Item Type: | Article |
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Title: | Impaired inflammatory responses in the reverse arthus reaction through genetic deletion of the C5a receptor |
Creators Name: | Höpken, U.E., Lu, B., Gerard, N.P. and Gerard, C. |
Abstract: | We recently demonstrated that gene-targeted disruption of the C5a anaphylatoxin receptor prevented lung injury in immune complex-mediated inflammation. In this study, we compare the effect of C5aR deficiency in immune complex-induced inflammation in the peritoneal cavity and skin with the results derived from our immune complex alveolitis model. C5aR- deficient mice exhibit decreased migration of neutrophils and decreased levels of TNF-{alpha} and interleukin 6 in the peritoneal reverse passive Arthus reaction compared to their wild-type littermates. In the reverse passive Arthus reaction in the skin the C5aR was also required for the full expression of neutrophil influx and edema formation; C5aR-deficient mice showed reduced neutrophil migration and microvascular permeability changes. In contrast to our studies in immune complex-induced lung inflammation, C5aR deficiency does not completely prevent injury in the peritoneal cavity and skin. These data indicate a dominant role for the C5aR and its ligand in the reverse passive Arthus reaction in the lung and a synergistic role together with other inflammatory mediators in immune complex-mediated peritonitis and skin injury. |
Keywords: | Anaphylatoxin C5a Receptor, Antibodies, Arthus Reaction, Capillary Permeability, CD Antigens, Cell Count, Complement Receptors, Complement System Proteins, Edema, Fc Receptors, Gene Targeting, Immune Complex Diseases, Immunoglobulin G, Inflammation, Interleukin-6, Knockout Mice, Lung, Neutrophils, Ovalbumin, Peritonitis, Peroxidase, Tumor Necrosis Factor-{alpha}, Animals, Mice |
Source: | Journal of Experimental Medicine |
ISSN: | 0022-1007 |
Publisher: | Rockefeller University Press |
Volume: | 186 |
Number: | 5 |
Page Range: | 749-756 |
Date: | 29 August 1997 |
Official Publication: | https://doi.org/10.1084/jem.186.5.749 |
PubMed: | View item in PubMed |
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