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Dot enzyme-linked immunosorbent assay for more reliable staging of patients with Human African trypanosomiasis. | LitMetric

AI Article Synopsis

  • Human African trypanosomiasis (HAT) has two stages, with the second being potentially fatal without treatment, necessitating precise disease staging due to toxic treatments available.
  • Recent research identifies specific antibodies (anti-NF and anti-GalC) in cerebrospinal fluid (CSF) as markers for central nervous system involvement, which can help in staging the disease.
  • A dot enzyme-linked immunosorbent assay (dot-ELISA) to detect these antibodies was tested in Angola and the Central African Republic, achieving 83.2% sensitivity and 100% specificity, making it a promising tool for diagnosing CNS involvement in resource-limited settings.

Article Abstract

Human African trypanosomiasis (HAT) or sleeping sickness is a disease characterized by a hemolymphatic stage 1 followed by a meningoencephalitic stage 2 which is fatal without specific treatment. Furthermore, due to the toxicity of drugs used to treat stage 2 (mainly melarsoprol) accurate staging is required. Actual criteria employed during field surveys are not sensitive enough for precise staging. Antineurofilament (anti-NF) and antigalactocerebrosides (anti-GalC) antibodies have been identified in cerebrospinal fluid (CSF) as potential markers of central nervous system (CNS) involvement. We describe a dot enzyme-linked immunosorbent assay (dot-ELISA) to detect anti-GalC and anti-NF antibodies and its value in staging. NF- and GalC-dotted nitrocellulose strips were first developed in our laboratory. They were then evaluated in Angola and Central African Republic on 140 CSF samples. Compared to our staging criteria (i.e., CSF cell count > or = 20 cells/microl, CSF immunoglobulin M concentration > or = 100 mg/liter, and/or the presence of trypanosomes in the CSF), combined detection of both CSF anti-NF and CSF anti-GalC by dot-ELISA showed 83.2% sensitivity and 100.0% specificity. Dot-ELISA could be a useful test to diagnose CNS involvement in HAT in the less-equipped laboratories or in the field situation and to improve patient treatment.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1234101PMC
http://dx.doi.org/10.1128/JCM.43.9.4789-4795.2005DOI Listing

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