Literature DB >> 1977693

The secretory antibody response in milk and bile against fimbriae and LPS in rats monocolonized or immunized in the Peyer's patches with Escherichia coli.

U I Dahlgren1, A E Wold, L A Hanson, T Midtvedt.   

Abstract

The homing of lymphoid cells to mucosa-associated lymphoid tissue is, amongst other factors, influenced by the nature of the antigen used to induce an immune response. To study this phenomenon we have monocolonized rats with a type 1 fimbriated Escherichia coli O6K13H1 strain and compared the secretory antibody response to colonization with the primary and secondary response obtained in rats immunized in the Peyer's patches (PP). Samples were tested with respect to the titres of antibodies against two antigens present on the E. coli strain: O6 lipopolysaccharide (LPS) and type 1 fimbrial antigen. In the primary immunized animals, IgA anti-fimbrial antibodies were mainly seen in milk and IgA anti-LPS antibodies mostly found in bile. In the booster immunized, and in the monocolonized, animals there was a shift of the antibody response towards the bile. Thus anti-fimbrial antibodies appeared in milk at approximately the same or at a lower level than in bile and the IgA anti-LPS antibodies were almost completely absent in the milk. The IgG antibody response of the animals immunized in the PP was primarily confined to milk for both anti-LPS and anti-fimbrial antibodies, while the colonized animals responded with higher levels in bile than in milk. IgM antibodies were only seen in the milk, except in primary immunized animals in which biliary IgM antibodies also were found. The data illustrate that: (i) primary stimulated cells predestined to produce IgA anti-LPS antibodies home mainly to the intestine, while cells predestined to anti-fimbrial antibody production have a greater tendency to populate the mammary gland; (ii) after repeated antigen stimulation and maturation of the immune response the cells are directed from the mammary gland to the intestine. We thus conclude that the nature of the antigen and the stage of lymphocyte maturation influences the homing of the cells and the appearance of various antibodies in different secretions.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 1977693      PMCID: PMC1384319     

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


  20 in total

1.  Lightweight stainless steel systems for rearing germfree animals.

Authors:  B E GUSTAFSSON
Journal:  Ann N Y Acad Sci       Date:  1959-05-08       Impact factor: 5.691

2.  Kinetics of extravasation and redistribution of IgA-specific antibody-containing cells in the intestine.

Authors:  A J Husband
Journal:  J Immunol       Date:  1982-03       Impact factor: 5.422

3.  Cellular determinants of mammary cell-mediated immunity in the rat: kinetics of lymphocyte subset accumulation in the rat mammary gland during pregnancy and lactation.

Authors:  M J Parmely; L S Manning
Journal:  Ann N Y Acad Sci       Date:  1983-06-30       Impact factor: 5.691

4.  Comparative aspects of the hepatobiliary transport of IgA.

Authors:  E Orlans; J V Peppard; A W Payne; B M Fitzharris; B M Mullock; R H Hinton; J G Hall
Journal:  Ann N Y Acad Sci       Date:  1983-06-30       Impact factor: 5.691

5.  Subclass restriction of murine antibodies. III. Antigens that stimulate IgG3 in mice stimulate IgG2c in rats.

Authors:  G P Der Balian; J Slack; B L Clevinger; H Bazin; J M Davie
Journal:  J Exp Med       Date:  1980-07-01       Impact factor: 14.307

6.  Dimeric IgA in the rat is transferred from serum into bile but not into milk.

Authors:  U Dahlgren; S Ahlstedt; L Hedman; C Wadsworth; L A Hanson
Journal:  Scand J Immunol       Date:  1981-07       Impact factor: 3.487

7.  Local production of IgG4 in human colostrum.

Authors:  M A Keller; D C Heiner; R M Kidd; A S Myers
Journal:  J Immunol       Date:  1983-04       Impact factor: 5.422

8.  IgA antibodies in rat bile are not solely derived from thoracic duct lymph.

Authors:  U Dahlgren; S Ahlstedt; T Andersson; L Hedman; L A Hanson
Journal:  Scand J Immunol       Date:  1983-06       Impact factor: 3.487

9.  Subclass restriction of murine antibodies. II. The IgG plaque-forming cell response to thymus-independent type 1 and type 2 antigens in normal mice and mice expressing an X-linked immunodeficiency.

Authors:  J Slack; G P Der-Balian; M Nahm; J M Davie
Journal:  J Exp Med       Date:  1980-04-01       Impact factor: 14.307

10.  Peyer's patches: an enriched source of precursors for IgA-producing immunocytes in the rabbit.

Authors:  S W Craig; J J Cebra
Journal:  J Exp Med       Date:  1971-07-01       Impact factor: 14.307

View more
  2 in total

Review 1.  Antibodies in milk.

Authors:  E Telemo; L A Hanson
Journal:  J Mammary Gland Biol Neoplasia       Date:  1996-07       Impact factor: 2.673

2.  Intestinal immunisation with Escherichia coli protects rats against Escherichia coli induced cholangitis.

Authors:  B D Aagaard; M F Heyworth; A L Oesterle; A L Jones; L W Way
Journal:  Gut       Date:  1996-07       Impact factor: 23.059

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.