Literature DB >> 1675628

Genetic control of serum antibody responses of inbred mice to type 1 and type 2 fimbriae from Actinomyces viscosus T14V.

J Haber1, C M Grinnell, J E Beem, W B Clark.   

Abstract

Antibodies reactive with type 1 and type 2 fimbriae from Actinomyces viscosus T14V specifically inhibit the adherence of A. viscosus T14V to salivary pellicle-coated tooth surfaces and other bacteria, and these antibodies are thought to modulate colonization by this microorganism. These studies were done to determine whether previously noted differences in the antibody responses of inbred mice to type 1 and type 2 fimbriae might be under genetic control. The serum immunoglobulin G (IgG) and IgM antibody responses of inbred, F1 hybrid, and H-2 congenic mice, immunized with A. viscosus T14V cells, were analyzed by enzyme-linked immunosorbent assays for antibodies reactive with A. viscosus T14V whole-cell type 1 and type 2 fimbriae. The results confirmed earlier findings and indicated striking variations in the amounts of IgG anti-type 1 (23-fold) and anti-type 2 (48-fold) fimbria antibodies elicited. The responses of the 17 inbred strains tested showed a relatively continuous distribution from high to low, as well as marked differences in the responses of H-2 and Igh-C identical strain pairs. An analysis of the responses of F1 hybrid and H-2 congenic mice indicated dominance of the low-responder gene(s) and control by H-2-linked genes. Antisera from two high-responder strains inhibited in vitro bacterial adherence to a much greater degree than antisera from a low-responding strain. These data suggest polygenic control of the magnitude of the IgG anti-type 1 and anti-type 2 fimbria antibody responses by H-2-linked genes as well as background genes not associated with H-2 or Igh-C loci.

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Year:  1991        PMID: 1675628      PMCID: PMC258019          DOI: 10.1128/iai.59.7.2364-2369.1991

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  37 in total

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Authors:  K L Holmes; R G Palfree; U Hammerling; H C Morse
Journal:  Proc Natl Acad Sci U S A       Date:  1985-11       Impact factor: 11.205

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Authors:  B P Babbitt; P M Allen; G Matsueda; E Haber; E R Unanue
Journal:  Nature       Date:  1985 Sep 26-Oct 2       Impact factor: 49.962

Review 4.  Role of MHC gene products in immune regulation.

Authors:  B Benacerraf
Journal:  Science       Date:  1981-06-12       Impact factor: 47.728

5.  Analysis of the serum antibody responses to type 1 and type 2 fimbriae in mice immunized with Actinomyces viscosus T14V.

Authors:  J Haber; C Grinnell
Journal:  J Periodontal Res       Date:  1989-03       Impact factor: 4.419

6.  A new mouse cell-surface antigen (Ly-m20) controlled by a gene linked to Mls locus and defined by monoclonal antibodies.

Authors:  S Kimura; N Tada; E Nakayama; Y Liu; U Hämmerling
Journal:  Immunogenetics       Date:  1981       Impact factor: 2.846

7.  Genetic control of the murine immune response to cholera toxin.

Authors:  C O Elson; W Ealding
Journal:  J Immunol       Date:  1985-08       Impact factor: 5.422

8.  Unresponsiveness to a foreign antigen can be caused by self-tolerance.

Authors:  D Vidović; P Matzinger
Journal:  Nature       Date:  1988-11-17       Impact factor: 49.962

9.  Immune responses to complex protein antigens I. MHC control of immune responses to bovine albumin.

Authors:  R L Riley; L D Wilson; R N Germain; D C Benjamin
Journal:  J Immunol       Date:  1982-10       Impact factor: 5.422

10.  Fimbria-specific antibodies detach Escherichia coli from human cells.

Authors:  H Mett; L Kloetzlen; K Vosbeck
Journal:  Infect Immun       Date:  1983-06       Impact factor: 3.441

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  1 in total

1.  Immunization against Porphyromonas gingivalis inhibits progression of experimental periodontitis in nonhuman primates.

Authors:  G R Persson; D Engel; C Whitney; R Darveau; A Weinberg; M Brunsvold; R C Page
Journal:  Infect Immun       Date:  1994-03       Impact factor: 3.441

  1 in total

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