Retrovirology

official impact factor 5.24

This article is part of the supplement: AIDS Vaccine 2009

Open Access Oral presentation

S021-06 OA. Potent and broad neutralizing antibodies from HIV-1 non-clade B infected donor reveal a new HIV-1 vaccine target

SK Phogat1*, L Walker2, D Wagner1, P Chan-Hui3, M Simek1, P Phung4, T Wrin4, J Mitcham3, P Investigator1, S Kaminsky1, T Zamb1, M Moyle3, W Koff1 and D Burton2

  • * Corresponding author: SK Phogat

Author Affiliations

1 AIDS Vaccine Design and Development Lab, IAVI, Brooklyn, NY, USA

2 Scripps Research Insitute, La Jolla, CA, USA

3 Theraclone Sciences, Seattle, WA, USA

4 Monogram Biosciences, San Franscisco, CA, USA

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Retrovirology 2009, 6(Suppl 3):O6 doi:10.1186/1742-4690-6-S3-O6

Published: 22 October 2009

First paragraph (this article has no abstract)

The ability to elicit broadly cross-reactive neutralizing antibodies is a major challenge in the development of an HIV-1 vaccine capable of neutralizing broad array of viruses in circulation. Nevertheless, a number of HIV-1 infected donors have broadly neutralizing sera and a handful of broadly neutralizing monoclonal antibodies have been isolated from clade B infected donors arguing that a vaccine strategy based upon eliciting broadly protective antibodies is feasible. These antibodies tend to display less breadth and potency against non-clade B viruses and they recognize epitopes on the virus that have so far proven refractory to incorporation into immunogens for elicitation of virus neutralizing responses.