Optimal organization of a polypeptide-based candidate cancer vaccine composed of cryptic tumor peptides with enhanced immunogenicity

被引:13
作者
Cornet, S
Miconnet, I
Menez, J
Lemonnier, F
Kosmatopoulos, K
机构
[1] Vaxon Biotech, F-91057 Evry, France
[2] Inst Pasteur, Unite Immunite Cellulaire Antivirale, F-75015 Paris, France
关键词
polypeptide; tumor vaccination; cryptic peptides;
D O I
10.1016/j.vaccine.2005.11.015
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Polyspecific tumor vaccination should offer broad control of tumor cells and reduce the risk of emergence of immune escape variants. Here, we evaluated the capacity of a polypeptide composed of optimized cryptic peptides derived from three different universal tumor antigens (TERT988Y, HER-2/neu(402Y) and MAGE-A(248V9)) to induce a polyspecific CD8 cell response both in vivo in HHD mice and in vitro in humans. A mixture of TERT988Y, HER-2/neu(402Y) and MAGE-A(248V9) peptides failed to induce a trispecific response. In contrast, a polypeptide composed of the three peptides stimulated a trispecific immune response. Interestingly, the capacity of the polypeptide to induce a trispecific response depended on its internal organization. Six different polypeptide variants corresponding to all possible combinations of the three peptides were tested. Only one variant, named Poly-6, elicited an immune response simultaneously targeting all three peptides. (c) 2006 Published by Elsevier Ltd.
引用
收藏
页码:2102 / 2109
页数:8
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