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Updated: Apr 30, 2026

The bm12 Inducible Model of Systemic Lupus Erythematosus SLE in C57BL/6 Mice
Published on: November 1, 2015
Drug-induced lupus erythematosus
A V Marzano1, S Tavecchio, C Menicanti
1Operative Unit of Dermatology Department of Pathophysiology and Transplantation University of Milan, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy - angelovalerio.marzano@policlinico.mi.it.
Drug-induced lupus erythematosus (DI-LE) mimics idiopathic lupus but resolves after drug withdrawal. DI-SCLE, the most common form, presents with widespread lesions and specific rashes, distinguishing it from other lupus types.
Area of Science:
- Dermatology
- Immunology
- Rheumatology
Background:
- Drug-induced lupus erythematosus (DI-LE) shares clinical and serological features with idiopathic lupus.
- DI-LE is categorized into systemic, subacute cutaneous (SCLE), chronic cutaneous (CCLE), and tumidus forms.
- DI-SCLE is the predominant subtype of drug-induced cutaneous lupus.
Purpose of the Study:
- To investigate the distinct clinical features of drug-induced subacute cutaneous lupus erythematosus (DI-SCLE) compared to its idiopathic counterpart.
- To identify diagnostic hallmarks for DI-SCLE.
Main Methods:
- Comparative analysis of clinical manifestations and immunopathological findings in DI-LE and idiopathic lupus.
- Review of histopathological data for DI-SCLE and other DI-LE variants.
Main Results:
- DI-SCLE frequently presents with widespread annular-polycyclic lesions, often involving the lower legs, unlike idiopathic SCLE.
- Malar rash, bullous, erythema multiforme-like, and vasculitic manifestations are characteristic of DI-SCLE.
- Histopathology, including lichenoid interface dermatitis and tissue eosinophilia, is not a reliable differentiator for DI-SCLE.
Conclusions:
- DI-SCLE exhibits distinct clinical features, notably malar rash and specific cutaneous manifestations, differentiating it from idiopathic SCLE.
- Histological findings are not diagnostic for DI-SCLE.
- Management of DI-LE primarily involves drug cessation, with immunomodulatory agents reserved for refractory cases.
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