期刊
ACS CHEMICAL BIOLOGY
卷 13, 期 6, 页码 1668-1676出版社
AMER CHEMICAL SOC
DOI: 10.1021/acschembio.8b00313
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资金
- National Cancer Institute, National Institutes of Health [R01CA225101]
- Deutsche Forschungsgemeinschaft, DFG [WE 4751/2-1]
- Fonds der Chemischen Industrie [Li 184/01]
- Ministerium fur Kultur und Wissenschaft des Landes Nordrhein-Westfalen
- Bundesministerium fur Bildung und Forschung
- NATIONAL CANCER INSTITUTE [R01CA225105] Funding Source: NIH RePORTER
Mucin-1 (MUC1) is one of the top ranked tumor associated antigens. In order to generate effective anti-MUC1 immune responses as potential anticancer vaccines, MUC1 peptides and glycopeptides have been covalently conjugated to bacteriophage Q beta. Immunization of mice with these constructs led to highly potent antibody responses with IgG titers over one million, which are among the highest anti-MUC1 IgG titers reported to date. Furthermore, the high IgG antibody levels persisted for more than six months. The constructs also elicited MUC1 specific cytotoxic T cells, which can selectively kill MUC1 positive tumor cells. The unique abilities of Q beta-MUC1 conjugates to powerfully induce both antibody and cytotoxic T cell immunity targeting tumor cells bode well for future translation of the constructs as anticancer vaccines.
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