1. Development and evaluation of an antigen targeting lateral flow test for Crimean-Congo Haemorrhagic Fever.
- Author
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Thompson CR, Bozkurt I, Cosgun Y, Blundell P, Duvoix A, Johnson M, Hedef H, Arslan FG, Umudum BA, Bilek HC, Tanyel E, Pektaş AN, Taşseten TN, Bakir M, Büyüktuna SA, Olçar Y, Yilmaz FA, Arslan M, Al-Hilfi RA, Hasan HA, Khaleel RI, Aufi IM, Mahdi SG, Aakef IR, Shakir HA, Hussein AA, Abdulhadi NA, Mohsin ZA, Korukluoglu G, Cubas Atienzar AI, Fletcher TE, and Adams E
- Subjects
- Humans, Male, Female, Retrospective Studies, Prospective Studies, Diagnostic Tests, Routine methods, Middle Aged, Chromatography, Affinity methods, Adult, Hemorrhagic Fever, Crimean diagnosis, Hemorrhagic Fever Virus, Crimean-Congo immunology, Hemorrhagic Fever Virus, Crimean-Congo genetics, Sensitivity and Specificity, Antigens, Viral immunology
- Abstract
Background: Crimean-Congo Haemorrhagic Fever (CCHF) is a viral haemorrhagic fever with a case fatality rate of 5-25% that has been prioritised for research and development by the World Health Organisation. There are no CCHF rapid diagnostic tests (RDTs) commercially available. We describe the development and evaluation of an antigen-targeting lateral flow immunoassay RDT for CCHF., Methods: Prospective clinical samples were collected and tested between July and October 2023 in Türkiye. Retrospective stored samples were obtained from the Central Public Health Laboratory, Baghdad, Iraq. The sensitivity and specificity of the CCHF RDT was compared to reverse transcription quantitative polymerase chain reaction assays., Findings: On prospective clinical samples in Türkiye, the sensitivity and specificity of the CCHF RDT was 90.4% [95% CI 81.5-95.3%] (n = 73) and 96.2% [95% CI 87.0-99.3%] (n = 52), respectively with a sensitivity of 92.9% [95% CI 84.3-96.9%] (n = 70) in samples with a cycle threshold (Ct) ≤30. On retrospective stored samples in Iraq, sensitivity and specificity of the RDT was 71.7% [95% CI 59.2-81.5%] (n = 60) and 92.5% [95% CI 80.1-97.8%] (n = 40), respectively with a sensitivity of 82.2% [95% CI 68.7-90.7%] (n = 45) in samples of Ct ≤30., Interpretation: The CCHF RDT was an effective rapid diagnostic test in this preliminary clinical evaluation, showing this RDT has the potential diagnostic capability for use at the point-of-care. Definitive evaluation is now required to ensure the RDT meets the regulatory requirements for commercialisation., Funding: The Liverpool School of Tropical Medicine, National Institute for Health Research Health Protection Research Unit in Emerging Zoonotic Infections, The Medical Research Council and The Pandemic Institute., Competing Interests: Declaration of interests LSTM intends to out-license the antibodies to facilitate the future commercialisation of the rapid diagnostic test (RDT). Additionally, we are evaluating the potential for filing a patent application for the antibodies. EA collects salary from the Liverpool School of Tropical Medicine and Global Access Diagnostics., (Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.)
- Published
- 2024
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