Abstract |
The efficacy of phage display particles expressing tumor antigen P1A35-43 in inducing protective and therapeutic anti- tumor immune responses were studied. A protective immune response against a lethal progressive P815 mastocytoma tumor cell challenge was established after subcutaneous injection of phage display particles. Furthermore, the vaccine suppressed growth of pre-existing tumors. Immunization with the hybrid phage particles elicited P1A(35-43) specific CTL responses and a Th1-dominated immune response with phage particle-specific secretion of IFN-gamma but not IL-4. Our results indicate that phage display particles might be a useful vaccine form for tumor-associated antigen epitopes in tumor immunotherapy.
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Authors | Yuzhang Wu, Ying Wan, Jiang Bian, Jianping Zhao, ZhengCai Jia, Liyun Zhou, Wei Zhou, Yang Tan |
Journal | International journal of cancer
(Int J Cancer)
Vol. 98
Issue 5
Pg. 748-53
(Apr 10 2002)
ISSN: 0020-7136 [Print] United States |
PMID | 11920646
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright 2002 Wiley-Liss, Inc. |
Chemical References |
- DNA Primers
- Peptide Fragments
- Peptide Library
- Chromium
- Interleukin-4
- Interferon-gamma
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Topics |
- Animals
- Base Sequence
- Chromium
(metabolism)
- DNA Primers
- Immunotherapy
- Interferon-gamma
(metabolism)
- Interleukin-4
(metabolism)
- Male
- Mice
- Mice, Inbred DBA
- Molecular Sequence Data
- Neoplasms, Experimental
(immunology, mortality, therapy)
- Peptide Fragments
(immunology)
- Peptide Library
- Plasmids
- Survival Rate
- Th1 Cells
(immunology)
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