| Literature DB >> 8023553 |
A J Conley1, P Conard, S Bondy, C A Dolan, J Hannah, W J Leanza, S Marburg, M Rivetna, V K Rusiecki, E E Sugg.
Abstract
A successful prophylactic human immunodeficiency virus type 1 (HIV-1) vaccine must elicit an immune response that will prevent establishment of the persistent viral infection. The only response shown to be effective in this regard is virus-neutralizing antibody directed against the viral gp120 hypervariable V3-loop region. Conjugate immunogens, containing cyclic peptides representing the V3 determinant covalently bound to a carrier protein, were capable of eliciting virus-neutralizing antibodies. The consistency of the response was related to peptide size. The smaller cyclic peptides, expressing relatively conserved sequences from the V3-loop apex, were poor inducers of neutralizing activity. In contrast, the largest cyclic peptides mediated neutralizing responses that were similar to those observed and previously reported for intact gp120 immunogens. A cyclic synthetic peptide expressing most of the prototypic HIV-1 MN variant V3 determinant warrants further study as a potentially effective vaccine immunogen.Entities:
Mesh:
Substances:
Year: 1994 PMID: 8023553 DOI: 10.1016/0264-410x(94)90123-6
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641