2014.
Article en En | MEDLINE | ID: mdl-24834066
Prostate cancer (PCa) is the most common cancer in men and the second most common cause of cancer-related death in men. In recent years, novel therapeutic options for PCa have been developed and studied extensively in clinical trials. Sipuleucel-T is the first cell-based immunotherapeutic vaccine for treatment of cancer. This vaccine consists of autologous mononuclear cells stimulated and loaded with an immunostimulatory fusion protein containing the prostate tumor antigen prostate acid posphatase. The choice of antigen might be key for the efficiency of cell-based immunotherapy. Depending on the treatment strategy, target antigens should be immunogenic, abundantly expressed by tumor cells, and preferably functionally important for the tumor to prevent loss of antigen expression. Autoimmune responses have been reported against several antigens expressed in the prostate, indicating that PCa is a suitable target for immunotherapy. In this review, we will discuss PCa antigens that exhibit immunogenic features and/or have been targeted in immunotherapeutic settings with promising results, and we highlight the hurdles and opportunities for cancer immunotherapy.
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Front Immunol Año: 2014 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Front Immunol Año: 2014 Tipo del documento: Article País de afiliación: Países Bajos