Critical protective role of mast cells in a model of acute septic peritonitis

MAST cells play a detrimental role in IgE-dependent allergic reactions. In contrast, a protective function for mast cells has been proposed on the basis of some worm infection models. No reports exist on the in vivo significance of these cells in bacterial infections 1,2 . Here we use congenitally m...

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Veröffentlicht in:Nature (London) 1996-05, Vol.381 (6577), p.75-77
Hauptverfasser: Echtenacher, Bernd, Männel, Daniela N., Hültner, Lothar
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container_issue 6577
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container_title Nature (London)
container_volume 381
creator Echtenacher, Bernd
Männel, Daniela N.
Hültner, Lothar
description MAST cells play a detrimental role in IgE-dependent allergic reactions. In contrast, a protective function for mast cells has been proposed on the basis of some worm infection models. No reports exist on the in vivo significance of these cells in bacterial infections 1,2 . Here we use congenitally mast-cell-deficient W/W v mice and normal +/+ littermates 3,4 to analyse the role of mast cells in a model of acute septic peritonitis (caecum ligation and puncture (CLP)). Following CLP, W/W v mice showed a significantly increased mortality compared to +/+ mice. The selective reconstitution of W/W v mice with cultured +/+ mast cells substantially protected them from the lethal effects of CLP, whereas an anti-tumour-necrosis-factor (TNF) antibody injected immediately after CLP completely suppressed this protection. Our results reveal a previously unrecognized protective role of mast cells and mast-cell-derived TNF in acute bacterial peritonitis.
doi_str_mv 10.1038/381075a0
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In contrast, a protective function for mast cells has been proposed on the basis of some worm infection models. No reports exist on the in vivo significance of these cells in bacterial infections 1,2 . Here we use congenitally mast-cell-deficient W/W v mice and normal +/+ littermates 3,4 to analyse the role of mast cells in a model of acute septic peritonitis (caecum ligation and puncture (CLP)). Following CLP, W/W v mice showed a significantly increased mortality compared to +/+ mice. The selective reconstitution of W/W v mice with cultured +/+ mast cells substantially protected them from the lethal effects of CLP, whereas an anti-tumour-necrosis-factor (TNF) antibody injected immediately after CLP completely suppressed this protection. Our results reveal a previously unrecognized protective role of mast cells and mast-cell-derived TNF in acute bacterial peritonitis.</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/381075a0</identifier><identifier>PMID: 8609992</identifier><identifier>CODEN: NATUAS</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Acute Disease ; Analysis of the immune response. Humoral and cellular immunity ; Animals ; Antibody production ; Bacteria ; Bacterial diseases ; Biological and medical sciences ; Bone Marrow Cells ; Caecum ; Cells, Cultured ; Cellular biology ; Disease Models, Animal ; Erythrocyte Count ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Hematocrit ; Humanities and Social Sciences ; Immunobiology ; Lethal effects ; letter ; Mast Cells - immunology ; Mast Cells - transplantation ; Mice ; Mice, Inbred C57BL ; multidisciplinary ; Peritonitis - immunology ; Rodents ; Science ; Science (multidisciplinary) ; Sepsis - immunology ; Tumor Necrosis Factor-alpha - pharmacology ; Tumors</subject><ispartof>Nature (London), 1996-05, Vol.381 (6577), p.75-77</ispartof><rights>Springer Nature Limited 1996</rights><rights>1996 INIST-CNRS</rights><rights>Copyright Macmillan Journals Ltd. 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In contrast, a protective function for mast cells has been proposed on the basis of some worm infection models. No reports exist on the in vivo significance of these cells in bacterial infections 1,2 . Here we use congenitally mast-cell-deficient W/W v mice and normal +/+ littermates 3,4 to analyse the role of mast cells in a model of acute septic peritonitis (caecum ligation and puncture (CLP)). Following CLP, W/W v mice showed a significantly increased mortality compared to +/+ mice. The selective reconstitution of W/W v mice with cultured +/+ mast cells substantially protected them from the lethal effects of CLP, whereas an anti-tumour-necrosis-factor (TNF) antibody injected immediately after CLP completely suppressed this protection. Our results reveal a previously unrecognized protective role of mast cells and mast-cell-derived TNF in acute bacterial peritonitis.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>8609992</pmid><doi>10.1038/381075a0</doi><tpages>3</tpages></addata></record>
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subjects Acute Disease
Analysis of the immune response. Humoral and cellular immunity
Animals
Antibody production
Bacteria
Bacterial diseases
Biological and medical sciences
Bone Marrow Cells
Caecum
Cells, Cultured
Cellular biology
Disease Models, Animal
Erythrocyte Count
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Hematocrit
Humanities and Social Sciences
Immunobiology
Lethal effects
letter
Mast Cells - immunology
Mast Cells - transplantation
Mice
Mice, Inbred C57BL
multidisciplinary
Peritonitis - immunology
Rodents
Science
Science (multidisciplinary)
Sepsis - immunology
Tumor Necrosis Factor-alpha - pharmacology
Tumors
title Critical protective role of mast cells in a model of acute septic peritonitis
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