Systemic Lupus Erythematosus and Deficiencies of Early Components of the Complement Classical Pathway.

Abstract:

:The complement system plays an important role in the innate and acquired immune response against pathogens. It consists of more than 30 proteins found in soluble form or attached to cell membranes. Most complement proteins circulate in inactive forms and can be sequentially activated by the classical, alternative, or lectin pathways. Biological functions, such as opsonization, removal of apoptotic cells, adjuvant function, activation of B lymphocytes, degranulation of mast cells and basophils, and solubilization and clearance of immune complex and cell lysis, are dependent on complement activation. Although the activation of the complement system is important to avoid infections, it also can contribute to the inflammatory response triggered by immune complex deposition in tissues in autoimmune diseases. Paradoxically, the deficiency of early complement proteins from the classical pathway (CP) is strongly associated with development of systemic lupus erythematous (SLE) - mainly C1q deficiency (93%) and C4 deficiency (75%). The aim of this review is to focus on the deficiencies of early components of the CP (C1q, C1r, C1s, C4, and C2) proteins in SLE patients.

journal_name

Front Immunol

journal_title

Frontiers in immunology

authors

Macedo AC,Isaac L

doi

10.3389/fimmu.2016.00055

subject

Has Abstract

pub_date

2016-02-24 00:00:00

pages

55

issn

1664-3224

journal_volume

7

pub_type

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