Fc Receptors Initiate the Arthus Reaction: Redefining the Inflammatory Cascade
- 19 August 1994
- journal article
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 265 (5175) , 1095-1098
- https://doi.org/10.1126/science.8066448
Abstract
Antibody-antigen complexes initiate the inflammatory response and are central to the pathogenesis of tissue injury. The classical model for this immunopathological cascade, the Arthus reaction, was reinvestigated with a murine strain deficient in Fc receptor expression. Despite normal inflammatory responses to other stimuli, the inflammatory response to immune complexes was markedly attenuated. These results suggest that immune complex-triggered inflammation is initiated by cell bound Fc receptors and is then amplified by cellular mediators and activated complement. These results redefine the inflammatory cascade and may offer other approaches for the study and treatment of immunological injury.Keywords
This publication has 16 references indexed in Scilit:
- Fc receptors: Rubor reduxCell, 1994
- FcR γ chain deletion results in pleiotrophic effector cell defectsCell, 1994
- Augmentation of reverse arthus reaction by mast cells in mice.Journal of Clinical Investigation, 1991
- Fc ReceptorsAnnual Review of Immunology, 1991
- Molecular Immunobiology of Complement Biosynthesis: A Model of Single-Cell Control of Effector-Inhibitor BalanceAnnual Review of Immunology, 1986
- Complement Ligand-Receptor Interactions that Mediate Biological ResponsesAnnual Review of Immunology, 1983
- Measurement of Cutaneous Inflammation: Estimation of Neutrophil Content with an Enzyme MarkerJournal of Investigative Dermatology, 1982
- THE ROLE OF POLYMORPHONUCLEAR LEUKOCYTES IN THE INITIATION AND CESSATION OF THE ARTHUS VASCULITISThe Journal of Experimental Medicine, 1959
- THE CUTANEOUS REACTION TO SOLUBLE ANTIGEN-ANTIBODY COMPLEXESThe Journal of Experimental Medicine, 1958
- SIMILARITIES IN THE MECHANISMS DETERMINING THE ARTHUS AND SHWARTZMAN PHENOMENAThe Journal of Experimental Medicine, 1951