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Method for detecting circulating Toxocara canis antigen and its application in human serum samples.
1Department of Medical Laboratory Sciences, Faculty of Health Sciences, Kobe Tokiwa University, 2-6-2 Otani-cho, Nagata-ku, Kobe, 653-0838, Japan. sishiyama@kobe-tokiwa.ac.jp
Nepal Medical College Journal : NMCJ
|September 23, 2009
Summary
A new sandwich ELISA method detects circulating Toxocara canis antigen, distinguishing active larval migrans (LM) infections. This diagnostic tool helps differentiate active toxocariasis from past exposure, improving patient management.
Area of Science:
- Veterinary Parasitology
- Immunodiagnostics
- Molecular Biology
Background:
- Current immunodiagnostic methods for larval migrans (LM) detect antibodies, not active infections.
- Distinguishing active toxocariasis from past exposure is crucial for effective patient management.
Purpose of the Study:
- To develop a sensitive and specific sandwich ELISA for detecting circulating Toxocara canis antigen.
- To establish a diagnostic tool for identifying active toxocariasis infections.
Main Methods:
- Production of monoclonal antibodies (MAb) against excretory-secretory (ES) antigen of T. canis.
- Development of a sandwich ELISA using a selected MAb (TCMAb12).
- Testing ELISA specificity against various parasite antigens and sensitivity using a standard curve.
Main Results:
- The developed sandwich ELISA demonstrated high specificity for T. canis antigens.
- The assay achieved a detection limit of 5 ng/ml, indicating sufficient sensitivity for toxocariasis diagnosis.
- In suspected toxocariasis patients, 5 out of 9 serum samples tested positive for circulating antigen, suggesting active infection.
Conclusions:
- The sandwich ELISA is a sensitive and specific method for detecting circulating T. canis antigen.
- This assay can differentiate active toxocariasis from antibody-positive cases without active infection.
- The diagnostic tool aids in understanding the prevalence and active status of toxocariasis.
