Quercetin ameliorates XIAP deficiency–associated hyperinflammation

Author:

Chiang Samuel C. C.12,Owsley Erika1,Panchal Neelam34,Chaturvedi Vijaya1,Terrell Catherine E.5,Jordan Michael B.126,Mehta Parinda A.12,Davies Stella M.12,Akeno Nagako1,Booth Claire34,Marsh Rebecca A.12

Affiliation:

1. 1Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH;

2. 2Department of Pediatrics, University of Cincinnati, Cincinnati, OH;

3. 3Molecular and Cellular Immunology, University College London Great Ormond Street Institute of Child Health, London, United Kingdom;

4. 4Department of Paediatric Immunology, Great Ormond Street National Health Service Foundation Trust, London, United Kingdom;

5. 5Division of Experimental Hematology and Cancer Biology, Cincinnati Children’s Hospital, Cincinnati, OH; and

6. 6Division of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH

Abstract

Abstract XIAP (X-linked inhibitor of apoptosis) deficiency is a rare inborn error of immunity. XIAP deficiency causes hyperinflammatory disease manifestations due to dysregulated TNF (tumor necrosis factor)-receptor signaling and NLRP3 (NOD- [nucleotide-binding oligomerization domain], LRR- [leucine-rich repeat] and pyrin domain-containing protein 3) inflammasome function. Safe and effective long-term treatments are needed and are especially important to help prevent the need for high-risk allogeneic hematopoietic cell transplantation. Here we evaluated inflammasome inhibitors as potential therapeutics with a focus on the natural flavonoid antioxidant quercetin. Bone marrow (BM)-derived macrophages were derived from XIAP-deficient or wild-type (WT) mice. Human monocytes were obtained from control or XIAP-deficient patients. Cells were stimulated with TLR (Toll-like receptor) agonists or TNF-α ± inhibitors or quercetin. For in vivo lipopolysaccharide (LPS) challenge experiments, XIAP-deficient or WT mice were fed mouse chow ± supplemental quercetin (50 mg/kg per day exposure) for 7 days followed by a challenge with 10 ng/kg LPS. IL-1β (interleukin-1β) and IL-18 were measured by ELISA (enzyme-linked immunosorbent assay). In murine studies, quercetin prevented IL-1β secretion from XIAP knockout cells following TLR agonists or TNF-α stimulation (P < .05) and strongly reduced constitutive production of IL-18 by both WT and XIAP-deficient cells (P < .05). At 4 hours after in vivo LPS challenge, blood levels of IL-1β and IL-18 were significantly decreased in mice that had received quercetin-supplemented chow (P < .05). In experiments using human cells, quercetin greatly reduced IL-1β secretion by monocytes following TNF-α stimulation (P < .05). Our data suggest that quercetin may be an effective natural therapeutic for the prevention of XIAP deficiency-associated hyperinflammation. Clinical trials, including careful pharmacokinetic and pharmacodynamic studies to ensure that effective levels of quercetin can be obtained, are warranted.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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