Abstract
Due to its importance both in the clearance of pathogens that contribute as rheumatic etiological agents and in the disposal of apoptotic bodies and potential autoimmune initiators, deficiencies of the components of the lectin pathway of complement have been found to increase susceptibility and modulate the severity of most rheumatic disorders. This chapter introduces the general aspects of the structure, function, and genetics of lectin pathway components and summarizes current knowledge of the field regarding rheumatic diseases predisposition and modulation.
MeSH terms
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Arthritis, Rheumatoid / immunology
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Arthritis, Rheumatoid / metabolism*
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Arthritis, Rheumatoid / physiopathology
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Complement Pathway, Mannose-Binding Lectin / immunology*
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Complement System Proteins / immunology
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Complement System Proteins / metabolism
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Humans
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Lupus Erythematosus, Systemic / immunology
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Lupus Erythematosus, Systemic / metabolism*
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Lupus Erythematosus, Systemic / physiopathology
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Mannose-Binding Lectins / chemistry
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Mannose-Binding Lectins / genetics
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Mannose-Binding Lectins / immunology
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Mannose-Binding Lectins / metabolism*
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Polymorphism, Genetic
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Rheumatic Fever / immunology
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Rheumatic Fever / metabolism*
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Rheumatic Fever / physiopathology
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Sjogren's Syndrome / immunology
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Sjogren's Syndrome / metabolism*
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Sjogren's Syndrome / physiopathology
Substances
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Mannose-Binding Lectins
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Complement System Proteins