Literature DB >> 5328828

The enhancing effect of the microbial flora on macrophage function and the immune response. A study in germfree mice.

H Bauer, F Paronetto, W A Burns, A Einheber.   

Abstract

The immune response to bacteria and to a soluble protein was compared in germfree and conventionalized mice. Sixty germfree and 59 conventionalized mice received a suspension of killed Serratia marcescens into one front foot-pad and sterile horse ferritin into the other and were sacrificed in groups from 2 hr to 14 days after inoculation. All mice had no pre-existing antibody to either antigen and the flora of the conventionalized mice never contained Serratia. Lymphatic tissue changes and the fate of the antigens were followed in axillary lymph nodes and the spleens by histologic, fluorescent antibody, and autoradiographic techniques after tritiated thymidine injection. Individual serum antibody titers for both antigens were determined at each time period. The cellular and serologic responses were slightly delayed in the germfree mice but later equaled and sometimes exceeded those of the conventional animals. In all animals, lymph nodes draining the site of Serratia injection showed a more vigorous response than those on the ferritin-injected side but the reaction was qualitatively the same for both antigens. All lymph nodes contained the antigens by 2 hr after foot-pad injection. With time, both antigens lost their particulate nature sooner in conventionalized than in germfree macrophages. In the latter, both antigens persisted throughout the study while no longer demonstrable with fluoresceinated antiserum in conventional macrophages after the first week. While phagocytosis is equal in germfree and conventional mice, a greater digestive capacity of macrophages for antigens seems to result from the continuous exposure of conventional animals to the immunologic effects of the microbial flora. Conversely, the lack of substantial antigenic stimulation of lymphatic tissue in germfree animals fails to develop these macrophage functions beyond their basic ability to degrade foreign substances. Although the onset of the immune response is delayed in germfree mice, the relatively prolonged antigen digestion and the presumably slower release of immunogenic antigen fragments result in a more sustained and sometimes greater response than in conventional animals. This modifying effect of the microflora on the function of macrophages during the immune response is independent of previous experience with, or the nature of, the antigen.

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Year:  1966        PMID: 5328828      PMCID: PMC2138179          DOI: 10.1084/jem.123.6.1013

Source DB:  PubMed          Journal:  J Exp Med        ISSN: 0022-1007            Impact factor:   14.307


  31 in total

1.  Fate of attenuated tubercle bacilli (BCG) in germ-free and conventional mice.

Authors:  E SUTER; E M KIRSANOW
Journal:  Nature       Date:  1962-07-28       Impact factor: 49.962

2.  The histophysiology of the antibody response. I. Histogenesis of the plasma cell reaction in rabbit spleen.

Authors:  H L LANGEVOORT
Journal:  Lab Invest       Date:  1963-01       Impact factor: 5.662

3.  In vitro transfer of macrophage RNA to lymph node cells.

Authors:  M FISHMAN; R A HAMMERSTROM; V P BOND
Journal:  Nature       Date:  1963-05-11       Impact factor: 49.962

4.  Genetic control of lymphopoiesis, plasma cell formation, and antibody production.

Authors:  G J NOSSAL
Journal:  Int Rev Exp Pathol       Date:  1962

5.  Studies in experimental eosinophilia. V. Eosinophils in lynph nodes of guinea pigs following primary antigenic stimulation.

Authors:  M LITT
Journal:  Am J Pathol       Date:  1963-05       Impact factor: 4.307

6.  Tissue and cellular changes associated with antibody formation in the rat spleen.

Authors:  C H GUNDERSON; D JURAS; M F LA VIA; R W WISSLER
Journal:  JAMA       Date:  1962-06-23       Impact factor: 56.272

7.  The uptake of tritium-labelled thymidine by lymphoid tissue.

Authors:  J M YOFFEY; W O REINHARDT; N B EVERETT
Journal:  J Anat       Date:  1961-07       Impact factor: 2.610

8.  Autoradiographic observations of plasma cell formation.

Authors:  J C SCHOOLEY
Journal:  J Immunol       Date:  1961-03       Impact factor: 5.422

9.  Agglutinins in sera of laboratory workers exposed to Serratia marcescens.

Authors:  M REITMAN; L S SUTTON; R L ALG; W S MILLER; N H GROSS
Journal:  Proc Soc Exp Biol Med       Date:  1955-06

10.  Micromethods for the study of proteins and antibodies. I. Procedure and general applications of hemagglutination and hemagglutination-inhibition reactions with tannic acid and protein-treated red blood cells.

Authors:  A B STAVITSKY
Journal:  J Immunol       Date:  1954-05       Impact factor: 5.422

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  23 in total

Review 1.  Suppression of the immune response by microorganisms.

Authors:  J H Schwab
Journal:  Bacteriol Rev       Date:  1975-06

2.  Bactericidal activity in conventional or decontaminated mice undergoing GVHD or radiation-induced injury.

Authors:  R I Walker; R J Moon; P F Alm; G D Ledney
Journal:  Experientia       Date:  1976-12-15

3.  The Human Microbiome and the Immune System: An Ever Evolving Understanding.

Authors:  Vanessa Rivera-Amill
Journal:  J Clin Cell Immunol       Date:  2014-11-05

4.  Gnotobiological models and methods in immunology.

Authors:  J Sterzl
Journal:  Folia Microbiol (Praha)       Date:  1979       Impact factor: 2.099

5.  Comparison of peritoneal macrophages from germfree and conventional mice.

Authors:  B Mørland; A I Smievoll; T Midtvedt
Journal:  Infect Immun       Date:  1979-12       Impact factor: 3.441

6.  Lysosomal hydrolases in lymphoid tissue from germ-free and neonatal rats.

Authors:  J R Esterly; A C Standen
Journal:  Experientia       Date:  1971-08

Review 7.  Deciphering interactions between the gut microbiota and the immune system via microbial cultivation and minimal microbiomes.

Authors:  Thomas Clavel; João Carlos Gomes-Neto; Ilias Lagkouvardos; Amanda E Ramer-Tait
Journal:  Immunol Rev       Date:  2017-09       Impact factor: 12.988

8.  Localization of translocating Escherichia coli, Proteus mirabilis, and Enterococcus faecalis within cecal and colonic tissues of monoassociated mice.

Authors:  C L Wells; S L Erlandsen
Journal:  Infect Immun       Date:  1991-12       Impact factor: 3.441

9.  Immunity to experimental renal candidiasis in rats.

Authors:  T J Rogers; E Balish
Journal:  Infect Immun       Date:  1978-02       Impact factor: 3.441

10.  Effect of perorally administered lactobacilli on macrophage activation in mice.

Authors:  G Perdigon; M E de Macias; S Alvarez; G Oliver; A A de Ruiz Holgado
Journal:  Infect Immun       Date:  1986-08       Impact factor: 3.441

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