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Modulation of Immune Cells as a Therapy for Cutaneous Lupus Erythematosus

Journal

Publisher

MDPI
DOI: 10.3390/ijms231810706

Keywords

cutaneous lupus erythematosus; systemic lupus erythematosus; immune cells; treatments

Funding

  1. FONDECYT [1070352, 1190830, 11200764, 1191300]
  2. FONDEF [D11I1080]
  3. PAI ANID [SA77210051]
  4. Millennium Institute on Immunology and Immunotherapy ANID [ACE 210015, CN09_016/ICN 2021_045]

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CLE is an autoimmune disorder characterized by autoantibody secretion and immune cell recruitment, similar to SLE. It can be divided into different types with varying severity of skin lesions. Type I IFN plays a significant role in the development of CLE. Research aims to develop effective treatments.
Cutaneous lupus erythematosus (CLE) is an autoimmune disorder like systemic lupus erythematosus (SLE). Both SLE and CLE characterize autoantibody secretion and immune cell recruitment. In particular, CLE can be divided into three more frequent types, varying in the severity of the skin lesions they present. The role of type I IFN was shown to be one of the leading causes of the development of this pathology in the skin. Different treatments have been developed and tested against these different variants of CLE to decrease the increasing levels of CLE in humans. In this article, a literature revision discussing the similarities between SLE and CLE is carried out. In addition, new advances in understanding the development of CLE and the leading treatments being evaluated in animal models and clinical trials are reviewed.

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