4.8 Article

Proof of principle for epitope-focused vaccine design

期刊

NATURE
卷 507, 期 7491, 页码 201-206

出版社

NATURE PORTFOLIO
DOI: 10.1038/nature12966

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资金

  1. Fundacao para a Ciencia e a Tecnologia [SFRH/BD/32958/2006]
  2. National Institutes of Health NRSA Training Grant [T32CA080416]
  3. Children's Hospital of Philadelphia
  4. Bill and Melinda Gates Foundation CAVD award
  5. International AIDS Vaccine Initiative Neutralizing Antibody Consortium
  6. International AIDS Vaccine Initiative Neutralizing Antibody Center
  7. March of Dimes
  8. National Institutes of Health [2T32GM007270, U54 AI 005714]
  9. National Institute of Allergy and Infectious Diseases [P01AI094419, 5R21AI088554, 1UM1AI100663, 1R01AI102766-01A1]
  10. National Institute of Allergy and Infectious Diseases from the Center for AIDS Research, University of California, San Diego [P30AI36214]
  11. Fundação para a Ciência e a Tecnologia [SFRH/BD/32958/2006] Funding Source: FCT

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Vaccines prevent infectious disease largely by inducing protective neutralizing antibodies against vulnerable epitopes. Several major pathogens have resisted traditional vaccine development, although vulnerable epitopes targeted by neutralizing antibodies have been identified for several such cases. Hence, new vaccine design methods to induce epitope-specific neutralizing antibodies are needed. Here we show, with a neutralization epitope from respiratory syncytial virus, that computational protein design can generate small, thermally and conformationally stable protein scaffolds that accurately mimic the viral epitope structure and induce potent neutralizing antibodies. These scaffolds represent promising leads for the research and development of a human respiratory syncytial virus vaccine needed to protect infants, young children and the elderly. More generally, the results provide proof of principle for epitope-focused and scaffold-based vaccine design, and encourage the evaluation and further development of these strategies for a variety of other vaccine targets, including antigenically highly variable pathogens such as human immunodeficiency virus and influenza.

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