Dengue virus (DV) enhancing antibody activity in preillness plasma does not predict subsequent disease severity or viremia in secondary DV infection

被引:76
作者
Laoprasopwattana, K
Libraty, DH
Endy, TP
Nisalak, A
Chunsuttiwat, S
Vaughn, DW
Reed, G
Ennis, FA
Rothman, AL
Green, S
机构
[1] Univ Massachusetts, Sch Med, Ctr Infect Dis & Vaccine Res, Worcester, MA 01655 USA
[2] Univ Massachusetts, Sch Med, Dept Med, Div Prevent & Behav Med, Worcester, MA 01655 USA
[3] Walter Reed Army Inst Res, Dept Virus Res, Washington, DC USA
[4] USA, Med Res & Mat Command, Ft Detrick, MD USA
[5] Minist Publ Hlth, Div Gen Commun Dis, Dept Commun Dis Control, Bangkok, Thailand
[6] USA, Med Component, Dept Virol, Armed Forces Inst Med Sci, Bangkok, Thailand
[7] Songklanagarind Hosp, Dept Pediat, Songkhla, Thailand
关键词
D O I
10.1086/431520
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Dengue hemorrhagic fever, the most severe form of dengue illness, is associated with secondary dengue virus (DV) infection. Preexisting nonneutralizing antibodies to DV that enhance the infection of Fcg receptor bearing cells have been implicated in DV pathogenesis. Methods. We conducted a prospective cohort study in Thai schoolchildren. Enhancing activity (EA) was measured as the percentage of DV-infected K562 cells, and viral titer (infected K562 cell supernatants) was measured in preillness plasma samples from children who subsequently had secondary DV2 or DV3 infection. Results. Plaque-reduction neutralizing titers to the child's own DV2 or DV3 isolate were detected in 23 of 32 and 8 of 27 of the preillness plasma samples, and EA was detected to a low-passage Thai DV2 or DV3 in 31 of 32 and 26 of 27, respectively, of the samples. EA in undiluted preillness plasma did not correlate with subsequent disease severity or peak viremia levels in either secondary DV2 or DV3 infections. Conclusions. Preillness plasma enhances DV infection of K562 cells even in the presence of detectable neutralizing antibodies in LLC-MK2 cells. However, levels of preillness plasma EA of DV infection in K562 cells did not correlate with the clinical severity or viral burden of secondary DV infection.
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页码:510 / 519
页数:10
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