Four cross-linked HIV Gag peptides prime the immune response to HIV proteins in mice.

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

Peptides

journal_title

Peptides

authors

Benveniste O,Vaslin B,Dormont D

doi

10.1016/0196-9781(94)90055-8

subject

Has Abstract

pub_date

1994-01-01 00:00:00

pages

935-43

issue

6

eissn

0196-9781

issn

1873-5169

pii

0196-9781(94)90055-8

journal_volume

15

pub_type

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