We have generated a murine hybridoma that secretes a monoclonal antibody (mAb) that is highly specific for hemoglobin C (HbC) [a2p,6(A3)Glu-.Lys] and shows no cross reactivity with HbA, HbA,, HbF, HbS, HbE, or Hb O-Arab. Using this antibody, we developed a simple and rapid enzyme linked immunosorben
Antigen-capture enzyme-linked immunosorbent assay for the diagnosis of crimean-congo hemorrhagic fever using a novel monoclonal antibody
✍ Scribed by Masayuki Saijo; Qing Tang; Bawudong Shimayi; Lei Han; Yuzhen Zhang; Muer Asiguma; Dong Tianshu; Akihiko Maeda; Ichiro Kurane; Shigeru Morikawa
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 200 KB
- Volume
- 77
- Category
- Article
- ISSN
- 0146-6615
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✦ Synopsis
Abstract
An antigen‐capture enzyme‐linked immunosorbent assay (ELISA) was developed for the diagnosis of Crimean‐Congo hemorrhagic fever (CCHF) using a novel monoclonal antibody, 1B7, to the recombinant nucleoprotein (rNP) of CCHF virus (CCHFV) Chinese strain 8402. This ELISA detected at least 2 ng/100 μl of CCHFV rNP of 8402 and of the Nigeria strain Ibr 10200, and also detected authentic nucleoproteins (NP) of Chinese strains. Although the sensitivity of the ELISA was lower than that of nested reverse transcription polymerase chain reaction (RT‐PCR), it was able to detect nucleoproteins in acute sera of CCHF patients. The presence of anti‐CCHFV IgG decreased the sensitivity of the ELISA, possibly due to competition with 1B7, and this would tend to limit application of the ELISA. However, the method may be useful for the diagnosis of CCHF patients in the acute stage of illness, especially in laboratories not equipped with RT‐PCR testing capabilities. J. Med. Virol. 77:83–88, 2005. © 2005 Wiley‐Liss, Inc.
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