Comparison of capture immunoglobulin M (IgM) and IgG enzyme-linked immunosorbent assay (ELISA) and nonstructural protein NS1 serotype-specific IgG ELISA for differentiation of primary and secondary dengue virus infections

被引:150
作者
Shu, PY
Chen, LK
Chang, SF
Yueh, YY
Chow, L
Chien, LJ
Chin, C
Lin, TH
Huang, JH
机构
[1] Ctr Dis Control, Dept Hlth, Div Res Dev & Lab Diagnosis, Taipei, Taiwan
[2] Co Wealth Med Sci & Biotechnol, Taipei, Taiwan
[3] Tzu Chi Coll Med, Dept Emergency Med, Ctr Med, Hualien, Taiwan
关键词
D O I
10.1128/CDLI.10.4.622-630.2003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have found that NS1 serotype-specific immunoglobulin G (IgG) enzyme-linked immunosorbent assay (ELISA) can be used to differentiate primary and secondary dengue virus infections. This is due to the fact that the NS1-specific IgG antibody cannot be detected before day 9 of illness for primary infection, so the NS1-specific IgG antibodies measured in acute-phase sera must come from previous infection. Comparison of NS1 serotype-specific IgG ELISA with envelope- and membrane-specific capture IgM and IgG ELISA in the differentiation of primary and secondary dengue virus infections showed good correlation (95.90% agreement). Most important, we have found that the serotype of the dengue virus from the majority of patients with primary infection could be correctly identified when convalescent-phase or postinfection sera were analyzed by NS1 serotype-specific IgG ELISA. These findings suggested that NS1 serotype-specific IgG ELISA could be reliably applied for serodiagnosis and seroepidemiological study of dengue virus infection.
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页码:622 / 630
页数:9
相关论文
共 23 条
[1]   Enzyme-linked immunosorbent assay specific to dengue virus type 1 nonstructural protein NS1 reveals circulation of the antigen in the blood during the experiencing primary acute phase of disease in patients or secondary infections [J].
Alcon, S ;
Talarmin, A ;
Debruyne, M ;
Falconar, A ;
Deubel, V ;
Flamand, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (02) :376-381
[2]   WHY DENGUE HEMORRHAGIC-FEVER IN CUBA .1. INDIVIDUAL RISK-FACTORS FOR DENGUE HEMORRHAGIC-FEVER DENGUE SHOCK SYNDROME (DHF DSS) [J].
BRAVO, JR ;
GUZMAN, MG ;
KOURI, GP .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1987, 81 (05) :816-820
[3]   Persistence of Japanese encephalitis virus is associated with abnormal expression of the nonstructural protein NS1 in host cells [J].
Chen, LK ;
Liao, CL ;
Lin, CG ;
Lai, SC ;
Liu, CI ;
Ma, SH ;
Huang, YY ;
Lin, YL .
VIROLOGY, 1996, 217 (01) :220-229
[4]   TECHNIQUES FOR HEMAGGLUTINATION AND HEMAGGLUTINATION-INHIBITION WITH ARTHROPOD-BORNE VIRUSES [J].
CLARKE, DH ;
CASALS, J .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1958, 7 (05) :561-573
[5]   ISOLATION OF PURE IGG1, IGG2A AND IGG2B IMMUNOGLOBULINS FROM MOUSE SERUM USING PROTEIN A-SEPHAROSE [J].
EY, PL ;
PROWSE, SJ ;
JENKIN, CR .
IMMUNOCHEMISTRY, 1978, 15 (07) :429-436
[6]   Evaluation of six immunoassays for detection of dengue virus-specific immunoglobulin M and G antibodies [J].
Groen, J ;
Koraka, P ;
Velzing, J ;
Copra, C ;
Osterhaus, ADME .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2000, 7 (06) :867-871
[7]   EPIDEMIOLOGIC, CLINICAL, AND VIROLOGIC OBSERVATIONS ON DENGUE IN KINGDOM-OF-TONGA [J].
GUBLER, DJ ;
REED, D ;
ROSEN, L ;
HITCHCOCK, JC .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1978, 27 (03) :581-589
[8]  
Gubler DJ, 2014, DENGUE AND DENGUE HEMORRHAGIC FEVER, 2ND EDITION, P1, DOI 10.1079/9781845939649.0001
[9]   STUDIES ON PATHOGENESIS OF DENGUE INFECTION IN MONKEYS .2. CLINICAL LABORATORY RESPONSES TO HETEROLOGOUS INFECTION [J].
HALSTEAD, SB ;
SHOTWELL, H ;
CASALS, J .
JOURNAL OF INFECTIOUS DISEASES, 1973, 128 (01) :15-22
[10]   AN ENZYME-LINKED IMMUNOSORBENT-ASSAY TO CHARACTERIZE DENGUE INFECTIONS WHERE DENGUE AND JAPANESE ENCEPHALITIS CO-CIRCULATE [J].
INNIS, BL ;
NISALAK, A ;
NIMMANNITYA, S ;
KUSALERDCHARIYA, S ;
CHONGSWASDI, V ;
SUNTAYAKORN, S ;
PUTTISRI, P ;
HOKE, CH .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1989, 40 (04) :418-427