Abstract
The role of IgG in rapid expulsion of Trichinella spiralis in adult rats was analysed. In this experimental model, rats were first infected with an unrelated nematode Heligmosomoides polygyrus, then 5-14 days later, immune serum, its fractions, or IgG monoclonal antibody (mAb) was transferred. Rats were challenged with T. spiralis muscle larvae 24 hr after antibody transfer and intestinal worms counted at various times, up to 24 hr, after challenge. Provided rats were exposed to H. polygyrus first, immune serum, affinity chromatography-isolated immune IgE, IgE-depleted immune serum, or monoclonal antibodies of IgG1, IgG2a and IgG2c isotypes were all able to transfer rapid expulsion. Protection varied from 40 to greater than 90% larval T. spiralis rejection and was dose dependent, requiring, for IgG1, a minimum of 5 mg of transferred protein. Antibody specificity was predominantly against the dominant larval secreted/cuticular antigen TSL-1 for IgE and was exclusively so for the mAb. A comparison of quantitative differences in effective amounts of transferred antibody as well as the distinct priming requirements suggest that IgE functions through an intestinal mechanism that is different from that for IgG1 and IgG2c. Whether or not IgG2a functions homocytotropically, or as the other IgG has not been resolved. Since neither the T-helper (Th) cell transfer or the H. polygyrus form of intestinal priming confers protection by itself, these data suggest that rapid expulsion is predominantly an antibody-mediated process albeit with a required intestinal element. The results support earlier data in showing that two steps are required for rapid expulsion to be expressed and this is so for both IgE- and IgG-mediated mechanisms. Finally, the results show that IgG of various isotypes and IgE have a functional role in the expression of intestinal immunity.
Full text
PDF







Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Ahmad A., Bell R. G., Wang C. H., Sacuto F. R. Characterization of the thoracic duct T-helper cells that co-mediate, with antibody, the rapid expulsion of Trichinella spiralis in adult rats. Parasite Immunol. 1991 Mar;13(2):147–159. doi: 10.1111/j.1365-3024.1991.tb00271.x. [DOI] [PubMed] [Google Scholar]
- Ahmad A., Wang C. H., Bell R. G. A role for IgE in intestinal immunity. Expression of rapid expulsion of Trichinella spiralis in rats transfused with IgE and thoracic duct lymphocytes. J Immunol. 1991 May 15;146(10):3563–3570. [PubMed] [Google Scholar]
- Ahmad A., Wang C. H., Korenaga M., Bell R. G., Adams L. S. Synergistic interaction between immune serum and thoracic duct cells in the adoptive transfer of rapid expulsion of Trichinella spiralis in adult rats. Exp Parasitol. 1990 Jul;71(1):90–99. doi: 10.1016/0014-4894(90)90011-z. [DOI] [PubMed] [Google Scholar]
- Appleton J. A., McGregor D. D. Characterization of the immune mediator of rapid expulsion of Trichinella spiralis in suckling rats. Immunology. 1987 Nov;62(3):477–484. [PMC free article] [PubMed] [Google Scholar]
- Appleton J. A., McGregor D. D. Life-phase specific induction and expression of rapid expulsion in rats suckling Trichinella spiralis-infected dams. Immunology. 1985 Jun;55(2):225–232. [PMC free article] [PubMed] [Google Scholar]
- Appleton J. A., Schain L. R., McGregor D. D. Rapid expulsion of Trichinella spiralis in suckling rats: mediation by monoclonal antibodies. Immunology. 1988 Nov;65(3):487–492. [PMC free article] [PubMed] [Google Scholar]
- Bell R. G., Adams L. S., Ogden R. W. Intestinal mucus trapping in the rapid expulsion of Trichinella spiralis by rats: induction and expression analyzed by quantitative worm recovery. Infect Immun. 1984 Jul;45(1):267–272. doi: 10.1128/iai.45.1.267-272.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bell R. G., McGregor D. D., Adams L. S. Studies on the inhibition of rapid expulsion of Trichinella spiralis in rats. Int Arch Allergy Appl Immunol. 1982;69(1):73–80. doi: 10.1159/000233149. [DOI] [PubMed] [Google Scholar]
- Bell R. G., McGregor D. D., Despommier D. D. Trichinella spiralis: mediation of the intestinal component of protective immunity in the rat by multiple, phase-specific, antiparasitic responses. Exp Parasitol. 1979 Apr;47(2):140–157. doi: 10.1016/0014-4894(79)90068-7. [DOI] [PubMed] [Google Scholar]
- Bell R. G., McGregor D. D. Requirement for two discrete stimuli for induction of the intestinal rapid expulsion response against Trichinella spiralis in rats. Infect Immun. 1980 Jul;29(1):186–193. doi: 10.1128/iai.29.1.186-193.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- CROSS J. H., Jr The natural resistance of the white rat to Nematospiroides dubius and the effect of cortisone on this resistance. J Parasitol. 1960 Apr;46:175–185. [PubMed] [Google Scholar]
- Capron M., Bazin H., Joseph M., Capron A. Evidence for IgE-dependent cytotoxicity by rat eosinophils. J Immunol. 1981 May;126(5):1764–1768. [PubMed] [Google Scholar]
- Carlisle M. S., McGregor D. D., Appleton J. A. The role of mucus in antibody-mediated rapid expulsion of Trichinella spiralis in suckling rats. Immunology. 1990 May;70(1):126–132. [PMC free article] [PubMed] [Google Scholar]
- Conrad D. H., Studer E., Gervasoni J., Mohanakumar T. Properties of two monoclonal antibodies directed against the Fc and Fab' regions of rat IgE. Int Arch Allergy Appl Immunol. 1983;70(4):352–360. doi: 10.1159/000233347. [DOI] [PubMed] [Google Scholar]
- Crum E. D., Despommier D. D., McGregor D. D. Immunity to Trichinella spiralis. I. Transfer of resistance by two classes of lymphocytes. Immunology. 1977 Dec;33(6):787–795. [PMC free article] [PubMed] [Google Scholar]
- Denkers E. Y., Wassom D. L., Hayes C. E. Characterization of Trichinella spiralis antigens sharing an immunodominant, carbohydrate-associated determinant distinct from phosphorylcholine. Mol Biochem Parasitol. 1990 Jun;41(2):241–249. doi: 10.1016/0166-6851(90)90187-q. [DOI] [PubMed] [Google Scholar]
- Dessein A. J., Parker W. L., James S. L., David J. R. IgE antibody and resistance to infection. I. Selective suppression of the IgE antibody response in rats diminishes the resistance and the eosinophil response to Trichinella spiralis infection. J Exp Med. 1981 Feb 1;153(2):423–436. doi: 10.1084/jem.153.2.423. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gold A. M., Despommier D. D., Buck S. W. Partial characterization of two antigens secreted by L1 larvae of Trichinella spiralis. Mol Biochem Parasitol. 1990 Jun;41(2):187–196. doi: 10.1016/0166-6851(90)90181-k. [DOI] [PubMed] [Google Scholar]
- Isersky C., Kulczycki A., Jr, Metzger H. Isolation of IgE from reaginic rat serum. J Immunol. 1974 May;112(5):1909–1919. [PubMed] [Google Scholar]
- Love R. J., Ogilvie B. M., McLaren D. J. The immune mechanism which expels the intestinal stage of Trichinella spiralis from rats. Immunology. 1976 Jan;30(1):7–15. [PMC free article] [PubMed] [Google Scholar]
- Newlands G. F., Huntley J. F., Miller H. R. Concomitant detection of mucosal mast cells and eosinophils in the intestines of normal and Nippostrongylus-immune rats. A re-evaluation of histochemical and immunocytochemical techniques. Histochemistry. 1984;81(6):585–589. doi: 10.1007/BF00489539. [DOI] [PubMed] [Google Scholar]
- Russell D. A., Castro G. A. Physiological characterization of a biphasic immune response to Trichinella spiralis in the rat. J Infect Dis. 1979 Mar;139(3):304–312. doi: 10.1093/infdis/139.3.304. [DOI] [PubMed] [Google Scholar]
- Springer T. A., Bhattacharya A., Cardoza J. T., Sanchez-Madrid F. Monoclonal antibodies specific for rat IgG1, IgG2a, and IgG2b subclasses, and kappa chain monotypic and allotypic determinants: reagents for use with rat monoclonal antibodies. Hybridoma. 1982;1(3):257–273. doi: 10.1089/hyb.1.1982.1.257. [DOI] [PubMed] [Google Scholar]
- Wang C. H., Korenaga M., Sacuto F. R., Ahmad A., Bell R. G. Intraintestinal migration to the epithelium of protective, dividing, anti-Trichinella spiralis CD4+ OX22- cells requires MHC class II compatibility. J Immunol. 1990 Aug 1;145(3):1021–1028. [PubMed] [Google Scholar]