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Noninvasive Urine Biomarker Lateral Flow Immunoassay for Monitoring Active Onchocerciasis.
Shirey, Ryan J; Globisch, Daniel; Eubanks, Lisa M; Hixon, Mark S; Janda, Kim D.
Affiliation
  • Shirey RJ; Department of Chemistry , The Scripps Research Institute , 10550 North Torrey Pines Road , La Jolla , California 92037 , United States.
  • Globisch D; Department of Immunology, The Skaggs Institute for Chemical Biology, The Worm Institute of Research and Medicine (WIRM) , The Scripps Research Institute , 10550 North Torrey , La Jolla , California 92037 , United States.
  • Eubanks LM; Department of Chemistry , The Scripps Research Institute , 10550 North Torrey Pines Road , La Jolla , California 92037 , United States.
  • Hixon MS; Department of Immunology, The Skaggs Institute for Chemical Biology, The Worm Institute of Research and Medicine (WIRM) , The Scripps Research Institute , 10550 North Torrey , La Jolla , California 92037 , United States.
  • Janda KD; Department of Chemistry , The Scripps Research Institute , 10550 North Torrey Pines Road , La Jolla , California 92037 , United States.
ACS Infect Dis ; 4(10): 1423-1431, 2018 10 12.
Article in En | MEDLINE | ID: mdl-30141624
ABSTRACT
The parasitic disease onchocerciasis is the second leading cause of preventable blindness, afflicting more than 18 million people worldwide. Despite an available treatment, ivermectin, and control efforts by the World Health Organization, onchocerciasis remains a burden in many regions. With an estimated 120 million people living in areas at risk of infection, efforts are now shifting from prevention to surveillance and elimination. The lack of a robust, point-of-care diagnostic for an active Onchocerca infection has been a limiting factor in these efforts. Previously, we reported the discovery of the biomarker N-acetyl-tyramine- O-glucuronide (NATOG) in human urine samples and its ability to track treatment progression between medicated patients relative to placebo; we also established its capability to monitor disease burden in a jird model. NATOG is a human-produced metabolite of tyramine, which itself is produced as a nematode neurotransmitter. The ability of NATOG to distinguish between active and past infection overcomes the limitations of antibody biomarkers and PCR methodologies. Lateral flow immunoassay (LFIA) diagnostics offer the versatility and simplicity to be employed in the field and are inexpensive enough to be utilized in large-scale screening efforts. Herein, we report the development and assessment of a NATOG-based urine LFIA for onchocerciasis, which accurately identified 85% of analyzed patient samples ( N = 27).
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Onchocerciasis / Immunoassay / Tyramine / Onchocerca volvulus / Neglected Diseases Type of study: Clinical_trials / Diagnostic_studies / Prognostic_studies Limits: Animals / Humans Language: En Journal: ACS Infect Dis Year: 2018 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Onchocerciasis / Immunoassay / Tyramine / Onchocerca volvulus / Neglected Diseases Type of study: Clinical_trials / Diagnostic_studies / Prognostic_studies Limits: Animals / Humans Language: En Journal: ACS Infect Dis Year: 2018 Document type: Article Affiliation country: United States
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