Nasreen Khalil - Academia.edu (original) (raw)
Papers by Nasreen Khalil
The European respiratory journal, 2018
The European respiratory journal, May 1, 2017
Experimental Lung Research, 2002
Canadian Respiratory Journal, 2012
Annals of the American Thoracic Society, 2019
Experimental Lung Research, 2002
In a rat model of lung injury induced bythe antineoplastic antibiotic, bleomycin, there is loss o... more In a rat model of lung injury induced bythe antineoplastic antibiotic, bleomycin, there is loss of type I alveolar epithelial cells (AECs) followed by infiltration of activated inflammatory cells, type II AEC proliferation, and fibrosis. At 4 and 7 days after bleomycin administration alveolar macrophages have increased production and release of active transforming growth factor (TGF)- β 1, an inhibitor of epithelial cell proliferation. Paradoxically at these same time intervals there is a concomitant induction of type II AEC proliferation. For TGF- β -mediated signal transduction to occur, the expression of both TGF- β receptor types I (T β R-I) and II (T β R-II) must be present. Using immunohistochemistry and in situ hybridization, 4 and 7 days after bleomycin administration the expression of T β R-I on AECs was reduced whereas that of T β R-II was unaltered. However, 14 and 28 days after bleomycin injury, when there is decreased proliferation and induction of differentiation of type II AECs, there was a return of T β R-I expression on AECs. In contrast, T β R-I and T β R-II were observed on interstitial fibroblasts at all time intervals after bleomycin administration. Because both T β R-I and T β R-II are required for signal transduction, the reduction of T β R-I levels on the alveolar epithelium may alter the sensitivity of AECs to the antiproliferative effects of TGF- β 1 present in increased quantities following bleomycin injury. The loss of an antiproliferative response to TGF- β 1 may be important for the regeneration of the alveolar epithelium by proliferation while the expression of both receptors on fibroblasts would result in TGF- β 1 signaling for the synthesis of connective tissue proteins. Our findings suggest that during bleomycin-induced pulmonary fibrosis, the effects of TGF- β 1 on cells may be regulated by the expression of T β Rs.
Annals of the American Thoracic Society, Apr 1, 2019
American Journal of Physiology-lung Cellular and Molecular Physiology, Mar 1, 2003
Toxicologic Pathology, 2007
Annals of the Rheumatic Diseases
BackgroundLung imaging findings vary among subtypes of connective tissue disease-associated inter... more BackgroundLung imaging findings vary among subtypes of connective tissue disease-associated interstitial lung disease (CTD-ILD), leading to both diagnostic and therapeutic challenges.ObjectivesWe performed a comprehensive assessment of ILD morphology across CTD-ILD subtypes by examining the presence of overall imaging patterns and specific morphological features.MethodsHigh-resolution chest computed tomography (HRCT) of patients with CTD-ILD enrolled in the multicentre Canadian Registry for Pulmonary Fibrosis from their first ILD clinic visit were re-reviewed in standardized multidisciplinary discussion. All CTD diagnoses were rheumatologist-confirmed. An experienced chest radiologist blinded to clinical data quantified the percentage of lung parenchyma affected by honeycombing, reticulation, ground glass opacity (GGO), hypoattenuating lobules, consolidation, and emphysema. Gas trapping was evaluated on expiratory CT. Each case was categorized into an overall disease pattern includi...
Annals of the Rheumatic Diseases
BackgroundPrognosis in connective tissue disease associated interstitial lung disease (CTD-ILD) i... more BackgroundPrognosis in connective tissue disease associated interstitial lung disease (CTD-ILD) is influenced by the underlying diagnosis and chest imaging pattern. Usual interstitial pneumonia (UIP), non-specific interstitial pneumonia (NSIP), and fibrotic hypersensitivity pneumonitis (fHP) patterns can be found across all CTD-ILD subtypes although their impact on disease evolution and treatment response is unclear.ObjectivesOur goal was to examine the association of lung imaging pattern with CTD-ILD progression, mortality, and immunosuppression response.Methods615 patients with CTD-ILD enrolled in the Canadian Registry for Pulmonary Fibrosis had high-resolution chest computed tomography (HRCT) from their first ILD clinic visit reviewed in standardized multidisciplinary discussion. All CTD diagnoses were rheumatologist-confirmed. Experienced chest radiologists blinded to clinical data categorized each case into five groups: UIP, NSIP, organizing pneumonia (OP), fHP, and other patte...
D22. ADDRESSING HEALTH DISPARITIES IN LUNG DISEASE
Respiratory Research, Jan 3, 2006
The European respiratory journal, 2018
The European respiratory journal, May 1, 2017
Experimental Lung Research, 2002
Canadian Respiratory Journal, 2012
Annals of the American Thoracic Society, 2019
Experimental Lung Research, 2002
In a rat model of lung injury induced bythe antineoplastic antibiotic, bleomycin, there is loss o... more In a rat model of lung injury induced bythe antineoplastic antibiotic, bleomycin, there is loss of type I alveolar epithelial cells (AECs) followed by infiltration of activated inflammatory cells, type II AEC proliferation, and fibrosis. At 4 and 7 days after bleomycin administration alveolar macrophages have increased production and release of active transforming growth factor (TGF)- β 1, an inhibitor of epithelial cell proliferation. Paradoxically at these same time intervals there is a concomitant induction of type II AEC proliferation. For TGF- β -mediated signal transduction to occur, the expression of both TGF- β receptor types I (T β R-I) and II (T β R-II) must be present. Using immunohistochemistry and in situ hybridization, 4 and 7 days after bleomycin administration the expression of T β R-I on AECs was reduced whereas that of T β R-II was unaltered. However, 14 and 28 days after bleomycin injury, when there is decreased proliferation and induction of differentiation of type II AECs, there was a return of T β R-I expression on AECs. In contrast, T β R-I and T β R-II were observed on interstitial fibroblasts at all time intervals after bleomycin administration. Because both T β R-I and T β R-II are required for signal transduction, the reduction of T β R-I levels on the alveolar epithelium may alter the sensitivity of AECs to the antiproliferative effects of TGF- β 1 present in increased quantities following bleomycin injury. The loss of an antiproliferative response to TGF- β 1 may be important for the regeneration of the alveolar epithelium by proliferation while the expression of both receptors on fibroblasts would result in TGF- β 1 signaling for the synthesis of connective tissue proteins. Our findings suggest that during bleomycin-induced pulmonary fibrosis, the effects of TGF- β 1 on cells may be regulated by the expression of T β Rs.
Annals of the American Thoracic Society, Apr 1, 2019
American Journal of Physiology-lung Cellular and Molecular Physiology, Mar 1, 2003
Toxicologic Pathology, 2007
Annals of the Rheumatic Diseases
BackgroundLung imaging findings vary among subtypes of connective tissue disease-associated inter... more BackgroundLung imaging findings vary among subtypes of connective tissue disease-associated interstitial lung disease (CTD-ILD), leading to both diagnostic and therapeutic challenges.ObjectivesWe performed a comprehensive assessment of ILD morphology across CTD-ILD subtypes by examining the presence of overall imaging patterns and specific morphological features.MethodsHigh-resolution chest computed tomography (HRCT) of patients with CTD-ILD enrolled in the multicentre Canadian Registry for Pulmonary Fibrosis from their first ILD clinic visit were re-reviewed in standardized multidisciplinary discussion. All CTD diagnoses were rheumatologist-confirmed. An experienced chest radiologist blinded to clinical data quantified the percentage of lung parenchyma affected by honeycombing, reticulation, ground glass opacity (GGO), hypoattenuating lobules, consolidation, and emphysema. Gas trapping was evaluated on expiratory CT. Each case was categorized into an overall disease pattern includi...
Annals of the Rheumatic Diseases
BackgroundPrognosis in connective tissue disease associated interstitial lung disease (CTD-ILD) i... more BackgroundPrognosis in connective tissue disease associated interstitial lung disease (CTD-ILD) is influenced by the underlying diagnosis and chest imaging pattern. Usual interstitial pneumonia (UIP), non-specific interstitial pneumonia (NSIP), and fibrotic hypersensitivity pneumonitis (fHP) patterns can be found across all CTD-ILD subtypes although their impact on disease evolution and treatment response is unclear.ObjectivesOur goal was to examine the association of lung imaging pattern with CTD-ILD progression, mortality, and immunosuppression response.Methods615 patients with CTD-ILD enrolled in the Canadian Registry for Pulmonary Fibrosis had high-resolution chest computed tomography (HRCT) from their first ILD clinic visit reviewed in standardized multidisciplinary discussion. All CTD diagnoses were rheumatologist-confirmed. Experienced chest radiologists blinded to clinical data categorized each case into five groups: UIP, NSIP, organizing pneumonia (OP), fHP, and other patte...
D22. ADDRESSING HEALTH DISPARITIES IN LUNG DISEASE
Respiratory Research, Jan 3, 2006