Dysregulated CD46 shedding interferes with Th1-contraction in systemic lupus erythematosus
| Autor: | Ellinghaus, Ursula, Cortini, Andrea, Pinder, Christopher L., Le Friec, Gaelle, Kemper, Claudia, Vyse, Timothy J. |
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| Jazyk: | angličtina |
| Rok vydání: | 2017 |
| Předmět: |
Adult
Male T-Lymphocytes viruses Immunology Complement Autoimmunity Matrix Metalloproteinase Inhibitors Th1 ACTIVATION Membrane Cofactor Protein Clinical Journal Article Humans Lupus Erythematosus Systemic NOTCH PATHWAY CD46 Complement Activation Research Articles ELEVATED SERUM Innate immunity B-Lymphocytes Science & Technology IFN-GAMMA Research Article|Clinical T cell MULTIPLE-SCLEROSIS Th1 Cells Immunity Innate female genital diseases and pregnancy complications Interleukin-10 Immunodeficiencies and autoimmunity Matrix Metalloproteinase 9 1107 Immunology T-CELLS Female Life Sciences & Biomedicine RESPONSES Signal Transduction |
| Zdroj: | Ellinghaus, U, Cortini, A, Pinder, C L, Le Friec, G, Kemper, C & Vyse, T J 2017, ' Dysregulated CD46 shedding interferes with Th1-contraction in systemic lupus erythematosus ', European Journal of Immunology, vol. 47, no. 7, pp. 1200-1210 . https://doi.org/10.1002/eji.201646822 European Journal of Immunology |
| DOI: | 10.1002/eji.201646822 |
| Popis: | IFN-γ-producing T helper 1 (Th1) cell responses mediate protection against infections but uncontrolled Th1 activity also contributes to a broad range of autoimmune diseases. Autocrine complement activation has recently emerged as key in the induction and contraction of human Th1 immunity: Activation of the complement regulator CD46 and the C3aR expressed by CD4(+) T cells via autocrine generated ligands C3b and C3a, respectively, are critical to IFN-γ production. Further, CD46-mediated signals also induce co-expression of immunosuppressive IL-10 in Th1 cells and transition into a (self)-regulating and contracting phase. In consequence, C3 or CD46-deficient patients suffer from recurrent infections while dysregulation of CD46 signalling contributes to Th1 hyperactivity in rheumatoid arthritis and multiple sclerosis. Here, we report a defect in CD46-regulated Th1 contraction in patients with systemic lupus erythematosus (SLE). We observed that MMP-9-mediated increased shedding of soluble CD46 by Th1 cells was associated with this defect and that inhibition of MMP-9 activity normalized release of soluble CD46 and restored Th1 contraction in patients' T cells. These data may deliver the first mechanistic explanation for the increased serum CD46 levels observed in SLE patients and indicate that targeting CD46-cleaving proteases could be a novel avenue to modulate Th1 responses. This article is protected by copyright. All rights reserved. |
| Databáze: | OpenAIRE |
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