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Human neurocysticercosis: Comparison of enzyme immunoassay capture techniques based on monoclonal and polyclonal antibodies for the detection of parasite products in cerebrospinal fluid

  • Dolores Correa(corresponding author)
    ,
  • Miguel A. Sandoval
    ,
  • Leslie J.S. Harrison
    ,
  • R. Michael E. Parkhouse
    ,
  • Agustin Plancarte
    ,
  • Antonio Meza-Lucas
*Corresponding author for this work
  • Universidad Nacional Autónoma de México
    ,
  • SSA Mexico
    ,
  • Hospital de Especialidades
    ,
  • University of Edinburgh
    ,
  • Medical Research Council
Research Output:
Contribution to journal
Article
Peer-review

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 814-816 (3 pages)

Journal (Volume, Issue Number)

Transactions of the Royal Society of Tropical Medicine and Hygiene (Volume 83, Issue 6)

Publication milestones

  • Published - 01/12/1989

Publication status

Published - 01/12/1989

ISSN

0035-9203

Publication IDs

  • Scopus: 0024355429
  • PubMed: 2694513

Abstract

Current diagnosis of neurocysticercosis relies mostly on computerized tomography and nuclear magnetic resonance, with detection of antibodies being confirmatory rather than decisive. An assay which detects parasite products in cerebrospinal fluid would conclusively demonstrate a current infection and could be important when decisions regarding treatment must be made. Cerebrospinal fluid from patients with neurocysticercosis was used in 4 enzyme immunoassay capture tests designed to detect parasite products. Of the systems tested, one, based on the use of a monoclonal antibody reactive with a surface and secretion component of the metacestode, was particularly promising, giving a sensitivity of 72%. The assay has the double advantage of a very low background and a proved specificity for the products of living cysticerci. The other 3 systems (monoclonal antivesicular fluid antibody, polyclonal antibody against a saline extract and polyclonal anti-antigen B antibody) were less sensitive. Results with the anti-antigen B system support the proposal that products of low immunogenicity are the most appropriate targets for the serological detection of the parasite.