Affiliations 

  • 1 Research Centre for Biomedical Sciences, Sunway University, Kuala Lumpur, Malaysia
  • 2 Swinburne University of Technology, Melbourne, Australia
  • 3 James Cook University Clinical School, Cairns Base Hospital, Cairns, Queensland, Australia
  • 4 Queensland University of Technology, Brisbane, Queensland, Australia
  • 5 Australian Catholic University, Melbourne, Australia
PLoS One, 2016;11(5):e0155900.
PMID: 27223692 DOI: 10.1371/journal.pone.0155900

Abstract

Dengue virus (DENV) is a major public health threat worldwide. A key element in protection from dengue fever is the neutralising antibody response. Anti-dengue IgG purified from DENV-2 infected human sera showed reactivity against several peptides when evaluated by ELISA and epitope extraction techniques. A multi-step computational approach predicted six antigenic regions within the E protein of DENV-2 that concur with the 6 epitopes identified by the combined ELISA and epitope extraction approach. The selected peptides representing B-cell epitopes were attached to a known dengue T-helper epitope and evaluated for their vaccine potency. Immunization of mice revealed two novel synthetic vaccine constructs that elicited good humoral immune responses and produced cross-reactive neutralising antibodies against DENV-1, 2 and 3. The findings indicate new directions for epitope mapping and contribute towards the future development of multi-epitope based synthetic peptide vaccine.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.