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Production of a monoclonal antibody specific for ovine immunoglobulin E and its application to monitor serum IgE responses to Haemonchus contortus infection
Part of the Cε3–Cε4 region of the ovine immunoglobulin E (IgE) gene (nucleotides 1111–1575) was amplified by PCR. The recombinant protein (recIgE1-2) was expressed in E. coli and both monoclonal and polyclonal antibodies were produced. These antibodies recognized recIgE1-2 and native IgE on Western...
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Published in: | Parasitology 1997-04, Vol.114 (4), p.395-406 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Part of the Cε3–Cε4 region of the ovine immunoglobulin
E
(IgE) gene (nucleotides 1111–1575) was amplified by PCR.
The recombinant protein (recIgE1-2) was expressed in E. coli and
both
monoclonal and polyclonal antibodies were
produced. These antibodies recognized recIgE1-2 and native IgE on Western
blots
and in ELISA. The polyclonal serum
showed cross-reactivity with other sheep immunoglobulin classes. The monoclonal
antibody was specific for ovine IgE
and goat IgE. Infection of sheep with the abomasal nematode Haemonchus
contortus resulted in elevated IgE levels in
serum 2–4 weeks after infection, as measured by sandwich ELISA using
the
rabbit polyclonal as capture antibody and
the monoclonal antibody against ovine IgE as second antibody. A negative
correlation between worm counts and total
serum IgE levels at the end of the experiment was found in repeatedly infected
sheep. Significant increased levels of
excretory–secretory antigens specific IgE levels were found after
H.
contortus infection. In contrast, no significant changes
in 3rd-stage larvae (L3) antigen-specific IgE titre in sera could be detected
after infection. |
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ISSN: | 0031-1820 1469-8161 |
DOI: | 10.1017/S0031182096008633 |