An immunocytometric assay based on dengue infection via DC-SIGN permits rapid measurement of anti-dengue neutralizing antibodies

被引:31
作者
Martin, Nicole C.
Pardo, Jorge
Simmons, Monika
Tjaden, Jeffrey A.
Widjaja, Susana
Marovich, Mary A.
Sun, Wellington
Porter, Kevin R.
Burgess, Timothy H.
机构
[1] USN, Med Res Ctr, Silver Spring, MD 20910 USA
[2] Walter Reed Army Inst Res, Silver Spring, MD 20910 USA
[3] Naval Med Res Unit 2, Jakarta 96520, Indonesia
[4] Uniformed Serv Univ Hlth Sci, Bethesda, MD 20814 USA
关键词
dengue virus; DC-SIGN; neutralization; PRNT; immunocytofluorimetry; dengue antibodies;
D O I
10.1016/j.jviromet.2005.12.002
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Dengue remains a global public health threat and development of a safe and effective vaccine is a principal public health goal. The primary correlate of immunity is thought to be neutralizing antibodies. Currently, the plaque reduction neutralization test (PRNT) is the gold standard measure of dengue neutralizing antibody responses, but this test is limited by time-consuming performance. In addition, some feel that use of viral strains adapted to grow in Vero or BHK cells may not accurately reflect protective responses. A human cell line transfected to express a putative natural dengue receptor, DC-SIGN (CD209), was used to measure antibody-mediated dengue neutralization. Using neutralizing monoclonal antibodies, immune sera, and laboratory adapted dengue viruses, serotype-specific neutralizing activity was demonstrated similar to that seen in the Vero PRNT. Importantly, serotype-specific neutralizing activity against recently isolated dengue strains with less heterotypic cross-neutralization than laboratory adapted viruses was also demonstrated. Published by Elsevier B.V.
引用
收藏
页码:74 / 85
页数:12
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