4.2 Article

Presenting native-like HIV-1 envelope trimers on ferritin nanoparticles improves their immunogenicity

Journal

RETROVIROLOGY
Volume 12, Issue -, Pages -

Publisher

BMC
DOI: 10.1186/s12977-015-0210-4

Keywords

HIV-1; Envelope glycoprotein; Ferritin; Nanoparticles; Vaccine; SOSIP; BG505

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Funding

  1. International AIDS Vaccine Initiative (IAVI)
  2. Bill and Melinda Gates Foundation
  3. National Institutes of Health Grant [P01 AI082362]
  4. NIAID-NIH Contract [HHSN27201100016C]
  5. Scripps CHAVI-ID [UM1 AI100663]
  6. Netherlands Organization for Scientific Research (NWO)
  7. European Research Council [ERC-StG-2011-280829-SHEV]

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Background: Presenting vaccine antigens in particulate form can improve their immunogenicity by enhancing B cell activation. Findings: We describe ferritin-based protein nanoparticles that display multiple copies of native-like HIV-1 envelope glycoprotein trimers (BG505 SOSIP.664). Trimer-bearing nanoparticles were significantly more immunogenic than trimers in both mice and rabbits. Furthermore, rabbits immunized with the trimer-bearing nanoparticles induced significantly higher neutralizing antibody responses against most tier 1A viruses, and higher responses ( but not significantly), to several tier 1B viruses and the autologous tier 2 virus than when the same trimers were delivered as soluble proteins. Conclusions: This or other nanoparticle designs may be practical ways to improve the immunogenicity of envelope glycoprotein trimers.

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