Involvement of lymphocytes in asthma and allergic diseases: a genetic point of view

Curr Opin Allergy Clin Immunol. 2013 Oct;13(5):500-6. doi: 10.1097/ACI.0b013e328364ea3a.

Abstract

Purpose of review: The activation and regulation of lymphocytes play a central role in asthmatic inflammation. It is increasingly recognized that diverse panels of lymphocyte lineages and cytokine profiles are involved in the asthmatic phenotypes. In this review, we discuss the advances in the gene variants associated with the regulation of lymphocytes and relevant cytokines underlying asthma and allergic diseases. We also discuss the current evidence about the epigenetic regulation of lymphocyte differentiation and the interaction with environment.

Recent findings: Many genetic variants in asthma are functionally associated with lymphocytes and relevant cytokines. Interleukin (IL)-2RB is important in the homeostasis of T regulatory cells (Tregs) through effects from IL-2. IL-18R1 and ST2/IL-1RL1 drive the T helper 1 and 2 inflammation via the ligands of their encoding receptors. Novel genes, like orosomucoid 1-like 3/gasdermin-like gene and taste receptor type 2 members are being explored for their roles in T-cell activation. T-cell lineages are epigenetically regulated by de novo methyltransferases, histone methylase, CD44 and microRNA. Environmental factors such as second-hand smoke and ambient air pollution modify Tregs differentiation significantly.

Summary: Plenty of genetic loci of lymphocyte regulation provide us a deeper insight into the asthma pathogenesis. Future challenge is to define genetic drivers in asthma phenotypes to provide therapeutic targets.

Publication types

  • Review

MeSH terms

  • Animals
  • Asthma / genetics
  • Asthma / immunology*
  • Cell Differentiation / genetics
  • Cytokines / genetics*
  • Environmental Exposure / adverse effects
  • Epigenesis, Genetic / genetics
  • Genetic Predisposition to Disease
  • Humans
  • Hypersensitivity / genetics
  • Hypersensitivity / immunology*
  • Lymphocyte Activation / genetics
  • Polymorphism, Genetic
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocytes / immunology*
  • Th1-Th2 Balance

Substances

  • Cytokines