IgE and IgG2a antibody responses are induced by different antigen groups of the nematode Nippostrongylus brasiliensis in rats
- PMID: 8473018
- PMCID: PMC1421812
IgE and IgG2a antibody responses are induced by different antigen groups of the nematode Nippostrongylus brasiliensis in rats
Abstract
The differences were examined between IgE, IgG1 and IgG2a antibody responses against two kinds of nematode antigens in rats infected with Nippostrongylus brasiliensis. With ELISA studies, remarkable IgE and IgG1 antibody responses were observed against antigens in excretory/secretory products (ES) of N. brasiliensis, whereas the IgG2a antibody response against ES was negligible. On the other hand, antibody response to antigens in an extract of homogenized adult worm (AW) was observed mainly in IgG2a, with little response in IgE or IgG1. Immunohistochemical studies showed that IgE- and IgG1-binding antigens were localized almost exclusively in the subventral glands, a secretory apparatus in N. brasiliensis, while IgG2a-binding antigens were found mainly in the nematode wall along the body cavity. Immunoblot analysis revealed that the major IgE- and IgG1-binding molecules in ES were identical. On the other hand, some, but not all, of the major IgG2a-binding molecules in AW were different from the IgE/IgG1-binding molecules in ES. The findings suggest that the IgE/IgG1 and IgG2a antibody responses in N. brasiliensis-infected rats are induced by different groups of nematode antigens. Thus, it is presumed that the production of each class of antibody might be dependent, at least in part, on the nature of the antigen or antigen-linked molecules.
Similar articles
-
IgE antibody responses induced by transplantation of the nematode Nippostrongylus brasiliensis in rats: a possible role of nematode excretory-secretory product in IgE production.Immunology. 1993 Dec;80(4):541-5. Immunology. 1993. PMID: 8307605 Free PMC article.
-
IgE antibody production in rats against multiple components of excretory-secretory products of the nematode Nippostrongylus brasiliensis.Immunology. 1991 Jan;72(1):104-8. Immunology. 1991. PMID: 1997394 Free PMC article.
-
Low-level infection with the nematode Nippostrongylus brasiliensis induces significant and sustained specific and non-specific IgE antibody responses in rats.Immunology. 1992 Jan;75(1):36-40. Immunology. 1992. PMID: 1537600 Free PMC article.
-
Helminths, allergic disorders and IgE-mediated immune responses: where do we stand?Eur J Immunol. 2007 May;37(5):1170-3. doi: 10.1002/eji.200737314. Eur J Immunol. 2007. PMID: 17447233 Review.
-
Regulation of IgE response by IgE-binding factors.Monogr Allergy. 1983;18:52-60. Monogr Allergy. 1983. PMID: 6227819 Review. No abstract available.
Cited by
-
IgE antibody responses induced by transplantation of the nematode Nippostrongylus brasiliensis in rats: a possible role of nematode excretory-secretory product in IgE production.Immunology. 1993 Dec;80(4):541-5. Immunology. 1993. PMID: 8307605 Free PMC article.
-
Up-regulation of Fas (CD95) and induction of apoptosis in intestinal epithelial cells by nematode-derived molecules.Infect Immun. 2002 Aug;70(8):4002-8. doi: 10.1128/IAI.70.8.4002-4008.2002. Infect Immun. 2002. PMID: 12117905 Free PMC article.
-
Immunization with the RgpA-Kgp proteinase-adhesin complexes of Porphyromonas gingivalis protects against periodontal bone loss in the rat periodontitis model.Infect Immun. 2002 May;70(5):2480-6. doi: 10.1128/IAI.70.5.2480-2486.2002. Infect Immun. 2002. PMID: 11953385 Free PMC article.
-
Dissociation of specific and total IgE antibody responses following repeated low-level infections with Nippostrongylus brasiliensis in rats.Clin Exp Immunol. 1993 Jul;93(1):80-4. doi: 10.1111/j.1365-2249.1993.tb06500.x. Clin Exp Immunol. 1993. PMID: 8324906 Free PMC article.
-
Cysteine protease of the nematode Nippostrongylus brasiliensis preferentially evokes an IgE/IgG1 antibody response in rats.Clin Exp Immunol. 1995 Oct;102(1):71-7. doi: 10.1111/j.1365-2249.1995.tb06638.x. Clin Exp Immunol. 1995. PMID: 7554403 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources