| Literature DB >> 20959154 |
Olivia K T Block1, W W Shanaka I Rodrigo, Matthew Quinn, Xia Jin, Robert C Rose, Jacob J Schlesinger.
Abstract
Dengue viruses co-circulate as four serologically distinct viruses (DENV1-4) that commonly infect individuals sequentially. Current DENV candidate vaccines incorporate the entire virion envelope E protein (E) ectodomain thereby stimulating both DENV serotype-specific and cross-reactive antibodies. Because the latter may enhance naturally acquired infection, such vaccine formulations must be tetravalent. We evaluated the neutralizing and enhancing antibody response to E domain III (dIII) proteins, in which serotype-specific neutralizing determinants are concentrated. Mice immunized with insect cell-secreted recombinant DENV-dIII proteins individually, and in tetravalent combination, produced serotype-specific IgG1 neutralizing antibodies that nevertheless exhibited measurable DENV enhancing activity in FcγR-bearing cells. Vaccine strategies directed to DENV-dIII-targeted neutralizing antibody production remain attractive but will likely require further modifications to induce safe, protective immunity.Entities:
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Year: 2010 PMID: 20959154 DOI: 10.1016/j.vaccine.2010.10.004
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641