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Diagnostic use of polyclonal antibodies raised in mouse ascitic fluid in bancroftian filariasis.

Identifieur interne : 00DA39 ( Main/Exploration ); précédent : 00DA38; suivant : 00DA40

Diagnostic use of polyclonal antibodies raised in mouse ascitic fluid in bancroftian filariasis.

Auteurs : K. Cheirmaraj [Inde] ; M V Reddy ; B C Harinath

Source :

RBID : pubmed:2283388

Descripteurs français

English descriptors

Abstract

Polyclonal antibodies were produced against Brugia malayi adult antigens (BmA (PBS) SAg and BmA (SDS) SAg) in mouse ascitic fluid by immunising Balb/c mice intraperitoneally with high ratio of adjuvant to immunogen. The diagnostic use of these antibodies in detecting circulating filarial antigen in bancroftian filariasis was studied by sandwich enzyme-linked immunosorbent assay (sandwich ELISA) using stick assay system. Both antibodies raised against PBS and SDS soluble antigens were found to be equally sensitive and relatively specific in detection of circulating filarial antigen. When anti BmA (PBS) SAg antibody was used in sandwich ELISA, 90% of microfilaraemic sera, 30-40% of acute and sub acute filarial sera, 20% of chronic filarial sera, 7% of endemic normal sera and none of 15 non-endemic normal sera were positive for filarial antigen. Using anti BmA (SDS) Sag antibody, 93% of microfilarial sera, 40% of acute and sub acute filarial sera, 20% of chronic filarial sera and none of 15 endemic and non-endemic normal sera showed the presence of filarial antigen. The filarial antigen detection using anti BmA S Ag antibodies produced in mouse ascitic fluid in sandwich ELISA may be useful in detection of active stage (microfilaraemia) of infection.

DOI: 10.1080/01971529008055043
PubMed: 2283388


Affiliations:


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<term>Animals</term>
<term>Antibodies, Helminth (isolation & purification)</term>
<term>Antigens, Helminth (blood)</term>
<term>Brugia (immunology)</term>
<term>Elephantiasis, Filarial (diagnosis)</term>
<term>Elephantiasis, Filarial (immunology)</term>
<term>Enzyme-Linked Immunosorbent Assay</term>
<term>Humans</term>
<term>Immunologic Tests</term>
<term>Mice</term>
<term>Microfilariae (immunology)</term>
<term>Wuchereria bancrofti (immunology)</term>
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<term>Animaux</term>
<term>Anticorps antihelminthe (isolement et purification)</term>
<term>Antigènes d'helminthe (sang)</term>
<term>Brugia (immunologie)</term>
<term>Filariose lymphatique (diagnostic)</term>
<term>Filariose lymphatique (immunologie)</term>
<term>Humains</term>
<term>Microfilaria (immunologie)</term>
<term>Souris</term>
<term>Test ELISA</term>
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<div type="abstract" xml:lang="en">Polyclonal antibodies were produced against Brugia malayi adult antigens (BmA (PBS) SAg and BmA (SDS) SAg) in mouse ascitic fluid by immunising Balb/c mice intraperitoneally with high ratio of adjuvant to immunogen. The diagnostic use of these antibodies in detecting circulating filarial antigen in bancroftian filariasis was studied by sandwich enzyme-linked immunosorbent assay (sandwich ELISA) using stick assay system. Both antibodies raised against PBS and SDS soluble antigens were found to be equally sensitive and relatively specific in detection of circulating filarial antigen. When anti BmA (PBS) SAg antibody was used in sandwich ELISA, 90% of microfilaraemic sera, 30-40% of acute and sub acute filarial sera, 20% of chronic filarial sera, 7% of endemic normal sera and none of 15 non-endemic normal sera were positive for filarial antigen. Using anti BmA (SDS) Sag antibody, 93% of microfilarial sera, 40% of acute and sub acute filarial sera, 20% of chronic filarial sera and none of 15 endemic and non-endemic normal sera showed the presence of filarial antigen. The filarial antigen detection using anti BmA S Ag antibodies produced in mouse ascitic fluid in sandwich ELISA may be useful in detection of active stage (microfilaraemia) of infection.</div>
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