Literature DB >> 98427

In vitro immune response of spleen cells from mice genetically selected for high or low antibody production.

G Doria, G Agarossi, G Biozzi.   

Abstract

The aim of this study was the identification of the cell type in which genes selected for high or low response to SRBC express their functions. Spleen cells from high (H) and low (L) responder mice were immunized with SRBC in the Mishell and Dutton system. An antibody response of different magnitude was found in cultures of H and L spleen cells, the difference being at least as great as that observed in vivo. This finding under experimental conditions allowing the exclusion of any influence of the animal milieu during the immune response, suggest macrophages, B, and T lymphocytes as possible target cells of gene action. In vitro cell separation and recombination experiments in which spleen cells were immunized with SRBC, TNP-LPS, or TNP-HRBC indicate that the genetic differences between H and L responders brought about by selective breeding are expressed in lymphocytes to greater extent than in macrophages. The role of histoincompatibility in the recombination experiments in unlikely but cannot be excluded. Among lymphocytes, B cells but not helper T cells were found more responsive in cultures of spleen cells from H than from L mice.

Entities:  

Mesh:

Year:  1978        PMID: 98427      PMCID: PMC1457421     

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


  19 in total

1.  Role of macrophages in in vitro induction of T-helper cells.

Authors:  P Erb; M Feldmann
Journal:  Nature       Date:  1975-03-27       Impact factor: 49.962

2.  Effect of carrier priming on antibody avidity in the in vivo and in vitro immune response.

Authors:  G Doria; G Agarossi; D Boraschi; M Antonietta
Journal:  Immunology       Date:  1977-04       Impact factor: 7.397

3.  Studies on immunological paralysis. 8. Pneumococcal polysaccharide tolerance and immunity differences between the Biozzi high and low responder lines of mice.

Authors:  J G Howard; G H Christie; B M Courtenay; G Biozzi
Journal:  Eur J Immunol       Date:  1972-06       Impact factor: 5.532

4.  Stimulation of a T-independent primary anti-hapten response in vitro by TNP-lipopolysaccharide (TNP-LPS).

Authors:  D M Jacobs; D C Morrison
Journal:  J Immunol       Date:  1975-01       Impact factor: 5.422

5.  [Genetic regulation of immunoglobulin synthesis during immune response].

Authors:  G Biozzi; C Stiffel; D Mouton; Y Bouthillier; C Decreusefond
Journal:  Ann Immunol (Paris)       Date:  1974-01

6.  Differences in antigen handling by peritoneal macrophages from the Biozzi high and low responder lines of mice.

Authors:  E Wiener; A Bandieri
Journal:  Eur J Immunol       Date:  1974-07       Impact factor: 5.532

7.  Polygenic regulation of antibody synthesis to sheep erythrocytes in the mouse: a genetic analysis.

Authors:  N Feingold; J Feingold; D Mouton; Y Bouthillier; C Stiffel; G Biozzi
Journal:  Eur J Immunol       Date:  1976-01       Impact factor: 5.532

8.  Cytodynamics of the immune response in two lines of mice genetically selected for "high" and "low" antibody synthesis.

Authors:  G Biozzi; C Stiffel; D Mouton; Y Bouthillier; C Decreusefond
Journal:  J Exp Med       Date:  1972-05-01       Impact factor: 14.307

9.  Nonspecific activation of murine lymphocytes. I. Proliferation and polyclonal activation induced by 2-mercaptoethanol and alpha-thioglycerol.

Authors:  M G Goodman; W O Weigle
Journal:  J Exp Med       Date:  1977-03-01       Impact factor: 14.307

10.  Regulation by the H-2 gene complex of macrophage-lymphoid cell interactions in secondary antibody responses in vitro.

Authors:  C W Pierce; J A Kapp; B Benacerraf
Journal:  J Exp Med       Date:  1976-08-01       Impact factor: 14.307

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