Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2001 Jan;8(1):174-7.
doi: 10.1128/CDLI.8.1.174-177.2001.

Immunodiagnosis of human fascioliasis by an enzyme-linked immunosorbent assay (ELISA) and a micro-ELISA

Affiliations

Immunodiagnosis of human fascioliasis by an enzyme-linked immunosorbent assay (ELISA) and a micro-ELISA

S Carnevale et al. Clin Diagn Lab Immunol. 2001 Jan.

Abstract

Enzyme-linked immunosorbent assay (ELISA) and micro-ELISA were evaluated for their ability to detect anti-Fasciola hepatica antibodies in humans by using excretory-secretory antigen. The sensitivity of each method was 100%, but the specificity was 100% for ELISA and 97% for micro-ELISA. The micro-ELISA could be used as a screening assay and ELISA could be used as a confirmatory method for the serodiagnosis of human fascioliasis.

PubMed Disclaimer

Figures

FIG. 1
FIG. 1
ELISA absorbances of serum samples using FhESA. (A) Analysis of sera obtained from 100 negative control patients and 22 individuals parasitologically positive for F. hepatica infection. The y axis shows the frequency of absorbance measurements. The vertical dashed line represents the cutoff point, which was calculated as 3.09 SDs from the mean of the seronegative group. (B) Specificity of ELISA using sera from groups of patients with proven infections with Toxoplasma gondii (Tg), Trypanosoma cruzi (Tc), Leishmania spp. (Ls), Plasmodium vivax (Pv), cysticercosis (Ci), hydatid disease (Hi), trichinosis (Tq), toxocariasis (Tx), Schistosoma mansoni (Sm), Ascaris lumbricoides (Al), Ancylostoma duodenale (Ad), Enterobius vermicularis (Ev), Strongyloides stercoralis (Ss), Trichuris trichiura (Tt), Taenia spp. (Ts), Entamoeba histolytica (Eh), Giardia lamblia (Gl), syphilis (Sp), tuberculosis (Tb), anti-hepatitis A virus IgM (HAM), IgG antibodies against hepatitis A virus (HAG), hepatitis B (positive for surface antigen) (HB), and hepatitis C (HC). The dashed horizontal line represents the cutoff point. The individuals are indicated by closed squares.
FIG. 2
FIG. 2
Histogram showing the analysis of positive and negative sera by micro-ELISA with FhESA. The dashed line represents the calculated cutoff point.

Similar articles

Cited by

References

    1. Apt W, Aguilera X, Vega F, Zulantay I, Retamal C, Apt P, Sandoval J. Human fascioliasis in rural areas of Central Chile. Rev Med Chile. 1992;120:621–626. - PubMed
    1. Arjona R, Riancho J, Aguado J, Salesa R, Gonzalez-Macias J. Fascioliasis in developed countries: a review of classic and aberrant forms of the disease. Medicine. 1995;74:13–23. - PubMed
    1. Bjorland J, Byran R T, Strauss W, Hillyer G V, McAuley J B. An outbreak of acute fascioliasis among Aymara Indians in the Bolivian Altiplano. Clin Infect Dis. 1995;21:1228–1233. - PubMed
    1. Bradford M M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976;72:248–254. - PubMed
    1. Bryan R T, Michelson M K. Parasitic infections of the liver and biliary tree. In: Surawicz C, Owen R L, editors. Gastrointestinal and hepatic infections. W. B. Philadelphia, Pa: Saunders Company; 1995. pp. 405–454.

LinkOut - more resources