Abstract
The ultimate success of cancer vaccination is dependent upon the generation of tumor-specific CTLs. In this study, we designed and evaluated a novel fusion protein comprising a cell penetrating and immunostimulatory peptide corresponding to residues 32-51 of the Limulus polyphemus protein (LALF(32-51)) linked to human papillomavirus (HPV) 16 E7 antigen (LALF(32-51)-E7). We demonstrated that LALF(32-51) penetrates the cell membrane and delivers E7 into cells. In a preclinical model of HPV16-induced cervical carcinoma we showed that vaccination with adjuvant-free LALF(32-51)-E7 fusion protein significantly improves the presentation of E7-derived peptides to T-cells in vitro and induces suppression of tumor growth.
Copyright © 2010 Elsevier Ltd. All rights reserved.
MeSH terms
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Animals
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Carcinoma / immunology
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Carcinoma / prevention & control*
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Disease Models, Animal
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Female
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Horseshoe Crabs / genetics
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Horseshoe Crabs / immunology*
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Human papillomavirus 16 / genetics
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Human papillomavirus 16 / immunology*
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Mice
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Mice, Inbred C57BL
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Papillomavirus E7 Proteins / administration & dosage
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Papillomavirus E7 Proteins / genetics
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Papillomavirus E7 Proteins / immunology*
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Papillomavirus Infections / immunology
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Papillomavirus Infections / prevention & control*
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Papillomavirus Vaccines / administration & dosage
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Papillomavirus Vaccines / genetics
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Papillomavirus Vaccines / immunology*
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Recombinant Fusion Proteins / administration & dosage
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Recombinant Fusion Proteins / immunology
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Uterine Cervical Neoplasms / immunology
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Uterine Cervical Neoplasms / prevention & control*
Substances
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Papillomavirus E7 Proteins
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Papillomavirus Vaccines
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Recombinant Fusion Proteins
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oncogene protein E7, Human papillomavirus type 16