Deficiency of C7 with systemic lupus erythematosus: solubilization of immune complexes in complement-deficient sera

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Deficiency of C7 with systemic lupus erythematosus: solubilization of immune complexes in complement-deficient sera

Abstract

References

Familial deficiency of the seventh component of complement associated with recurrent bacteremic infections due to Neisseria

Neisseria meningitidis and Neisseria gonorrhoeae bacteremia associated with C6, C7, or C8 deficiency

Lack of linkage between gene(s) controlling the synthesis of the seventh component of complement and the HLA region on chromosome No. 6 in man

Genetic deficiency of the second component of complement (C2) associated with systemic lupus erythematosus. Relation of the complement abnormality and disease manifestations.

Complement deficiency states

Homozygous C2 deficiency with fulminant lupus erythematosus: severe nephritis via the alternative complement pathway

Inherited deficiency of the seventh component of complement associated with nephritis. Propensity to formation of C56 and related C7-consuming activity

Hereditary C7 deficiency. Diagnosis and HLA studies in a French-Canadian family

Use of C6- and C7-deficient human sera in quantitative hemolytic assays for C6 and C7.

Requirements for the solubilization of immune aggregates by complement. The role of the classical pathway

Familial deficiency of two subunits of the first component of complement. C1r and C1s associated with a lupus erythematosus-like disease

Human deficiency of the eighth component of complement. The requirement of C8 for serum Neisseria gonorrhoeae bactericidal activity

Absence of the sixth component of complement in a patient with repeated episodes of meningococcal meningitis

Absence of the eighth component of complement in association with systemic lupus erythematosus-like disease

Hereditary deficiency of the fifth component of complement in man. I. Clinical, immunochemical, and family studies

A new complement function: solubilization of antigen-antibody aggregates

Hereditary deficiency of the seventh component of complement

Inherited complement deficiencies and systemic lupus erythematosus: an immunogenetic puzzle

Studies on the mechanism of solubilization of immune precipitates by serum

Lupus-erythematosus-like syndrome with a familial defect of complement

Homozygous deficiency of C3 in a patient with repeated infections

Hereditary deficiency of the second component of complement (C'2) in man

The complement system in chronic glomerulonephritis: three newly associated aberrations

Anti-DNA activity in systemic lupus erythematosus. A diagnostic and therapeutic guide

Citations

C7 deficiency and persistent haematuria

Familial deficiency of the seventh component of complement associated with recurrent meningococcal infections.

Inherited deficiency of C8 in a patient with recurrent meningococcal infections: further evidence for a dysfunctional C8 molecule and nonlinkage to the HLA system

Lupus diseases associated with hereditary and acquired deficiencies of complement

Immune-complexes solubilization: effect of antigen-antibody ratio and relative role of alternative and classical complement pathways

Inhibition of complement activation in aged individuals due to increased plasma fibronectin concentration

Polymorphism of the seventh component of complement (C7) in a healthy Caucasian population: an immunoblotting study with neuraminidase-treated samples

Recurrent bacterial infections associated with C3 nephritic factor and hypocomplementemia

Terminal complement component deficiencies and rheumatic disease: development of a rheumatic syndrome and anticomplementary activity in a patient with complete C6 deficiency

SLE-like and sicca symptoms in late component (C9) complement deficiency

Formation of soluble immune complexes by complement in sera of patients with various hypocomplementemic states. Difference between inhibition of immune precipitation and solubilization

Inhibition of complement dependent experimental inflammation in human skin by different heparin fractions

Complement and the direct mediation of immune glomerular injury: a new perspective

Inherited complement component deficiencies in membranoproliferative glomerulonephritis

Molecular defects of the C7 gene in two patients with complement C7 deficiency

Inherited deficiency of the seventh component of complement: studies of C7-consuming activity

Inherited deficiency of the seventh component of complement associated with meningococcal meningitis: lack of serum bactericidal activity against Neisseria meningitidis in a girl with C7 deficiency and HLA studies of a C7-deficient Japanese family

Adult immunodeficiency and rheumatic disease

Complement deficiency and disease

IL-17: a new actor in IFN-driven systemic autoimmune diseases

Functionally active complement proteins C6 and C7 detected in C6- and C7-deficient individuals

C7 deficiency, abnormal platelet aggregation, and rheumatoid arthritis

Complement regulation in innate immunity and the acute-phase response: inhibition of mannan-binding lectin-initiated complement cytolysis by C-reactive protein (CRP).

Combined total deficiency of C7 and C4B with systemic lupus erythematosus (SLE)

Collagenase and collagenolytic activity in human osteoarthritic cartilage

Determination of serum bactericidal activity with the aid of luminous bacteria.

'Gelatinase-like' activity from articular chondrocytes in monolayer culture

Identification of the alpha-gamma subunit of the eighth component of complement (C8) in a patient with systemic lupus erythematosus and absent C8 activity: patients and family studies

An inherited defect in the C3 convertase, C3b,Bb, associated with glomerulonephritis

Related Concepts

Related Feeds

Alternative Complement Pathway

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Hereditary C7 deficiency. Diagnosis and HLA studies in a French-Canadian family

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