Literature DB >> 2108093

Induction of interleukin-1 from murine peritoneal macrophages by Pseudomonas aeruginosa exotoxin A.

M L Misfeldt1, P K Legaard, S E Howell, M H Fornella, R D LeGrand.   

Abstract

Pseudomonas exotoxin A, an ADP-ribosylating toxin produced by Pseudomonas aeruginosa, has been shown to stimulate the proliferation of murine thymocytes, which requires the participation of accessory cells. This requirement for accessory cells can be replaced by supernatant from adherent peritoneal exudate cells that have been stimulated with exotoxin A. Antibody to exotoxin A inhibits the induction of the thymocyte mitogenic activity from adherent peritoneal macrophages. However, antibody to exotoxin A had no effect on the thymocyte proliferation if the antibody was added to supernatant which contained thymocyte mitogenic activity. The thymocyte mitogenic activity was associated with a protein or protein complex with a molecular mass of greater than 10,000 daltons. D10 bioassays indicated the presence of interleukin-1 (IL-1) in the supernatant. Antibody to IL-1 inhibited the ability of supernatant to induce thymocytes to proliferate. Therefore, these data suggest that Pseudomonas exotoxin A can stimulate the production of IL-1 from adherent peritoneal cells, which induces murine thymocytes to proliferate.

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Year:  1990        PMID: 2108093      PMCID: PMC258570          DOI: 10.1128/iai.58.4.978-982.1990

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.609


  19 in total

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4.  Biological effects of Pseudomonas aeruginosa exotoxin A: lymphoproliferation of T lymphocytes in athymic mice.

Authors:  P S Holt; M L Misfeldt
Journal:  Eur J Epidemiol       Date:  1988-03       Impact factor: 8.082

Review 5.  T-cell receptor V beta use predicts reactivity and tolerance to Mlsa-encoded antigens.

Authors:  H R MacDonald; R Schneider; R K Lees; R C Howe; H Acha-Orbea; H Festenstein; R M Zinkernagel; H Hengartner
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6.  Variables which affect suppression of the immune response induced by Pseudomonas aeruginosa exotoxin A.

Authors:  P S Holt; M L Misfeldt
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8.  The V beta-specific superantigen staphylococcal enterotoxin B: stimulation of mature T cells and clonal deletion in neonatal mice.

Authors:  J White; A Herman; A M Pullen; R Kubo; J W Kappler; P Marrack
Journal:  Cell       Date:  1989-01-13       Impact factor: 41.582

9.  T cell stimulation by staphylococcal enterotoxins. Clonally variable response and requirement for major histocompatibility complex class II molecules on accessory or target cells.

Authors:  B Fleischer; H Schrezenmeier
Journal:  J Exp Med       Date:  1988-05-01       Impact factor: 14.307

10.  Induction of an immune response in athymic nude mice to thymus-dependent antigens by Pseudomonas aeruginosa exotoxin A.

Authors:  P S Holt; M L Misfeldt
Journal:  Cell Immunol       Date:  1985-10-15       Impact factor: 4.178

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  14 in total

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Authors:  M L Misfeldt
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3.  Altered antigen-presenting capacity of human monocytes after phagocytosis of bacteria.

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4.  Porins of Pseudomonas aeruginosa induce release of tumor necrosis factor alpha and interleukin-6 by human leukocytes.

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5.  Stimulation of innate immunity by susceptible and multidrug-resistant Pseudomonas aeruginosa: an in vitro and in vivo study.

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6.  Dual roles for class II major histocompatibility complex molecules in staphylococcal enterotoxin-induced cytokine production and in vivo toxicity.

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7.  Purified Shiga-like toxins induce expression of proinflammatory cytokines from murine peritoneal macrophages.

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8.  Cytokine response by human monocytes to Clostridium difficile toxin A and toxin B.

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9.  Induction of tumor necrosis factor (TNF) and interleukin-1 (IL-1) by Pseudomonas aeruginosa and exotoxin A-induced suppression of lymphoproliferation and TNF, lymphotoxin, gamma interferon, and IL-1 production in human leukocytes.

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10.  Lymphoproliferative activity of Pseudomonas exotoxin A is dependent on intracellular processing and is associated with the carboxyl-terminal portion.

Authors:  P K Legaard; R D LeGrand; M L Misfeldt
Journal:  Infect Immun       Date:  1992-04       Impact factor: 3.609

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