Clinical applications of virosomes in cancer immunotherapy

被引:15
作者
Adamina, Michel
Gullet, Ulrich
Bracci, Laura
Heberer, Michael
Spagnoli, Giulio C.
Schumacher, Reto
机构
[1] Univ Basel, Inst Surg Res & Hosp Management, CH-4031 Basel, Switzerland
[2] Univ Toronto, Dept Surg, Toronto, ON M5G 1X5, Canada
关键词
cancer immunotherapy; clinical trial; liposomes; virosomes;
D O I
10.1517/14712598.6.11.1113
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
Cancer immunotherapy is increasingly accepted as a treatment option for advanced stage disease. The identification of tumour-associated antigens in 1991 has prompted the development of antigen-specific immunotherapeutic strategies for a variety of cancers. Many of them result in some immunological responses in cancer patients; however, clinical results were not observed concomitantly with immunological responses; therefore, further improvements in the field of immunotherapy are urgently needed. Virosomes are lipidic envelopes devoid of genetic information, but which retain the antigenic profile and fusogenic properties from their viral origin. Virosomes are versatile antigen carriers and can be engineered to perform various tasks in cancer immunotherapy. Preclinical data have fostered the development of innovative clinical protocols. Hence, immunopotentiating reconstituted influenza virosomes will be assessed in breast and melanoma immunotherapy, and may contribute to the development of clinically effective cancer vaccines and ultimately improve patient outcomes. The objective of this review is to provide an overview of the potential clinical applications of virosomes as innovative and potentially effective reagents in active specific cancer immunotherapy.
引用
收藏
页码:1113 / 1121
页数:9
相关论文
共 69 条
[1]
Clinical applications of recombinant virus-based cancer immunotherapy [J].
Adamina, M ;
Daetwiler, S ;
Rosenthal, R ;
Zajac, P .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2005, 5 (09) :1211-1224
[2]
Encapsulation into sterically stabilised liposomes enhances the immunogenicity of melanoma-associated Melan-A/MART-1 epitopes [J].
Adamina, M ;
Bolli, M ;
Albo, F ;
Cavazza, A ;
Zajac, P ;
Padovan, E ;
Schumacher, R ;
Reschner, A ;
Feder, C ;
Marti, WR ;
Oertli, D ;
Heberer, M ;
Spagnoli, GC .
BRITISH JOURNAL OF CANCER, 2004, 90 (01) :263-269
[3]
Adamina M, 2005, SWISS MED WKLY, V135, P212
[4]
Advanced liposomal vectors as cancer vaccines in melanoma immunotherapy [J].
Adamina, Michel ;
Schumacher, Reto ;
Zajac, Paul ;
Weber, Walter P. ;
Rosenthal, Rachel ;
Groeper, Celia ;
Feder, Chantal ;
Zurbriggen, Rinaldo ;
Amacker, Mario ;
Spagnoli, Giulio C. ;
Oertli, Daniel ;
Heberer, Michael .
JOURNAL OF LIPOSOME RESEARCH, 2006, 16 (03) :195-204
[5]
Rapid induction of primary human CD4+ and CD8+ T cell responses against cancer-associated MUC1 peptide epitopes [J].
Agrawal, B ;
Krantz, MJ ;
Reddish, MA ;
Longenecker, BM .
INTERNATIONAL IMMUNOLOGY, 1998, 10 (12) :1907-1916
[6]
Degradation of the tumor antigen epitope gp100280-288 by fibroblast-associated enzymes abolishes specific immunorecognition [J].
Albo, F ;
Cavazza, A ;
Giardina, B ;
Marini, M ;
Roda, LG ;
Schumacher, R ;
Spagnoli, GC .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2004, 1671 (1-3) :59-69
[7]
ALMEIDA JD, 1975, LANCET, V2, P899
[8]
Peptide-loaded chimeric influenza virosomes for efficient in vivo induction of cytotoxic T cells [J].
Amacker, M ;
Engler, O ;
Kammer, AR ;
Vadrucci, S ;
Oberholzer, D ;
Cerny, A ;
Zurbriggen, R .
INTERNATIONAL IMMUNOLOGY, 2005, 17 (06) :695-704
[9]
Amoscato AA, 1998, J IMMUNOL, V161, P4023
[10]
Induction of cytotoxic T lymphocyte activity by fusion-active peptide-containing virosomes [J].
Arkema, A ;
Huckriede, A ;
Schoen, P ;
Wilschut, J ;
Daemen, T .
VACCINE, 2000, 18 (14) :1327-1333