Lymphocytes in cystic fibrosis lung disease: a tale of two immunities (Q47981706)

7 February 2018

title

Lymphocytes in cystic fibrosis lung disease: a tale of two immunities (English)

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7 February 2018

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R B Moss

1

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7 February 2018

publication date

1 March 2004

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7 February 2018

Clinical and Experimental Immunology

published in

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7 February 2018

volume

135

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7 February 2018

issue

3

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7 February 2018

page(s)

358-360

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7 February 2018

Update on pathogenesis of cystic fibrosis lung disease

cites work

1 reference

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State of the Art: Why do the lungs of patients with cystic fibrosis become infected and why can't they clear the infection?

21 January 2018

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Transcriptional adaptation to cystic fibrosis transmembrane conductance regulator deficiency

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Modifier genes in cystic fibrosis lung disease.

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Plasma membrane CFTR regulates RANTES expression via its C-terminal PDZ-interacting motif

21 January 2018

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Lung inflammation early in cystic fibrosis: bugs are indicted, but the defense is guilty.

21 January 2018

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Inflammatory response in airway epithelial cells isolated from patients with cystic fibrosis.

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The immunoevasive activities of Pseudomonas aeruginosa. Relevance for cystic fibrosis

21 January 2018

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Cystic fibrosis airway epithelia fail to kill bacteria because of abnormal airway surface fluid.

21 January 2018

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Activity of abundant antimicrobials of the human airway

21 January 2018

1 reference

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Salt-independent abnormality of antimicrobial activity in cystic fibrosis airway surface fluid

21 January 2018

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Statin-mediated correction of STAT1 signaling and inducible nitric oxide synthase expression in cystic fibrosis epithelial cells

21 January 2018

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Reduced IL-10 secretion by CD4+ T lymphocytes expressing mutant cystic fibrosis transmembrane conductance regulator (CFTR).

21 January 2018

1 reference

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Peripheral decrease and pulmonary homing of CD4+CD45RO+ helper memory T cells in cystic fibrosis.

21 January 2018

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Inflammation and infection in naive human cystic fibrosis airway grafts

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Primary inflammation in human cystic fibrosis small airways

21 January 2018

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G551D Cystic Fibrosis Mice Exhibit Abnormal Regulation of Inflammation in Lungs and Macrophages

21 January 2018

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CCL20 is an inducible product of human airway epithelia with innate immune properties.

21 January 2018

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Dysregulation of IL-2 and IL-8 production in circulating T lymphocytes from young cystic fibrosis patients

21 January 2018

1 reference

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Impaired Innate Host Defense Causes Susceptibility to Respiratory Virus Infections in Cystic Fibrosis

2 November 2018

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Mucus clearance as a primary innate defense mechanism for mammalian airways

2 November 2018

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Distinct fates of monocytes and T cells directly activated by Pseudomonas aeruginosa exoenzyme S.

2 November 2018

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Proinflammatory cytokine responses to P. aeruginosa infection in human airway epithelial cell lines

2 November 2018

1 reference

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The innate immune system in cystic fibrosis lung disease

2 November 2018

1 reference

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Early alterations in airway mucociliary clearance and inflammation of the lamina propria in CF mice

2 November 2018

1 reference

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Nonopsonic antibodies in cystic fibrosis. Pseudomonas aeruginosa lipopolysaccharide-specific immunoglobulin G antibodies from infected patient sera inhibit neutrophil oxidative responses

2 November 2018

1 reference

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Neutrophil elastase cleaves C3bi on opsonized pseudomonas as well as CR1 on neutrophils to create a functionally important opsonin receptor mismatch

2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1808975

Human lymphocytes transcribe the cystic fibrosis transmembrane conductance regulator gene and exhibit CF-defective cAMP-regulated chloride current

2 November 2018

1 reference

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Cellular immunity to bacteria: impairment of in vitro lymphocyte responses to Pseudomonas aeruginosa in cystic fibrosis patients

2 November 2018

1 reference

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Cytokine dysregulation in activated cystic fibrosis (CF) peripheral lymphocytes

2 November 2018

1 reference

12 December 2020

The immune response to chronic Pseudomonas aeruginosa lung infection in cystic fibrosis patients is predominantly of the Th2 typeNote

1 reference

12 December 2020

Quantitative analysis of inflammatory cells infiltrating the cystic fibrosis airway mucosa

1 reference

12 December 2020

Dysregulated NF-kappaB activation in cystic fibrosis: evidence for a primary inflammatory disorder

1 reference

12 December 2020

Distinct pattern of immune cell population in the lung of human fetuses with cystic fibrosis

1 reference

12 December 2020

Functional IL-10 deficiency in the lung of cystic fibrosis (cftr(-/-)) and IL-10 knockout mice causes increased expression and function of B7 costimulatory molecules on alveolar macrophages

1 reference

12 December 2020

Distinct cytokine production by lung and blood neutrophils from children with cystic fibrosis

1 reference

12 December 2020

Immunoglobulin production in bronchial mucosa and bronchial lymph nodes, particularly in cystic fibrosis of the pancreas

1 reference

12 December 2020

Studies on the mechanism of T cell inhibition by the Pseudomonas aeruginosa phenazine pigment pyocyanine

1 reference

12 December 2020

T lymphocytes and activated eosinophils in airway mucosa in fatal asthma and cystic fibrosis

1 reference

12 December 2020

Expression and regulation of tumor necrosis factor in macrophages from cystic fibrosis patients

1 reference

12 December 2020

Altered respiratory epithelial cell cytokine production in cystic fibrosis

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12 December 2020

High susceptibility for cystic fibrosis human airway gland cells to produce IL-8 through the I kappa B kinase alpha pathway in response to extracellular NaCl content

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12 December 2020

10.1111/J.1365-2249.2003.02389.X

Identifiers

DOI

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7 February 2018

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7 February 2018