Inflammatory and immune dysregulation associated lung disease
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Principal Investigator: Kenneth Olivier Organization: NATIONAL HEART, LUNG, AND BLOOD INSTITUTE Fiscal Year: 2020 Award: $289,215 Funding agency: National Heart Lung and Blood Institute The pulmonary involvement in disorders of immune or inflammatory regulation can range from a primary manifestation such as with sarcoidosis or a relatively minor manifestations such as seen with the Mendelian Susceptibility to Mycobacterial Disease immune deficiencies. While both of these can be associated with granulomatous inflammation in the lung, the clinical pulmonary manifestations are quite different as are the management strategies. The Laboratory of Chronic Airway Infection (LCAI) has sought to capitalize on the close collaboration with the Laboratory of Clinical Immunology and Microbiology and other branches within the NIAID and NIAMS focused on these disorders to describe the pulmonary manifestations of known and emerging immune and inflammatory diseases. Over the past year we have continued collaboration with investigators at the University of North Carolina to better define the role of STAT3 in altered airway clearance. Airway cells collected as part of this collaboration were utilized by UNC collaborators to characterize the airway epithelial interaction with the novel SARS CoV-2 virus to provide a plausible explanation for its transit from the upper to lower respiratory tract. Bone marrow derived mesenchymal stromal cells were shown to modulate in vitro the inflammation associated with sarcoidosis associated macrophage, setting the stage for a potential therapeutic intervention in this disease. Pulmonary function was characterised in 2 rare conditions, Multiple Endocrine Neoplasia 2B and dyskeratosis congenita. Finally, a new disorder of immune regulation, PI3Kgamma deficiency was described in a patient with recurring lymphocyte-predominant lung infiltrates and insights into the inflammatory pathway were gleaned from a novel mouse model. Terms: <2019 novel coronavirus><2019-nCoV><Autoimmune Diseases><Autoimmune Polyendocrinopathies><Besnier-Boeck Disease><Boeck's Sarcoid><Bone Marrow><Bone Marrow Reticuloendothelial System><Candidiasis><Candidosis><Cell Body><Cells><Chronic><Chronic Granulomatous Disease><Clinical><Clinical Immunology><Clinical Microbiology><Cole syndrome><Cole-Rauschkolb-Toomey syndrome><Collaborations><Congenital Ectodermal Defect><Deficiency Diseases><Disease><Disorder><Dysfunction><Dyskeratosis Congenita><Ectodermal Dysplasia><Endocrine><Engman syndrome><Functional disorder><Genetic><Genetic Alteration><Genetic Change><Genetic defect><Glean><Goals><Granulomatous><Host Defense><Hyper-IgE Syndrome><Hyperimmunoglobulin E Syndrome><Hyperimmunoglobulin E-Recurrent Infection Syndrome><IgE><Immune><Immune Diseases><Immune Disorders><Immune Dysfunction><Immune System Diseases><Immune System Disorder><Immune System Dysfunction><Immune System and Related Disorders><Immunes><Immunodeficiency and Immunosuppression Disorders><Immunoglobulin E><Immunologic Diseases><Immunological Diseases><Immunological Dysfunction><Immunological System Dysfunction><Immunomodulation><In Vitro><Infection><Inflammation><Inflammatory><Investigators><Job's Syndrome><Laboratories><Link><Lower respiratory tract structure><Lung><Lung Respiratory System><Lung diseases><Lung infections><Lymphocyte><Lymphocytic><Minor><Moniliasis><Mutation><NIAID><NIAMS><National Institute of Allergy and Infectious Disease><National Institute of Arthritis and Musculoskeletal and Skin Diseases><Neoplasms><North Carolina><PI3CG><PI3KGamma><PI3k><PIK3><PIK3CG><PIK3CG gene><Pathway interactions><Patients><Physiopathology><Predisposition><Pulmonary Diseases><Pulmonary Disorder><Regulation><Research Personnel><Researchers><Respiratory Disease><Respiratory System Disease><Respiratory System Disorder><Role><SARS-CoV-2><SARS-CoV2><SARS-associated coronavirus 2><SARS-coronavirus-2><SARS-related coronavirus 2><STAT3><STAT3 gene><Sarcoidosis><Schaumann's Disease><Severe acute respiratory syndrome coronavirus 2><Susceptibility><Syndrome><Therapeutic Intervention><Universities><Virus><Wuhan coronavirus><X-Linked Dyskeratosis Congenita><Zinsser syndrome><Zinsser-Engman-Cole syndrome><airway epithelium><autoimmune disorder><congenital dyskeratosis><disease of the lung><disorder of the lung><genome mutation><immune modulation><immune regulation><immune regulator><immunologic reactivity control><immunomodulatory><immunoregulation><immunoregulatory><improved><insight><intervention therapy><lower respiratory tract><lung disorder><lymph cell><macrophage><mesenchymal stromal cell><mouse model><murine model><mycobacterial><neoplasia><neoplastic growth><novel><pathophysiology><pathway><pulmonary><pulmonary function><pulmonary infections><rare condition><rare syndrome><social role>