Programming of the lung in early life by bacterial infections predisposes to chronic respiratory disease

Clin Obstet Gynecol. 2013 Sep;56(3):566-76. doi: 10.1097/GRF.0b013e3182993a0c.

Abstract

There is emerging evidence that chronic respiratory diseases such as asthma and emphysema may originate in early life. Respiratory infections with certain bacterial pathogens such as Chlamydia, Haemophilus influenzae and Streptococcus pneumoniae in early life may promote permanent deleterious changes in immunity, lung structure, and function that predispose to, or increase the severity of chronic respiratory diseases in later life. For example, these infections increase immune responses, which drive subsequent asthma pathogenesis. Targeting the pathways involved with specific inhibitors or agonists may prevent these consequences of early-life infection. Vaccination and immunomodulatory therapies that control the infections and their sequelae may also be efficacious.

MeSH terms

  • Asthma / etiology
  • Asthma / immunology*
  • Bacterial Infections / drug therapy
  • Bacterial Infections / immunology*
  • Bacterial Infections / prevention & control
  • Chlamydia Infections / drug therapy
  • Chlamydia Infections / immunology
  • Chlamydia trachomatis
  • Chlamydophila pneumoniae
  • Haemophilus Infections / drug therapy
  • Haemophilus Infections / immunology
  • Haemophilus influenzae
  • Humans
  • Immunologic Factors / therapeutic use
  • Interleukin-13 / antagonists & inhibitors
  • Lung / immunology*
  • Pulmonary Disease, Chronic Obstructive / etiology
  • Pulmonary Disease, Chronic Obstructive / immunology*
  • Respiratory Tract Infections / drug therapy
  • Respiratory Tract Infections / immunology*
  • Respiratory Tract Infections / prevention & control
  • Streptococcal Infections / drug therapy
  • Streptococcal Infections / immunology
  • Streptococcal Infections / prevention & control
  • Streptococcal Vaccines / therapeutic use
  • Streptococcus pneumoniae
  • Toll-Like Receptor 2 / agonists

Substances

  • Immunologic Factors
  • Interleukin-13
  • Streptococcal Vaccines
  • Toll-Like Receptor 2