| Literature DB >> 25489968 |
Tzu-Yu Liu1, Waleed M Hussein, Ashwini Kumar Giddam, Zhongfan Jia, Jennifer M Reiman, Mehfuz Zaman, Nigel A J McMillan, Michael F Good, Michael J Monteiro, Istvan Toth, Mariusz Skwarczynski.
Abstract
Vaccination can provide a safe alternative to chemotherapy by using the body's natural defense mechanisms to create a potent immune response against tumor cells. Peptide-based therapeutic vaccines against human papillomavirus (HPV)-related cancers are usually designed to elicit cytotoxic T cell responses by targeting the HPV-16 E7 oncoprotein. However, peptides alone lack immunogenicity, and an additional adjuvant or external delivery system is required. In this study, we developed new polymer-peptide conjugates to create an efficient self-adjuvanting system for peptide-based therapeutic vaccines. These conjugates reduced tumor growth and eradicated E7-positive TC-1 tumors in mice after a "single shot" immunization, without the help from an external adjuvant. The new conjugates had a significantly higher anticancer efficacy than the antigen formulated with a commercial adjuvant. Furthermore, the polymer-peptide conjugates were promptly taken up by antigen presenting cells, including dendritic cells and macrophages, and efficiently activated CD4(+) T-helper cells and CD8(+) cytotoxic T lymphocyte cells.Entities:
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Year: 2014 PMID: 25489968 DOI: 10.1021/jm501514h
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446