Details

Autor(en) / Beteiligte

• Mande, Purvi
• Zirak, Bahar
• Ko, Wei-Che
• Taravati, Keyon
• Bride, Karen L
• Brodeur, Tia Y
• Deng, April
• Dresser, Karen
• Jiang, Zhaozhao
• Ettinger, Rachel
• Fitzgerald, Katherine A
• Rosenblum, Michael D
• Harris, John E
• Marshak-Rothstein, Ann

Titel

Fas ligand promotes an inducible TLR-dependent model of cutaneous lupus-like inflammation

Ist Teil von

• The Journal of clinical investigation, 2018-07, Vol.128 (7), p.2966-2978

Ort / Verlag

United States: American Society for Clinical Investigation

Erscheinungsjahr

2018

Quelle

MEDLINE

Beschreibungen/Notizen

• Toll-like receptors TLR7 and TLR9 are both implicated in the activation of autoreactive B cells and other cell types associated with systemic lupus erythematosus (SLE) pathogenesis. However, Tlr9-/- autoimmune-prone strains paradoxically develop more severe disease. We have now leveraged the negative regulatory role of TLR9 to develop an inducible rapid-onset murine model of systemic autoimmunity that depends on T cell detection of a membrane-bound OVA fusion protein expressed by MHC class II+ cells, expression of TLR7, expression of the type I IFN receptor, and loss of expression of TLR9. These mice are distinguished by a high frequency of OVA-specific Tbet+, IFN-γ+, and FasL-expressing Th1 cells as well as autoantibody-producing B cells. Unexpectedly, contrary to what occurs in most models of SLE, they also developed skin lesions that are very similar to those of human cutaneous lupus erythematosus (CLE) as far as clinical appearance, histological changes, and gene expression. FasL was a key effector mechanism in the skin, as the transfer of FasL-deficient DO11gld T cells completely failed to elicit overt skin lesions. FasL was also upregulated in human CLE biopsies. Overall, our model provides a relevant system for exploring the pathophysiology of CLE as well as the negative regulatory role of TLR9.