In systemic lupus erythematosus (SLE), the predominant mechanism by which nuclear antigens become accessible to the immune system involves defective clearance of which cellular process?
- A Necrosis — massive cellular lysis releasing intracellular content
- B Autophagy — excessive self-digestion exposing nuclear material
- C Apoptosis — impaired clearance of apoptotic nuclear debris presenting self-antigens ✓
- D Pyroptosis — caspase-1-mediated inflammatory cell death
Explanation
SLE pathogenesis centrally involves defective apoptotic cell clearance: complement deficiency (especially C1q) impairs opsonization and phagocytic removal of apoptotic bodies, causing secondary necrosis and release of nucleosomal antigens (dsDNA, histones, Ro, La). These activate autoreactive B and T cells that escaped tolerance, generating pathogenic autoantibodies. Anti-dsDNA antibodies form immune complexes deposited in kidneys and vessels. C1q deficiency is the strongest single-gene risk for SLE.
Reference: Robbins & Cotran Pathologic Basis of Disease, 10th ed.
High-yield for: NEET PGINI-CETNExTFMGEUSMLEPLABMRCP
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