Monoclonal Antibody Based Elisa:An Effective Diagnostic Tool for the Diagnosis of Falciparum Malaria

An enzyme-linked immunosorbent assay (ELISA) system based on the monoclonal antibodies (F2W22C1) originated fromThai strains of P.falciparumin mice models and polyclonal antibodies raised against Nepali strains of P.falciparumin rabbitmodels was developed for the detection of local Nepali strain of...

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Main Author: Hari Har Joshi
Format: Article
Language:English
Published: Nepal Medical Association 2005-07-01
Series:Journal of Nepal Medical Association
Online Access:http://jnma.com.np/jnma/index.php/jnma/article/view/384
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spelling doaj-d617685008764ea0906900dd6a9d28572020-11-24T23:44:16ZengNepal Medical AssociationJournal of Nepal Medical Association0028-27151815-672X2005-07-014415910.31729/jnma.384Monoclonal Antibody Based Elisa:An Effective Diagnostic Tool for the Diagnosis of Falciparum MalariaHari Har Joshi0Kathmandu, Nepal. An enzyme-linked immunosorbent assay (ELISA) system based on the monoclonal antibodies (F2W22C1) originated fromThai strains of P.falciparumin mice models and polyclonal antibodies raised against Nepali strains of P.falciparumin rabbitmodels was developed for the detection of local Nepali strain of P.falciparum antigens in red cell lysates. The monoclonal-polyclonal antibody based indirect ELISA developed for the detection of P.falciparumantigens was specific since it was positive only with P.falciparuminfected erythrocytes and negative when blood fromforty healthy individuals collected fromthe malaria non-endemic areas and forty P.vivax infected erythrocytes were tested. When the test was applied to microscopically confirmed 154 falciparuminfected blood samples collected fromDhanusha district, Nepal; the assay detected only 138 out of 154 P.falciparumsamples indicating the sensitivity of the test to be 89.6%.When the assay was used to detect forty samples from the patients of unknown origin of fever other than the malaria collected fromthe malaria endemic areas, all forty samples were negative with the assay system. A significant correlation was observed (r = 0.872; p = 0.013) in between the parasitemia and the O.D. values obtained fromtheMAb-PAb based indirect ELISA. The test developed using monoclonal antibodies raised against Thai P. falciparum isolates and the polyclonal antibodies raised against native Nepali strains of P.falciparum offered high degrees of sensitivity and specificity. However, the test requires further evaluation with higher number of samples; requires further improvement in sensitivity; before commercial use of the test in patient care. Key Words: ELISA, monoclonal antibodies, polyclonal anti-bodies, P. falciparum. http://jnma.com.np/jnma/index.php/jnma/article/view/384
collection DOAJ
language English
format Article
sources DOAJ
author Hari Har Joshi
spellingShingle Hari Har Joshi
Monoclonal Antibody Based Elisa:An Effective Diagnostic Tool for the Diagnosis of Falciparum Malaria
Journal of Nepal Medical Association
author_facet Hari Har Joshi
author_sort Hari Har Joshi
title Monoclonal Antibody Based Elisa:An Effective Diagnostic Tool for the Diagnosis of Falciparum Malaria
title_short Monoclonal Antibody Based Elisa:An Effective Diagnostic Tool for the Diagnosis of Falciparum Malaria
title_full Monoclonal Antibody Based Elisa:An Effective Diagnostic Tool for the Diagnosis of Falciparum Malaria
title_fullStr Monoclonal Antibody Based Elisa:An Effective Diagnostic Tool for the Diagnosis of Falciparum Malaria
title_full_unstemmed Monoclonal Antibody Based Elisa:An Effective Diagnostic Tool for the Diagnosis of Falciparum Malaria
title_sort monoclonal antibody based elisa:an effective diagnostic tool for the diagnosis of falciparum malaria
publisher Nepal Medical Association
series Journal of Nepal Medical Association
issn 0028-2715
1815-672X
publishDate 2005-07-01
description An enzyme-linked immunosorbent assay (ELISA) system based on the monoclonal antibodies (F2W22C1) originated fromThai strains of P.falciparumin mice models and polyclonal antibodies raised against Nepali strains of P.falciparumin rabbitmodels was developed for the detection of local Nepali strain of P.falciparum antigens in red cell lysates. The monoclonal-polyclonal antibody based indirect ELISA developed for the detection of P.falciparumantigens was specific since it was positive only with P.falciparuminfected erythrocytes and negative when blood fromforty healthy individuals collected fromthe malaria non-endemic areas and forty P.vivax infected erythrocytes were tested. When the test was applied to microscopically confirmed 154 falciparuminfected blood samples collected fromDhanusha district, Nepal; the assay detected only 138 out of 154 P.falciparumsamples indicating the sensitivity of the test to be 89.6%.When the assay was used to detect forty samples from the patients of unknown origin of fever other than the malaria collected fromthe malaria endemic areas, all forty samples were negative with the assay system. A significant correlation was observed (r = 0.872; p = 0.013) in between the parasitemia and the O.D. values obtained fromtheMAb-PAb based indirect ELISA. The test developed using monoclonal antibodies raised against Thai P. falciparum isolates and the polyclonal antibodies raised against native Nepali strains of P.falciparum offered high degrees of sensitivity and specificity. However, the test requires further evaluation with higher number of samples; requires further improvement in sensitivity; before commercial use of the test in patient care. Key Words: ELISA, monoclonal antibodies, polyclonal anti-bodies, P. falciparum.
url http://jnma.com.np/jnma/index.php/jnma/article/view/384
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