| Literature DB >> 33827978 |
Cassio M Fontes1, Barbara D Lipes2, Jason Liu1, Krystle N Agans3,4, Aiwei Yan2, Patricia Shi2, Daniela F Cruz1, Garrett Kelly1, Kelli M Luginbuhl1, Daniel Y Joh1, Stephanie L Foster3,4, Jacob Heggestad1, Angus Hucknall1, Maiken H Mikkelsen5, Carl F Pieper6, Roarke W Horstmeyer1, Thomas W Geisbert3,4, Michael D Gunn7, Ashutosh Chilkoti8.
Abstract
Ebola virus (EBOV) hemorrhagic fever outbreaks have been challenging to deter due to the lack of health care infrastructure in disease-endemic countries and a corresponding inability to diagnose and contain the disease at an early stage. EBOV vaccines and therapies have improved disease outcomes, but the advent of an affordable, easily accessed, mass-produced rapid diagnostic test (RDT) that matches the performance of more resource-intensive polymerase chain reaction (PCR) assays would be invaluable in containing future outbreaks. Here, we developed and demonstrated the performance of a new ultrasensitive point-of-care immunoassay, the EBOV D4 assay, which targets the secreted glycoprotein of EBOV. The EBOV D4 assay is 1000-fold more sensitive than the U.S. Food and Drug Administration-approved RDTs and detected EBOV infection earlier than PCR in a standard nonhuman primate model. The EBOV D4 assay is suitable for low-resource settings and may facilitate earlier detection, containment, and treatment during outbreaks of the disease.Entities:
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Year: 2021 PMID: 33827978 PMCID: PMC8327926 DOI: 10.1126/scitranslmed.abd9696
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956