Viral entry inhibitors block dengue antibody-dependent enhancement in vitro

被引:37
|
作者
Nicholson, Cindo O. [1 ]
Costin, Joshua M. [1 ]
Rowe, Dawne K. [1 ]
Lin, Li [2 ]
Jenwitheesuk, Ekachai [3 ]
Samudrala, Ram [4 ]
Isern, Sharon [1 ]
Michael, Scott F. [1 ]
机构
[1] Florida Gulf Coast Univ, Dept Biol Sci, Ft Myers, FL 33965 USA
[2] Tan Tock Seng Hosp, Communicable Dis Ctr, Singapore 308433, Singapore
[3] Natl Sci & Technol Dev Agcy, Natl Ctr Genet Engn & Biotechnol, Klongluang 12120, Pathumthani, Thailand
[4] Univ Washington, Dept Microbiol, Seattle, WA 98195 USA
关键词
Dengue; Antibody; Enhancement; Peptide; Entry; Inhibitor; HEMORRHAGIC-FEVER; VIRUS-INFECTION;
D O I
10.1016/j.antiviral.2010.11.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Severe dengue virus (DENV) disease symptoms, including dengue hemorrhagic fever and dengue shock syndrome, have been correlated with the presence of pre-existing antibodies that enhance rather than neutralize infections in Fc receptor bearing cells. These antibodies can originate from previous infection with a different serotype of dengue, or from waning antibody titers that occur in infants and young children as they are weaned from breast milk that contains protective dengue-specific antibodies. Despite the apparent importance of this antibody dependent enhancement (ADE) effect, there has been no description of any specific inhibitors of this process. We explored DENV entry inhibitors as a potential strategy to block ADE. Two different peptide entry inhibitors were tested for the ability to block antibody-mediated DENV-2 infection of human. FcRII bearing K562 cells in vitro. Both peptides were able to inhibit ADE, showing that entry inhibitors are possible candidates for the development of specific treatment for severe DENV infection. (C) 2010 Elsevier BM. All rights reserved.
引用
收藏
页码:71 / 74
页数:4
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