Potential Target Antigens for a Universal Vaccine in Epithelial Ovarian Cancer

The prognosis of epithelial ovarian cancer (EOC), the primary cause of death from gynaecological malignancies, has only modestly improved over the last decades. Immunotherapeutic treatment using a cocktail of antigens has been proposed as a “universal” vaccine strategy. We determined the expression...

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Main Authors: Renee Vermeij, Toos Daemen, Geertruida H. de Bock, Pauline de Graeff, Ninke Leffers, Annechien Lambeck, Klaske A. ten Hoor, Harry Hollema, Ate G. J. van der Zee, Hans W. Nijman
Format: Article
Language:English
Published: Wiley 2010-01-01
Series:Clinical and Developmental Immunology
Online Access:http://dx.doi.org/10.1155/2010/891505
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author Renee Vermeij
Toos Daemen
Geertruida H. de Bock
Pauline de Graeff
Ninke Leffers
Annechien Lambeck
Klaske A. ten Hoor
Harry Hollema
Ate G. J. van der Zee
Hans W. Nijman
author_facet Renee Vermeij
Toos Daemen
Geertruida H. de Bock
Pauline de Graeff
Ninke Leffers
Annechien Lambeck
Klaske A. ten Hoor
Harry Hollema
Ate G. J. van der Zee
Hans W. Nijman
author_sort Renee Vermeij
collection DOAJ
description The prognosis of epithelial ovarian cancer (EOC), the primary cause of death from gynaecological malignancies, has only modestly improved over the last decades. Immunotherapeutic treatment using a cocktail of antigens has been proposed as a “universal” vaccine strategy. We determined the expression of tumor antigens in the context of MHC class I expression in 270 primary tumor samples using tissue microarray. Expression of tumor antigens p53, SP17, survivin, WT1, and NY-ESO-1 was observed in 120 (48.0%), 173 (68.9%), 208 (90.0%), 129 (56.3%), and 27 (11.0%) of 270 tumor specimens, respectively. In 93.2% of EOC, at least one of the investigated tumor antigens was (over)expressed. Expression of MHC class I was observed in 78.1% of EOC. In 3 out 4 primary tumors, (over)expression of a tumor antigen combined with MHC class I was observed. These results indicate that a multiepitope vaccine, comprising these antigens, could serve as a universal therapeutic vaccine for the vast majority of ovarian cancer patients.
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spelling doaj-art-3a3d1eab845a458bb2b9a343d01850622025-02-03T00:59:47ZengWileyClinical and Developmental Immunology1740-25221740-25302010-01-01201010.1155/2010/891505891505Potential Target Antigens for a Universal Vaccine in Epithelial Ovarian CancerRenee Vermeij0Toos Daemen1Geertruida H. de Bock2Pauline de Graeff3Ninke Leffers4Annechien Lambeck5Klaske A. ten Hoor6Harry Hollema7Ate G. J. van der Zee8Hans W. Nijman9Department of Gynecological Oncology, University Medical Center Groningen, University of Groningen, P.O. Box 30.001, 9700 RB Groningen, The NetherlandsDepartment of Medical Microbiology, Molecular Virology Section, University Medical Center Groningen, University of Groningen, P.O. Box 30.001, 9700 RB Groningen, The NetherlandsDepartment of Epidemiology, University Medical Center Groningen, University of Groningen, P.O. Box 30.001, 9700 RB Groningen, The NetherlandsDepartment of Gynecological Oncology, University Medical Center Groningen, University of Groningen, P.O. Box 30.001, 9700 RB Groningen, The NetherlandsDepartment of Gynecological Oncology, University Medical Center Groningen, University of Groningen, P.O. Box 30.001, 9700 RB Groningen, The NetherlandsDepartment of Gynecological Oncology, University Medical Center Groningen, University of Groningen, P.O. Box 30.001, 9700 RB Groningen, The NetherlandsDepartment of Gynecological Oncology, University Medical Center Groningen, University of Groningen, P.O. Box 30.001, 9700 RB Groningen, The NetherlandsDepartment of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, P.O. Box 30.001, 9700 RB Groningen, The NetherlandsDepartment of Gynecological Oncology, University Medical Center Groningen, University of Groningen, P.O. Box 30.001, 9700 RB Groningen, The NetherlandsDepartment of Gynecological Oncology, University Medical Center Groningen, University of Groningen, P.O. Box 30.001, 9700 RB Groningen, The NetherlandsThe prognosis of epithelial ovarian cancer (EOC), the primary cause of death from gynaecological malignancies, has only modestly improved over the last decades. Immunotherapeutic treatment using a cocktail of antigens has been proposed as a “universal” vaccine strategy. We determined the expression of tumor antigens in the context of MHC class I expression in 270 primary tumor samples using tissue microarray. Expression of tumor antigens p53, SP17, survivin, WT1, and NY-ESO-1 was observed in 120 (48.0%), 173 (68.9%), 208 (90.0%), 129 (56.3%), and 27 (11.0%) of 270 tumor specimens, respectively. In 93.2% of EOC, at least one of the investigated tumor antigens was (over)expressed. Expression of MHC class I was observed in 78.1% of EOC. In 3 out 4 primary tumors, (over)expression of a tumor antigen combined with MHC class I was observed. These results indicate that a multiepitope vaccine, comprising these antigens, could serve as a universal therapeutic vaccine for the vast majority of ovarian cancer patients.http://dx.doi.org/10.1155/2010/891505
spellingShingle Renee Vermeij
Toos Daemen
Geertruida H. de Bock
Pauline de Graeff
Ninke Leffers
Annechien Lambeck
Klaske A. ten Hoor
Harry Hollema
Ate G. J. van der Zee
Hans W. Nijman
Potential Target Antigens for a Universal Vaccine in Epithelial Ovarian Cancer
Clinical and Developmental Immunology
title Potential Target Antigens for a Universal Vaccine in Epithelial Ovarian Cancer
title_full Potential Target Antigens for a Universal Vaccine in Epithelial Ovarian Cancer
title_fullStr Potential Target Antigens for a Universal Vaccine in Epithelial Ovarian Cancer
title_full_unstemmed Potential Target Antigens for a Universal Vaccine in Epithelial Ovarian Cancer
title_short Potential Target Antigens for a Universal Vaccine in Epithelial Ovarian Cancer
title_sort potential target antigens for a universal vaccine in epithelial ovarian cancer
url http://dx.doi.org/10.1155/2010/891505
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