Fiche publication
Date publication
mars 2017
Journal
Medecine sciences : M/S
Lien Pubmed
Résumé
Autoimmune diseases such as systemic lupus, are the consequence of immunity directed against the organism itself. The immune system abnormally recognizes self-components as foreign and produces antibodies targeting normal cells and tissues. We and others have discovered a number of failures affecting autophagy pathways in the lymphocytes of model mice and patients with lupus. While the current treatments are mainly based on immunosuppressive drugs that can lead to important side effects, the synthetic phosphopeptide P140/Lupuzor, which targets chaperone-mediated autophagy and displays no side effects, holds a lot of promise as a drug candidate. P140, which is currently evaluated in a phase III clinical trial, targets chaperone-mediated autophagy that is hyperactivated in lupus mice, and reduces antigenic peptides presentation to autoreactive helper T cells. Remarkably, we showed in lupus mice that upon treatment with P140, a number of immunological abnormalities affecting the pool of T and B cells as well as many biological and clinical features no longer occur.
Mots clés
Animals, Antigen Presentation, physiology, Autoimmune Diseases, immunology, Autoimmunity, physiology, Autophagy, physiology, B-Lymphocytes, immunology, Disease Models, Animal, Humans, Lupus Erythematosus, Systemic, immunology, Mice
Référence
Med Sci (Paris). 2017 Mar;33(3):319-327
