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Partial deficiency of the fourth component of human complement (C4) and autoantibody directed against C4 in a patient with SLE.

作者信息

Ripoche J, Fontaine M, Godin M, Hauptmann G, Goetz J

出版信息

Ann Immunol (Paris). 1983 Sep-Oct;134D(2):233-45. doi: 10.1016/s0771-050x(83)80089-8.

DOI:10.1016/s0771-050x(83)80089-8
PMID:6559049
Abstract

The finding of dramatically depressed levels of C4 in a 17-year old patient with severe systemic lupus erythematosus (SLE) prompted a genetic study of her family. This study revealed the existence of a partial C4 deficiency; we found the presence of a C4A3,C4BQo haplotype which was transmitted by the mother to each of her children. This patient possessed, in her serum, an autoantibody with anti-C4 specificity. The immunochemical characterization of this autoantibody revealed that it was IgM and belonged to the immunoconglutinin family. We have studied the effects of this autoantibody on the formation and dissociation kinetics of classical C3-convertase.

摘要

相似文献

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Partial deficiency of the fourth component of human complement (C4) and autoantibody directed against C4 in a patient with SLE.
Ann Immunol (Paris). 1983 Sep-Oct;134D(2):233-45. doi: 10.1016/s0771-050x(83)80089-8.
2
Genetic basis of acquired C4 deficiency.
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Clin Exp Immunol. 2015 Jan;179(1):39-49. doi: 10.1111/cei.12342.
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Family study of the major histocompatibility complex in HLA DR3 negative patients with systemic lupus erythematosus.
HLA DR3阴性系统性红斑狼疮患者主要组织相容性复合体的家系研究
Clin Exp Immunol. 1987 Nov;70(2):364-71.