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The PI3Kδ inhibitor parsaclisib ameliorates pathology and reduces autoantibody formation in preclinical models of systemic lupus erythematosus and Sjӧgren's syndrome.
- Source :
-
International immunopharmacology [Int Immunopharmacol] 2021 Sep; Vol. 98, pp. 107904. Date of Electronic Publication: 2021 Jun 29. - Publication Year :
- 2021
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Abstract
- Dysregulation of phosphoinositide 3-kinase δ (PI3Kδ) signaling pathway has been implicated in the pathogenesis of inflammatory and autoimmune diseases. Parsaclisib (INCB050465) represents a potent and selective PI3Kδ inhibitor, which is being clinically investigated for treatment of autoimmune hemolytic anemia and hematological malignancies. We characterized the potential of parsaclisib to ameliorate autoimmune mechanisms implicated in the pathophysiology of systemic lupus erythematosus (SLE) and Sjögren's syndrome (SS). Spontaneous mouse models of SLE and SS were utilized to elucidate the efficacy of orally administered parsaclisib on autoreactive B-cell-mediated antibody-driven disease. Parsaclisib significantly reduced disease symptoms and pathology in three distinct mouse models of SLE. Parsaclisib effectively preserved renal function as measured by glomerular filtration rate, abrogated histopathological evidence of nephritis, modulated discrete immune cell subsets, and decreased anti-dsDNA antibody level. Furthermore, parsaclisib demonstrated efficacy in two spontaneous mouse models of SS. Oral parsaclisib treatment ameliorated the severity of salivary gland inflammation and reduced circulating levels of autoantibodies. Parsaclisib mediated improvement of salivary gland inflammation coincided with reduced B-cell activating cytokine (BAFF) in saliva. Transcriptomic analysis of kidney and salivary gland tissues revealed a downregulation in inflammatory gene expression consistent with PI3Kδ pathway inhibition. Parsaclisib reduced autoreactive B-cells and autoantibody levels, and significantly improved nephritis and salivary gland inflammation. These data provide the scientific rationale for PI3Kδ inhibition as a therapeutic strategy for treatment of B-cell-mediated antibody-driven autoimmune diseases.<br /> (Copyright © 2021. Published by Elsevier B.V.)
- Subjects :
- Animals
B-Lymphocytes drug effects
B-Lymphocytes immunology
Class I Phosphatidylinositol 3-Kinases metabolism
Disease Models, Animal
Humans
Lupus Erythematosus, Systemic blood
Lupus Erythematosus, Systemic immunology
Mice
Pyrazoles therapeutic use
Pyrimidines therapeutic use
Pyrrolidines therapeutic use
Sjogren's Syndrome blood
Sjogren's Syndrome immunology
Autoantibodies blood
Class I Phosphatidylinositol 3-Kinases antagonists & inhibitors
Lupus Erythematosus, Systemic drug therapy
Pyrazoles pharmacology
Pyrimidines pharmacology
Pyrrolidines pharmacology
Sjogren's Syndrome drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1878-1705
- Volume :
- 98
- Database :
- MEDLINE
- Journal :
- International immunopharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 34214886
- Full Text :
- https://doi.org/10.1016/j.intimp.2021.107904