Abstract:
:For humoral immunization, it may be possible to make effective and safe peptide vaccines for various diseases by selection of proper B-cell epitopes. However, a lack of T-cell epitopes on short peptides, such as those associated with major histocompatibility complex (MHC)-restriction, is a major problem for peptide vaccine development. We propose a solution for the design of peptide vaccines that involves induction of broadly reactive T-cell epitopes via agretopes. The strategy involves positioning multi-agretope type peptides on the N-terminal side of a di-lysine linker and B-cell epitopes on the C-terminal side. The addition of the arginine-glysine-aspartate (RGD)-motif to the N terminus of the peptide enhances its immunogenicity, and enables nasal immunization without adjuvants.
journal_name
Vaccinejournal_title
Vaccineauthors
Yano A,Onozuka A,Asahi-Ozaki Y,Imai S,Hanada N,Miwa Y,Nisizawa Tdoi
10.1016/j.vaccine.2005.01.031subject
Has Abstractpub_date
2005-03-18 00:00:00pages
2322-6issue
17-18eissn
0264-410Xissn
1873-2518pii
S0264-410X(05)00034-4journal_volume
23pub_type
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