Monogenic Adult-Onset Inborn Errors of Immunity

Front Immunol. 2021 Nov 17:12:753978. doi: 10.3389/fimmu.2021.753978. eCollection 2021.

Abstract

Inborn errors of immunity (IEI) are a heterogenous group of disorders driven by genetic defects that functionally impact the development and/or function of the innate and/or adaptive immune system. The majority of these disorders are thought to have polygenic background. However, the use of next-generation sequencing in patients with IEI has led to an increasing identification of monogenic causes, unravelling the exact pathophysiology of the disease and allowing the development of more targeted treatments. Monogenic IEI are not only seen in a pediatric population but also in adulthood, either due to the lack of awareness preventing childhood diagnosis or due to a delayed onset where (epi)genetic or environmental factors can play a role. In this review, we discuss the mechanisms accounting for adult-onset presentations and provide an overview of monogenic causes associated with adult-onset IEI.

Keywords: adult-onset; autoinflammatory disease; common variable immunodeficiency; genetics; inborn errors of immunity; monogenic; mutation; primary immunodeficiency.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adult
  • Age of Onset
  • Autoimmune Diseases / genetics
  • Common Variable Immunodeficiency / genetics
  • Epigenesis, Genetic
  • Female
  • Gene-Environment Interaction
  • Genetic Association Studies
  • Genetic Predisposition to Disease
  • Hereditary Autoinflammatory Diseases / genetics
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Immunity, Innate / genetics
  • Immunologic Deficiency Syndromes / classification
  • Immunologic Deficiency Syndromes / genetics*
  • Lymphohistiocytosis, Hemophagocytic / genetics
  • Lymphoproliferative Disorders / genetics
  • Male
  • Mosaicism
  • Mutation
  • Severe Combined Immunodeficiency / genetics