Mechanism-oriented assessment of isotretinoin in chronic or subacute cutaneous lupus erythematosus.

Abstract

Eight of ten patients with chronic or subacute cutaneous lupus erythematosus completed 16 weeks of oral isotretinoin therapy (80 mg/day). All eight patients noted an excellent clinical response without significant side effects. (Two patients did not return to initial two-week follow-up.) Peripheral blood B- and T-cell counts were unaffected by therapy. Therapy was associated with resolution of routine histopathologic abnormalities, conversion of abnormal lesional direct immunofluorescence microscopy to normal, normalization of the epidermis on electron microscopy, and reduction of all T cells near the dermoepidermal junction without change in ratio of T-helper/inducer cells to T-suppressor/cytotoxic cells. Isotretinoin is a clinically effective short-term therapy for chronic or possibly for subacute cutaneous lupus erythematosus. The primary mechanism of action remains unestablished.

• Authors: R C Newton, J L Jorizzo, A R Solomon Jr, R L Sanchez, J C Daniels, J D Bell, T Cavallo
• Journal: Archives of dermatology (Arch Dermatol) Vol. 122 Issue 2 Pg. 170-6 (Feb 1986) ISSN: 0003-987X [Print] United States
• PMID: 3511858 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Complement C3
• Immunoglobulin G
• Tretinoin
• Fibrin
• Isotretinoin

Topics

• Administration, Oral
• Adult
• Basement Membrane (immunology)
• Chronic Disease
• Complement C3 (analysis)
• Drug Evaluation
• Female
• Fibrin (analysis)
• Fluorescent Antibody Technique
• Humans
• Immunoglobulin G (analysis)
• Isotretinoin
• Lupus Erythematosus, Discoid (drug therapy, immunology, pathology)
• Lymphocytes (classification)
• Male
• Middle Aged
• Skin (pathology, ultrastructure)
• Tretinoin (administration & dosage, therapeutic use)