ArticleImmunology1992
Low-level infection with the nematode Nippostrongylus brasiliensis induces significant and sustained specific and non-specific IgE antibody responses in rats.
Article in Immunology, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed.
- Examination of Horizontal Transmission ofJournal of the American Association for Laboratory Animal Science : JAALAS · 2023Article
- Article
- Effects of treatment on IgE responses against parasite allergen-like proteins and immunity to reinfection in childhood schistosome and hookworm coinfections.Infection and immunity · 2013Article
- Social transfer of pathogenic fungus promotes active immunisation in ant colonies.PLoS biology · 2012Article
- Suppression of gamma interferon transcription and production by nematode excretory-secretory antigen during polyclonal stimulation of rat lymph node T cells.Infection and immunity · 2000Article
- Antigen dose-dependent predominance of either direct or sequential switch in IgE antibody responses.Immunology · 1997Article
- Role of T lymphocytes in secretory response to an enteric nematode parasite. Studies in athymic rats.Digestive diseases and sciences · 1995Article
- Article
- Article
- Intestinal epithelial function: the case for immunophysiological regulation. Implications for disease (2).Digestive diseases and sciences · 1993Review
- Dissociation of specific and total IgE antibody responses following repeated low-level infections with Nippostrongylus brasiliensis in rats.Clinical and experimental immunology · 1993Article
Corrections and comments
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Authors and funding
4 authors.
Funding
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Abstract
Specific and non-specific IgE antibody responses were studied in SD rats infected with between 5 and 2500 Nippostrongylus brasiliensis (NB) larvae. In rats with 2500 NB larvae, specific IgE antibody, measured by enzyme-linked immunosorbent assay (ELISA) using NB excretory/secretory substance as antigen, reached a peak at 4 weeks of infection and gradually declined. On the other hand, in rats infected with 10 or 100 NB larvae, specific IgE was induced at 4 weeks of infection and the level continued to rise until at least 8 weeks after infection. The level at 8 weeks was significantly higher in rats infected with 10 or 100 larvae than in rats infected with 2500 larvae. The results indicate that the low-level infection induced a much more sustained specific IgE response than that induced after heavy infection. However, the level of specific IgG was correlated with the dose of infection, and reached a plateau 6 weeks after infection. Total serum IgE increased significantly even in rats infected with five larvae, a dose which did not induce detectable specific IgE. The kinetics of the production of total IgE was different in rats with light and heavy infections. In rats infected with five or 10 larvae, total IgE increased slowly and reached a plateau 4 weeks after infection. On the other hand, rats infected with more than 500 larvae showed a remarkable rise in total IgE at 2 weeks of infection; this rise gradually declined thereafter. Six weeks after infection, total IgE levels were almost the same (2-3 micrograms/ml) in rats infected with 10-2500 NB larvae. These results show that low-level NB infection induces a significant and sustained specific and non-specific IgE response in rats.
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Identifiers
1537600PMC1384799What OpenQuestion holds
Registered trials
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