An antigen detection assay for diagnosing filariasis

In this study we examined the diagnostic potential of monoclonal antibodies (MAb) reactive to antigens of adult Brugia malayi, their microfilariae and antigen of Dirofilaria immitis. The MAb of clone 17E10, which were of IgM isotype, reacted to the inner cuticles and internal content of both male an...

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Main Authors: Sirichit Wongkamchai, Wej Choochote, Achariya Jitpuckdee, Saravud Suvannadabba, Sumart Loymak, Yuwaporn Sakolvaree, Pramuan Tapchaisri, Wanpen Chaicumpa
Other Authors: Mahidol University
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Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/20867
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spelling th-mahidol.208672018-07-24T10:28:35Z An antigen detection assay for diagnosing filariasis Sirichit Wongkamchai Wej Choochote Achariya Jitpuckdee Saravud Suvannadabba Sumart Loymak Yuwaporn Sakolvaree Pramuan Tapchaisri Wanpen Chaicumpa Mahidol University Chiang Mai University Thailand Ministry of Public Health Phikulthong Royal Development Ctr. Thammasat University Immunology and Microbiology Medicine In this study we examined the diagnostic potential of monoclonal antibodies (MAb) reactive to antigens of adult Brugia malayi, their microfilariae and antigen of Dirofilaria immitis. The MAb of clone 17E10, which were of IgM isotype, reacted to the inner cuticles and internal content of both male and female worms and also to the sheath and internal content of microfilariae in utero. However, these MAb did not react to the sheath of blood circulating microfilariae. The MAb 17E10 produced a smear pattern between 37 to > 200 kDa in the Western blot analysis against a SDS-PAGE separated extract of B. malayi. The epitopes were non-protein in nature as indicated by their resistance to proteinase-K treatment. The MAb 17E10 were applied in a sandwich ELISA to detect filarial antigen in the buffy coat and plasma of patients. We tested patients with different clinical manifestations of brugian filariasis, i.e. microfilaremia (M), lymphangitis (L) and elephantiasis (E), as well as non-symptomatic inhabitants of a filariasis endemic area (NE), and compared them to samples from non-symptomatic inhabitants of disease non-endemic areas (NNE). It was found that 22 of 31 (70.9%) of M, 7 of 13 (53.8%) of L, 2 of 14 (14.2%) of E, 10 of 100 (10.0%) of NE and none (0%) of the NNE were positive for antigenaemia. The assay was also positive in 14 of 15 (93.3%) blood samples from B. malayi microfilaremic cats and in 7 of 7 (100%) blood samples of Dirofilaria immitis microfilaremic dogs. The so-developed test has a high potential for routine diagnosis of active filariasis, for epidemiological studies in both humans and reservoir animals and for monitoring treatment efficacy. 2018-07-24T03:24:10Z 2018-07-24T03:24:10Z 2003-12-01 Article Asian Pacific Journal of Allergy and Immunology. Vol.21, No.4 (2003), 241-251 0125877X 2-s2.0-2942615197 https://repository.li.mahidol.ac.th/handle/123456789/20867 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=2942615197&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Immunology and Microbiology
Medicine
spellingShingle Immunology and Microbiology
Medicine
Sirichit Wongkamchai
Wej Choochote
Achariya Jitpuckdee
Saravud Suvannadabba
Sumart Loymak
Yuwaporn Sakolvaree
Pramuan Tapchaisri
Wanpen Chaicumpa
An antigen detection assay for diagnosing filariasis
description In this study we examined the diagnostic potential of monoclonal antibodies (MAb) reactive to antigens of adult Brugia malayi, their microfilariae and antigen of Dirofilaria immitis. The MAb of clone 17E10, which were of IgM isotype, reacted to the inner cuticles and internal content of both male and female worms and also to the sheath and internal content of microfilariae in utero. However, these MAb did not react to the sheath of blood circulating microfilariae. The MAb 17E10 produced a smear pattern between 37 to > 200 kDa in the Western blot analysis against a SDS-PAGE separated extract of B. malayi. The epitopes were non-protein in nature as indicated by their resistance to proteinase-K treatment. The MAb 17E10 were applied in a sandwich ELISA to detect filarial antigen in the buffy coat and plasma of patients. We tested patients with different clinical manifestations of brugian filariasis, i.e. microfilaremia (M), lymphangitis (L) and elephantiasis (E), as well as non-symptomatic inhabitants of a filariasis endemic area (NE), and compared them to samples from non-symptomatic inhabitants of disease non-endemic areas (NNE). It was found that 22 of 31 (70.9%) of M, 7 of 13 (53.8%) of L, 2 of 14 (14.2%) of E, 10 of 100 (10.0%) of NE and none (0%) of the NNE were positive for antigenaemia. The assay was also positive in 14 of 15 (93.3%) blood samples from B. malayi microfilaremic cats and in 7 of 7 (100%) blood samples of Dirofilaria immitis microfilaremic dogs. The so-developed test has a high potential for routine diagnosis of active filariasis, for epidemiological studies in both humans and reservoir animals and for monitoring treatment efficacy.
author2 Mahidol University
author_facet Mahidol University
Sirichit Wongkamchai
Wej Choochote
Achariya Jitpuckdee
Saravud Suvannadabba
Sumart Loymak
Yuwaporn Sakolvaree
Pramuan Tapchaisri
Wanpen Chaicumpa
format Article
author Sirichit Wongkamchai
Wej Choochote
Achariya Jitpuckdee
Saravud Suvannadabba
Sumart Loymak
Yuwaporn Sakolvaree
Pramuan Tapchaisri
Wanpen Chaicumpa
author_sort Sirichit Wongkamchai
title An antigen detection assay for diagnosing filariasis
title_short An antigen detection assay for diagnosing filariasis
title_full An antigen detection assay for diagnosing filariasis
title_fullStr An antigen detection assay for diagnosing filariasis
title_full_unstemmed An antigen detection assay for diagnosing filariasis
title_sort antigen detection assay for diagnosing filariasis
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/20867
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