Literature DB >> 16557809

Cellular Responses of Mice to Diffusion Chambers I. Reactions to Intraperitoneal Diffusion Chambers Containing Listeria monocytogenes and to Bacteria-Free Chambers.

J W Osebold1, P M Outteridge, L D Pearson, R A Dicapua.   

Abstract

Diffusion chambers made with membranes having a pore size of 0.22 mum were implanted in the peritoneal cavities of mice. Chambers that contained no cells induced splenic lymphoreticular hyperplasia and a proliferation of fibroblasts around the chambers. When the chambers contained the bacterium, Listeria monocytogenes, there was strong and continuous chemotaxis of phagocytic cells to the membrane surface. The tendency to incite fibrosis around the chambers containing bacteria produced a tissue reaction resembling a chronic abscess or granuloma. The important difference from a natural lesion was the prevention of direct parasite-host cell interactions. In studies on the pathogenesis of long persisting host-parasite relationships, one might successfully use diffusion chambers to investigate the role of humoral antimicrobial substances as well as the effects of chronic inflammation, with its local concentration of metabolic products and constituents of phagocytic cells. On the other hand, the presence of diffusion chambers in the tissues is an abnormal situation and changes arising from their presence may complicate the interpretations of some experiments.

Entities:  

Year:  1970        PMID: 16557809      PMCID: PMC415978          DOI: 10.1128/iai.2.2.127-131.1970

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


  14 in total

1.  Adjuvant effect of diffusion chambers on soluble antigens.

Authors:  F L ADLER; M FISHMAN
Journal:  Proc Soc Exp Biol Med       Date:  1962-12

2.  The pathogenesis of staphylococcus infections. I. The use of diffusion chambers in establishing the role of staphylococcus toxins.

Authors:  E D HOUSER; L J BERRY
Journal:  J Infect Dis       Date:  1961 Jul-Aug       Impact factor: 5.226

3.  The application of the diffusion-chamber technique to the study of silicosis.

Authors:  R C CURRAN; E V ROWSELL
Journal:  J Pathol Bacteriol       Date:  1958-10

4.  Growth of normal peritoneal cells in diffusion chambers: a study in cell modulation.

Authors:  E SHELTON; M E RICE
Journal:  Am J Anat       Date:  1959-11

5.  Mutation of Listeria monocytogenes After Prolonged In Vivo Survival in Diffusion Chambers.

Authors:  J W Osebold; P M Outteridge; L D Pearson
Journal:  Infect Immun       Date:  1970-02       Impact factor: 3.441

6.  In vitro antibody synthesis by diffusion chamber cultures of spleen cells. I. Methods and effect of 10,000 r on antibody synthesis.

Authors:  D C Vann; T Makinodan
Journal:  J Immunol       Date:  1969-02       Impact factor: 5.422

7.  Secondary response to bovine serum albumin in diffusion chambers. Stimulation with low doses of antigen.

Authors:  D Sulitzeanu; M Birnbaum
Journal:  Immunology       Date:  1969-08       Impact factor: 7.397

8.  Improved diffusion chamber cultures for cytokinetic analysis of antibody response.

Authors:  P Nettesheim; T Nakinodan; C J Chadwick
Journal:  Immunology       Date:  1966-11       Impact factor: 7.397

9.  Cellular immunity of mice infected with Listeria monocytogenes in diffusion chambers.

Authors:  J W Osebold; R A DiCapua
Journal:  J Bacteriol       Date:  1968-06       Impact factor: 3.490

10.  Passive transfer of transplantation immunity. I. Tritiated lymphoid cells. II. Lymphoid cells in millipore chambers.

Authors:  J S NAJARIAN; J D FELDMAN
Journal:  J Exp Med       Date:  1962-05-01       Impact factor: 14.307

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  3 in total

1.  Purification of a monocytosis-producing activity from Listeria monocytogenes.

Authors:  S B Galsworthy; S M Gurofsky; R G Murray
Journal:  Infect Immun       Date:  1977-02       Impact factor: 3.441

2.  Relationship of antimicrobial cellular immunity to delayed hypersensitivity in Listeriosis.

Authors:  J W Osebold; L D Pearson; N I Medin
Journal:  Infect Immun       Date:  1974-02       Impact factor: 3.441

3.  Pathogenesis of Clostridium botulinum Type A: Study of In Vivo Toxin Release by Implantation of Diffusion Chambers Containing Spores, Vegetative Cells, and Free Toxin.

Authors:  J B Suzuki; R Booth; A Benedik; N Grecz
Journal:  Infect Immun       Date:  1971-05       Impact factor: 3.441

  3 in total

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