A tetravalent recombinant dengue domain III protein vaccine stimulates neutralizing and enhancing antibodies in mice

被引:61
作者
Block, Olivia K. T. [2 ]
Rodrigo, W. W. Shanaka I. [2 ]
Quinn, Matthew [2 ]
Jin, Xia [2 ]
Rose, Robert C. [2 ]
Schlesinger, Jacob J. [1 ]
机构
[1] Univ Rochester, Med Ctr, Dept Med, Sch Med & Dent, Rochester, NY 14642 USA
[2] Univ Rochester, Dept Microbiol & Immunol, Sch Med & Dent, Rochester, NY 14642 USA
关键词
Dengue; Domain III; Vaccine; Enhancement; HUMAN-PAPILLOMAVIRUS TYPE-11; HIGH-LEVEL EXPRESSION; VIRUS-LIKE PARTICLES; ENVELOPE PROTEIN; ESCHERICHIA-COLI; DEPENDENT ENHANCEMENT; FLAVIVIRUS INFECTION; SUBUNIT VACCINE; P64K PROTEIN; IN-VITRO;
D O I
10.1016/j.vaccine.2010.10.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 Fc gamma R-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. (c) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:8085 / 8094
页数:10
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