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Monogenic autoinflammatory disorders: Conceptual overview, phenotype, and clinical approach

Journal

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
Volume 146, Issue 5, Pages 925-937

Publisher

MOSBY-ELSEVIER
DOI: 10.1016/j.jaci.2020.08.017

Keywords

Autoinflammation; innate immunity; inflammasome; IFN; NF-kappa B

Funding

  1. National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) [2R01AR065538, R01AR075906, R01AR073201, P30AR070253, R21AR076630]
  2. National Heart, Lung, and Blood Institute [R21HL150575]
  3. Fundacion Bechara
  4. Arbuckle Family Fund for Arthritis Research
  5. NIAMS [K08-AR074562]
  6. Rheumatology Research Foundation
  7. Boston Children's Hospital
  8. National Institutes of Health [R01 DK113592, R01 HL140898, R01 R01AI134030]

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Autoinflammatory diseases are conditions in which pathogenic inflammation arises primarily through antigen-independent hyperactivation of immune pathways. First recognized just over 2 decades ago, the autoinflammatory disease spectrum has expanded rapidly to include more than 40 distinct monogenic conditions. Related mechanisms contribute to common conditions such as gout and cardiovascular disease. Here, we review the basic concepts underlying the autoinflammatory revolution'' in the understanding of immune-mediated disease and introduce major categories of monogenic autoinflammatory disorders recognized to date, including inflammasomopathies and other IL-1-related conditions, interferonopathies, and disorders of nuclear factor kappa B and/or aberrant TNF activity. We highlight phenotypic presentation as a reflection of pathogenesis and outline a practical approach to the evaluation of patients with suspected autoinflammation.

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