Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2014;10(10):3078-9.
doi: 10.4161/21645515.2014.972841.

Meeting report VLPNPV: Session 8: Vaccines I

Affiliations

Meeting report VLPNPV: Session 8: Vaccines I

David S Thiriot. Hum Vaccin Immunother. 2014.

Abstract

In Session 8 of the recent conference "Virus-Like Particle and Nano-Particle Vaccines" held at the Salk Institute in La Jolla, California (05 June 2014), four scientists described new virus-like particle (VLP) approaches, progress, and early-stage plans for vaccines against significant human pathogens including HPV, malaria, HIV, Dengue, and RSV. A unifying theme was that displaying epitopes in an array on a virus-like particle can be a powerful approach for achieving a strong immune response. VLP approaches described included display of epitopes on bacteriophage, display of epitopes as fusions with other protein multimerization domains, and self-assembly of recombinantly-expressed virus coat proteins. Another theme in some of the presentations was the targeting of neutralizing epitopes that are masked or only transiently accessible during natural infection.

Keywords: Bacteriophage display; E2 display; HIV (human immunodeficiency virus); HPV (human papillomavirus); RSV (respiratory syncytial virus); VLP (virus-like particle); dengue; malaria; vaccine development.

PubMed Disclaimer

Similar articles

Publication types

MeSH terms

LinkOut - more resources