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Inflammatory mechanisms linking maternal and childhood asthma
Author(s) -
Lebold Katie M.,
Jacoby David B.,
Drake Matthew G.
Publication year - 2020
Publication title -
journal of leukocyte biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.819
H-Index - 191
eISSN - 1938-3673
pISSN - 0741-5400
DOI - 10.1002/jlb.3mr1219-338r
Subject(s) - asthma , immunology , medicine , offspring , inflammation , immune system , allergy , fetus , pregnancy , biology , genetics
Asthma is a chronic inflammatory airway disease characterized by airway hyperresponsiveness, inflammation, and remodeling. Asthma often develops during childhood and causes lifelong decrements in lung function and quality of life. Risk factors for childhood asthma are numerous and include genetic, epigenetic, developmental, and environmental factors. Uncontrolled maternal asthma during pregnancy exposes the developing fetus to inflammatory insults, which further increase the risk of childhood asthma independent of genetic predisposition. This review focuses on the role of maternal asthma in the development of asthma in offspring. We will present maternal asthma as a targetable and modifiable risk factor for childhood asthma and discuss the mechanisms by which maternal inflammation increases childhood asthma risk. Topics include how exposure to maternal asthma in utero shapes structural lung development with a special emphasis on airway nerves, how maternal type‐2 cytokines such as IL‐5 activate the fetal immune system, and how changes in lung and immune cell development inform responses to aero‐allergens later in life. Finally, we highlight emerging evidence that maternal asthma establishes a unique “asthma signature” in the airways of children, leading to novel mechanisms of airway hyperreactivity and inflammatory cell responses.