The Epidemiology and Clinical Manifestations of Autoimmunity in Selective IgA Deficiency

David D. Odineal, M. Eric Gershwin

Research output: Contribution to journalReview article

6 Scopus citations

Abstract

Selective immunoglobulin A deficiency (SIgAD) is the most common primary immunodeficiency, defined as an isolated deficiency of IgA (less than 0.07 g/L). Although the majority of people born with IgA deficiency lead normal lives without significant pathology, there is nonetheless a significant association of IgA deficiency with mucosal infection, increased risks of atopic disease, and a higher prevalence of autoimmune disease. To explain these phenomena, we have performed an extensive literature review to define the geoepidemiology of IgA deficiency and particularly the relative risks for developing systemic lupus erythematosus, hyperthyroidism, hypothyroidism, type 1 diabetes mellitus, Crohn’s disease, ulcerative colitis, rheumatoid arthritis, juvenile idiopathic arthritis, ankylosing spondylitis, and vitiligo; these diseases have strong data to support an association. We also note weaker associations with scleroderma, celiac disease, autoimmune hepatitis, immune thrombocytopenic purpura, and autoimmune hemolytic anemia. Minimal if any associations are noted with myasthenia gravis, lichen planus, and multiple sclerosis. Finally, more recent data provide clues on the possible immunologic mechanisms that lead to the association of IgA deficiency and autoimmunity; these lessons are important for understanding the etiology of autoimmune disease.

Original languageEnglish (US)
JournalClinical Reviews in Allergy and Immunology
DOIs
StatePublished - Jan 1 2019

Keywords

  • Atopy
  • Autoimmune disease
  • Autoimmunity
  • Autoinflammatory disease
  • Primary immunodeficiency
  • Selective immunoglobulin A deficiency

ASJC Scopus subject areas

  • Immunology and Allergy

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