TY - JOUR
T1 - Pulmonary disorders, including vocal cord dysfunction
AU - Greenberger, Paul A.
AU - Grammer, Leslie C.
N1 - Funding Information:
Supported by the Ernest S. Bazley Grant to Northwestern Memorial Hospital and Northwestern University
PY - 2010/2
Y1 - 2010/2
N2 - The lung is a very complex immunologic organ and responds in a variety of ways to inhaled antigens, organic or inorganic materials, infectious or saprophytic agents, fumes, and irritants. There might be airways obstruction, restriction, neither, or both accompanied by inflammatory destruction of the pulmonary interstitium, alveoli, or bronchioles. This review focuses on diseases organized by their predominant immunologic responses, either innate or acquired. Pulmonary innate immune conditions include transfusion-related acute lung injury, World Trade Center cough, and acute respiratory distress syndrome. Adaptive immunity responses involve the systemic and mucosal immune systems, activated lymphocytes, cytokines, and antibodies that produce CD4+ TH1 phenotypes, such as for tuberculosis or acute forms of hypersensitivity pneumonitis, and CD4+ TH2 phenotypes, such as for asthma, Churg-Strauss syndrome, and allergic bronchopulmonary aspergillosis.
AB - The lung is a very complex immunologic organ and responds in a variety of ways to inhaled antigens, organic or inorganic materials, infectious or saprophytic agents, fumes, and irritants. There might be airways obstruction, restriction, neither, or both accompanied by inflammatory destruction of the pulmonary interstitium, alveoli, or bronchioles. This review focuses on diseases organized by their predominant immunologic responses, either innate or acquired. Pulmonary innate immune conditions include transfusion-related acute lung injury, World Trade Center cough, and acute respiratory distress syndrome. Adaptive immunity responses involve the systemic and mucosal immune systems, activated lymphocytes, cytokines, and antibodies that produce CD4+ TH1 phenotypes, such as for tuberculosis or acute forms of hypersensitivity pneumonitis, and CD4+ TH2 phenotypes, such as for asthma, Churg-Strauss syndrome, and allergic bronchopulmonary aspergillosis.
KW - Innate
KW - acquired
KW - aspergillosis
KW - bronchiectasis
KW - bronchopulmonary
KW - eosinophilia
KW - hypersensitivity
KW - immunologic
KW - lymphocyte
KW - tuberculosis
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UR - http://www.scopus.com/inward/citedby.url?scp=76749147757&partnerID=8YFLogxK
U2 - 10.1016/j.jaci.2009.09.020
DO - 10.1016/j.jaci.2009.09.020
M3 - Article
C2 - 20176261
AN - SCOPUS:76749147757
SN - 0091-6749
VL - 125
SP - S248-S254
JO - Journal of Allergy and Clinical Immunology
JF - Journal of Allergy and Clinical Immunology
IS - 2 SUPPL. 2
ER -