IgG4-related disease: A concise review of the current literature

Reumatol Clin. 2017 May-Jun;13(3):160-166. doi: 10.1016/j.reuma.2016.05.009. Epub 2016 Jun 18.
[Article in English, Spanish]

Abstract

IgG4-related disease is the term used to refer to a condition characterized by a lymphoplasmacytic infiltrate, fibrosis and an increased number of IgG4+ cells present in tissue, in most cases, with an elevated serum IgG4 level. This disease frequently affects the pancreas, salivary glands and lymph nodes, but can involve almost any tissue. Its etiology and the exact role of the different inflammatory cells in the damage to the target organ is still unclear. As yet, there is no international consensus about diagnostic criteria for the disease, but there are important advances in its treatment and in the quest to achieve remission. We include a review of the history, possible pathogenesis, clinical manifestations, diagnostic approach and available therapeutic approaches.

Keywords: Autoimmune pancreatitis; Enfermedad de Mikulicz; Enfermedad relacionada con IgG4; IgG4-related disease; Immunoglobulin G4; Inmunoglobulina G4; Mikulicz’ disease; Pancreatitis autoinmune.

Publication types

  • Review

MeSH terms

  • Autoimmune Diseases / diagnosis
  • Autoimmune Diseases / epidemiology
  • Autoimmune Diseases / immunology*
  • Autoimmune Diseases / therapy
  • Biomarkers / metabolism
  • Global Health
  • Humans
  • Immunoglobulin G / metabolism*
  • Incidence
  • Prevalence

Substances

  • Biomarkers
  • Immunoglobulin G