Comparison of Two Commercial ELISA Kits for the Detection of Anti-Dengue IgM for Routine Dengue Diagnosis in Laos

被引:4
|
作者
Lu, Yixiao [1 ,5 ]
Sengvilaipaseuth, Onanong [1 ]
Chanthongthip, Anisone [1 ]
Phonemixay, Ooyanong [1 ]
Vongsouvath, Manivanh [1 ]
Phouminh, Phonelavanh [1 ]
Blacksell, Stuart D. [2 ,3 ]
Newton, Paul N. [1 ,3 ]
Dubot-Peres, Audrey [1 ,3 ,4 ]
机构
[1] Mahosot Hosp, Lao Oxford Mahosot Hosp Wellcome Trust Res Unit L, Microbiol Lab, Viangchan 01000, Laos
[2] Mahidol Univ, Fac Trop Med, Mahidol Oxford Trop Med Res Unit, Bangkok 10400, Thailand
[3] Univ Oxford, Churchill Hosp, Ctr Trop Med & Global Hlth, Nuffield Dept Clin Med, Oxford OX3 7LJ, England
[4] UVE Aix Marseille Univ, Unite Virus Emergents, IRD 190, Inserm 1207,IHU Mediterranee Infect, F-13005 Marseille, France
[5] Nagasaki Univ, Grad Sch Biomed Sci, Dept Publ Hlth Adv Prevent Med, Nagasaki 8528534, Japan
基金
英国惠康基金;
关键词
dengue; MAC-ELISA; serology; Laos; IgM; LINKED-IMMUNOSORBENT-ASSAY; IMMUNOGLOBULIN-M; PATHOGENIC LEPTOSPIRA; TAQMAN ASSAY; TESTS;
D O I
10.3390/tropicalmed4030111
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The endemicity of Dengue virus (DENV) infection remains a major public health problem in Lao PDR. In this study, we compared two commercial anti-dengue IgM ELISA kits, Panbio (R) Dengue IgM Capture ELISA (Panbio Kit, Alere, Waltham, MA, USA) and DEN DetectTM MAC-ELISA (InBios kit, InBios International, Inc., Seattle, WA, USA), in the context of diagnosis of patients admitted to hospital with clinical dengue presentation. Two panels of paired blood samples were tested. Panel A was composed of 54 dengue confirmed patients (by DENV real-time RT-PCR) and 11 non-dengue dengue patients (other infections confirmed by corresponding PCR results). Panel B included 74 patients randomly selected from consecutive patients admitted to Mahosot Hospital in 2008 with suspicion of dengue fever according to WHO criteria. Results from panel A showed significantly better sensitivity for Panbio kit (64.8%; 95%CI: 50.6-77.3%) than for InBios kit (18.5%; 95%CI: 9.3-31.4%) when testing admission sera. Sensitivity was increased for both kits when combining results from admission and convalescent sera. Concordant results were obtained from panel B with fair agreement (kappa = 0.29) between both kits when testing single admission samples, and moderate agreement ( kappa = 0.5) when combining results from admission and convalescent sera.
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页数:10
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