Literature DB >> 7275179

Adoptive transfer of total and parasite-specific IgE responses in rats infected with Nippostrongylus brasiliensis.

Y Nawa, H R Miller, E Hall, E E Jarrett.   

Abstract

Infection of rats with Nippostrongylus brasiliensis has both a parasite-specific and non-specific IgE stimulating effect. Both these responses can be adoptively transferred with thoracic duct lymphocytes (TDL) from infected rats. The character of the IgE response in the recipient rats was related to the stage after infection of the cell donors. TDL from hyperimmune rats adoptively transferred high serum titres of parasite-specific IgE to infected recipient rats and substantially increased the levels of total IgE. However, adoptive immunization with TDL from donors infected 10 days previously did not stimulate parasite-specific IgE and only slightly increased total IgE levels. After cell fractionation the sIg- cells from day 10 TDL increased the level of total IgE but not parasite-specific IgE whereas sIg- cells from hyperimmune TDL did not induce any IgE response unless given with sIg+ cells. The possible reasons for this are discussed.

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Year:  1981        PMID: 7275179      PMCID: PMC1555133     

Source DB:  PubMed          Journal:  Immunology        ISSN: 0019-2805            Impact factor:   7.397


  13 in total

1.  IgE formation in the rat after infection with Nippostrongylus brasiliensis. II. Proliferation of IgE-bearing cells in neonatally thymectomized animals.

Authors:  J F Urban; T Ishizaka; K Ishizaka
Journal:  J Immunol       Date:  1977-06       Impact factor: 5.422

Review 2.  Stimuli for the production and control of IgE in rats.

Authors:  E E Jarrett
Journal:  Immunol Rev       Date:  1978       Impact factor: 12.988

3.  Elevation of total serum IgE in rats following helminth parasite infection.

Authors:  E Jarrett; H Bazin
Journal:  Nature       Date:  1974-10-18       Impact factor: 49.962

4.  Effect of T cell depletion on the potentiated reagin response.

Authors:  E Jarrett; A Ferguson
Journal:  Nature       Date:  1974-08-02       Impact factor: 49.962

5.  Three classes and four (sub)classes of rat immunoglobulins: IgM, IgA, IgE and IgG1, IgG2a, IgG2b, IgG2c.

Authors:  H Bazin; A Beckers; P Querinjean
Journal:  Eur J Immunol       Date:  1974-01       Impact factor: 5.532

6.  Nature of cells binding anti-IgE in rats immunized with Nippostrongylus brasiliensis: IgE synthesis in regional nodes and concentration in mucosal mast cells.

Authors:  G Mayrhofer; H Bazin; J L Gowans
Journal:  Eur J Immunol       Date:  1976-08       Impact factor: 5.532

7.  Adoptive transfer of the intestinal mast cell response in rats infected with Nippostrongylus brasiliensis.

Authors:  Y Nawa; H R Miller
Journal:  Cell Immunol       Date:  1979-02       Impact factor: 4.868

8.  The protective capacities of fractionated immune thoracic duct lymphocytes against Nippostrongylus brasiliensis.

Authors:  Y Nawa; C R Parish; H R Miller
Journal:  Cell Immunol       Date:  1978-04       Impact factor: 4.868

9.  Protection against Nippostrongylus brasiliensis by adoptive immunization with immune thoracic duct lymphocytes.

Authors:  Y Nawa; H R Miller
Journal:  Cell Immunol       Date:  1978-04       Impact factor: 4.868

10.  Time course studies on rat IgE production in N. Brasiliensis infection.

Authors:  E E Jarrett; D M Haig
Journal:  Clin Exp Immunol       Date:  1976-05       Impact factor: 4.330

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  11 in total

1.  Extract of Nippostrongylus brasiliensis stimulates polyclonal type-2 immunoglobulin response by inducing De novo class switch.

Authors:  H N Ehigiator; A W Stadnyk; T D Lee
Journal:  Infect Immun       Date:  2000-09       Impact factor: 3.441

2.  Modulation of B-cell proliferative response by a soluble extract of Nippostrongylus brasiliensis.

Authors:  H N Ehigiator; A W Stadnyk; T D Lee
Journal:  Infect Immun       Date:  2000-11       Impact factor: 3.441

3.  Basal secretion and anaphylactic release of rat mast cell protease-II (RMCP-II) from ex vivo perfused rat jejunum: translocation of RMCP-II into the gut lumen and its relation to mucosal histology.

Authors:  C L Scudamore; A M Pennington; E Thornton; L McMillan; G F Newlands; H R Miller
Journal:  Gut       Date:  1995-08       Impact factor: 23.059

4.  Effect of cyclosporin A on rat mucosal mast cells and the associated protease RMCPII.

Authors:  A G Cummins; G H Munro; A Ferguson
Journal:  Clin Exp Immunol       Date:  1988-04       Impact factor: 4.330

5.  Anaphylactic release of mucosal mast cell protease and its relationship to gut permeability in Nippostrongylus-primed rats.

Authors:  S J King; H R Miller
Journal:  Immunology       Date:  1984-04       Impact factor: 7.397

6.  Mucosal damage during intestinal anaphylaxis in the rat. Effect of betamethasone and disodium cromoglycate.

Authors:  R D'Incà; R H Hunt; M H Perdue
Journal:  Dig Dis Sci       Date:  1992-11       Impact factor: 3.199

7.  Systemic release of mucosal mast-cell protease in primed rats challenged with Nippostrongylus brasiliensis.

Authors:  H R Miller; R G Woodbury; J F Huntley; G Newlands
Journal:  Immunology       Date:  1983-07       Impact factor: 7.397

8.  Depletion of mucosal mast cell protease by corticosteroids: effect on intestinal anaphylaxis in the rat.

Authors:  S J King; H R Miller; G F Newlands; R G Woodbury
Journal:  Proc Natl Acad Sci U S A       Date:  1985-02       Impact factor: 11.205

9.  Type 2 cytokine responses: regulating immunity to helminth parasites and allergic inflammation.

Authors:  Everett K Henry; Juan M Inclan-Rico; Mark C Siracusa
Journal:  Curr Pharmacol Rep       Date:  2017-10-19

10.  Release of the mucosal mast cell granule chymase, rat mast cell protease-II, during anaphylaxis is associated with the rapid development of paracellular permeability to macromolecules in rat jejunum.

Authors:  C L Scudamore; E M Thornton; L McMillan; G F Newlands; H R Miller
Journal:  J Exp Med       Date:  1995-12-01       Impact factor: 14.307

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