Abstract:
:The functional help provided by four cross-linked synthetic peptides from HIV-1 Gag structural proteins was investigated in the mouse model. These peptides, selected upon non-self-criteria, are not predicted as T epitopes by classical prediction methods such as the Rothbard consensus or the amphipathy rule. Priming mice with these peptides allows the enhancement of the antibody response to HIV-1 Gag proteins (p55, p18, p24) given in the viral particle form. Furthermore, all of them also induce spleen and lymph node cells from primed mice to proliferate in vitro, in a MHC class II restricted context. This approach may help to identify relevant immunogenic viral epitopes that may be involved in a vaccinal strategy.
journal_name
Peptidesjournal_title
Peptidesauthors
Benveniste O,Vaslin B,Dormont Ddoi
10.1016/0196-9781(94)90055-8subject
Has Abstractpub_date
1994-01-01 00:00:00pages
935-43issue
6eissn
0196-9781issn
1873-5169pii
0196-9781(94)90055-8journal_volume
15pub_type
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