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在间接免疫荧光试验中使用单克隆抗体快速鉴定登革病毒分离株。

Rapid identification of dengue virus isolates by using monoclonal antibodies in an indirect immunofluorescence assay.

作者信息

Henchal E A, McCown J M, Seguin M C, Gentry M K, Brandt W E

出版信息

Am J Trop Med Hyg. 1983 Jan;32(1):164-9. doi: 10.4269/ajtmh.1983.32.164.

Abstract

Type-specific monoclonal antibodies prepared against the four dengue (DEN) virus serotypes were evaluated for their ability to identify low-passage human and mosquito isolates from Jamaica and West Africa by an indirect immunofluorescence assay. Serotyped human isolates from Jamaican dengue fever patients included 12 DEN-1, two DEN-2, and five DEN-4 viruses. Viruses from West Africa included 84 DEN-2 mosquito strains as well as two DEN-1 and one DEN-2 from humans. Results obtained using the immunofluorescence assay were consistent with virus identifications obtained using the more classical but costly and time-consuming plaque-reduction neutralization test. More viral isolates and higher virus yields were obtained using the C6/36 clone of Aedes albopictus cells rather than LLC-MK2 (monkey kidney) cells. Dengue type-specific monoclonal antibodies detected prototype viral antigens 24-48 hours postinfection in C6/36 cells. This is the first time that monoclonal antibodies have been used to serotype low-passage flavivirus isolates.

摘要

制备了针对四种登革热(DEN)病毒血清型的型特异性单克隆抗体,通过间接免疫荧光试验评估其识别来自牙买加和西非的低传代人源和蚊源病毒分离株的能力。来自牙买加登革热患者的血清型人源分离株包括12株DEN-1、2株DEN-2和5株DEN-4病毒。来自西非的病毒包括84株DEN-2蚊株以及2株人源DEN-1和1株人源DEN-2。使用免疫荧光试验获得的结果与使用更经典但成本高且耗时的蚀斑减少中和试验获得的病毒鉴定结果一致。使用白纹伊蚊细胞的C6/36克隆比LLC-MK2(猴肾)细胞获得了更多的病毒分离株和更高的病毒产量。登革热型特异性单克隆抗体在感染后24至48小时在C6/36细胞中检测到原型病毒抗原。这是首次使用单克隆抗体对低传代黄病毒分离株进行血清分型。

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