Publications by authors named "Dalen C"

Background: Asthma inflammatory phenotypes are often defined by relative cell counts of airway eosinophils/neutrophils. However, the importance of neutrophilia remains unclear, as does the effect of ICS treatment on asthma phenotypes and airway neutrophil function. The purpose of this study was to assess asthma phenotype prevalence/characteristics in a community setting, and, in a nested preliminary study, determine how treatment changes affect phenotype stability and inflammation, with particular focus on airway neutrophils.

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Sputum basophil numbers are increased in allergic asthmatics, but it is unclear what role airway basophils play in "TH2-low" asthma phenotypes. Using flow cytometry, we found that basophils were significantly increased in all asthmatics (n=26) compared with healthy controls (n=8) (P=0.007) with highest levels observed in eosinophilic asthma (EA); median 0.

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Background And Objective: Neutrophilic inflammation has been implicated in non-eosinophilic asthma (NEA) in adults, but little is known about NEA in children/adolescents. We assessed clinical and inflammatory characteristics of NEA in adolescent asthma.

Methods: Airway inflammation, sputum endotoxin, airway hyper-reactivity, atopy and lung function were assessed in 77 adolescents with asthma and 68 without asthma (12-17 years).

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Background And Objective: Increased sputum neutrophilia has been observed in asthma, but also during normal ageing in asthmatics and non-asthmatics. It remains unclear what constitutes 'normal' neutrophil levels in different age groups.

Methods: We assessed the relationship between age and airway neutrophils of 194 asthmatics and 243 non-asthmatics (age range: 6-80 years).

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Background: Airway inflammation is commonly assessed by sputum induction followed by a differential cell count (DCC) using light microscopy. This method is prone to intercounter variability and poor reproducibility. We aimed to develop a more objective method using flow cytometry (FCM).

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There has been a global epidemic of asthma during the past half-century. More recently, the prevalence has leveled off or declined in many Western countries, whereas the prevalence in less affluent nations is still increasing. The reasons for this and the different geographical patterns of asthma prevalence remain unclear.

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Background And Objective: Measuring the fraction of nitric oxide in exhaled breath (FE(NO)) is increasingly utilized to assess airway inflammation in asthma. The primary aim of this study was to compare exhaled nitric oxide measurements obtained using two devices from different manufacturers, that is, the recently marketed portable and electrochemical-based Medisoft HypAir FE(NO) and the well-established chemiluminescence-based Aerocrine NIOX analyzer, in an unselected population.

Methods: FE(NO) measurements were conducted in 106 subjects (86 healthy; 20 asthmatic; 56.

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Background: Inhaled corticosteroids are widely used in the treatment of persistent asthma, usually combined with inhaled beta2-agonists. Previous research suggests that short-acting beta2-agonists (SABAs) may downregulate the anti-inflammatory effects of inhaled corticosteroids, thereby increasing asthma morbidity.

Objective: To determine whether 3-bromotyrosine and 3,5-dibromotyrosine levels, specific markers of eosinophil activation, reflect treatment effects on airway inflammation of inhaled corticosteroids and SABAs and support previous conclusions.

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Objective: To determine whether lung function alters asthma severity based on symptom history in asthmatic adolescents.

Design: Data on asthma symptoms and lung function were collected from adolescents randomly selected from the general population.

Setting: Five schools from the central Wellington, New Zealand, area during 2003 to 2005.

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Asthma control, defined by asthma symptoms and lung function, and asthma medication use, was assessed in 123 adolescent asthmatics. Sputum eosinophilia (>or= 2.5% eosinophils) and bronchial hyperresponsiveness (BHR) to hypertonic saline were also measured to assess whether these additional objective parameters might aid in determining asthma control; 54.

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Eosinophil peroxidase is a haem enzyme of eosinophils that is implicated in oxidative tissue injury in asthma. It uses hydrogen peroxide to oxidize thiocyanate and bromide to their respective hypohalous acids. Nitrite is also a substrate for eosinophil peroxidase.

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Eosinophil peroxidase and myeloperoxidase use hydrogen peroxide to produce hypobromous acid and hypochlorous acid. These powerful oxidants may damage the lungs if they are produced as part of the inflammatory response in asthma. The aim of this study was to determine if peroxidases generate hypohalous acids in the airways of individuals with stable asthma, and if they affect lung function.

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Article Synopsis
  • Eosinophil peroxidase plays a role in tissue damage during inflammatory conditions by using hydrogen peroxide (H2O2) to oxidize halides into hypohalous acids.
  • Researchers measured H2O2 usage by the enzyme, determining that thiocyanate is preferred over bromide for oxidation, with catalytic constants of 248 s(-1) for bromide and 223 s(-1) for thiocyanate.
  • The study suggests that eosinophil peroxidase can produce hypobromous acid and thiocyanate oxidation products under physiological conditions, and that thiocyanate may enhance peroxidase-induced toxicity due to its conversion of hypothiocyanite into a more potent oxidant.
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Myeloperoxidase is a heme enzyme of neutrophils that uses hydrogen peroxide to oxidize chloride to hypochlorous acid. Recently, it has been shown to catalyze nitration of tyrosine. In this study we have investigated the mechanism by which it oxidizes nitrite and promotes nitration of tyrosyl residues.

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Article Synopsis
  • Myeloperoxidase, an enzyme in neutrophils, utilizes hydrogen peroxide (H2O2) to oxidize different substrates like chloride, bromide, iodide, and thiocyanate, with chloride being the primary one studied.
  • Research showed that thiocyanate is a significantly preferred substrate over chloride and bromide, with specific constants indicating a strong preference (1:60:730).
  • The study found that even at high chloride concentrations (100 mM), myeloperoxidase effectively produced hypothiocyanite from thiocyanate, suggesting its vital role in physiological conditions related to inflammation and host defense.
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Article Synopsis
  • The alloantisera Ond and Mart target specific polymorphisms in the alpha L and alpha M subunits of beta 2 integrins (CD11a and CD11b) and were tested using various immunological methods on cells from normal donors and patients with leukocyte adhesion deficiency.
  • Molecular analysis revealed that the Ond(a) antigen is caused by a G2466C DNA substitution in the alpha L subunit, leading to an Arg766Thr amino acid change, while the Mart(a) antigen results from a G302A substitution in the alpha M subunit, causing an Arg61His change.
  • The study confirms the relationship between these point mutations and their associated serologic phenotypes, highlighting the
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The human neutrophil-specific alloantigen NB1 was identified as a glycosyl-phosphatidylinositol (GPI)-anchored N-glycosylated protein of M(r) 56-62 kD under reducing conditions. Under non-reducing conditions its M(r) was 49-55 kD. This glycoprotein antigen was found to be expressed by only a subpopulation of normal donor neutrophils, and could not be detected on other blood cells.

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Objective: To determine the efficacy of antenatal low dose oral betamethasone in preventing neonatal thrombocytopenia and/or bleeding in infants of mothers with idiopathic thrombocytopenic purpura (ITP).

Setting: Hospital department of obstetrics and gynaecology, referral centre.

Patients: 41 pregnancies in 38 women were randomized.

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The antigen recognized by the monoclonal antibody Ki-67 is a proliferation-related nucleolus-associated constituent used as a marker for cycling cells in tumor diagnosis. Antibody Ki-67 reacts with human proliferating cells, but not with hamster and mouse cells. Expression of the Ki-67 antigen was studied in a panel of human-rodent somatic cell hybrids.

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Article Synopsis
  • Autoantibodies against platelets and granulocytes are commonly found in individuals with AIDS or at risk from AIDS, with significant presence in both symptomatic and some asymptomatic populations.
  • In a study, immunofluorescence revealed platelet-bound immunoglobulins in all AIDS patients and a portion of individuals with AIDS-related complex, indicating an immune response related to the disease.
  • The findings suggest that these autoantibodies, rather than just increased immune complexes, play a role in the immune profile of these patients, while showing no correlation with platelet and granulocyte counts.
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The sensitivity and specificity of the platelet immunofluorescence test for the diagnosis of idiopathic thrombocytopenia (ITP) was studied in a series of 255 patients. Patients' platelets were tested directly. Diethyl-ether eluates of these platelets and patients' sera were tested indirectly with normal donor platelets.

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The strong association between HLA-DR3 and Zwa alloimmunization in Zwa-negative mothers, resulting in the production of anti-Zwa antibodies and ultimately in neonatal alloimmune thrombocytopenic purpura (NAITP) in the newborn, could be confirmed. In addition, we have shown an equally strong association between HLA-DR3 and Zwa alloimmunization in Zwa-negative recipients of blood transfusions, resulting in posttransfusion purpura (PTP). However, the strongest association both in mothers of NAITP patients and in PTP patients was observed with the supertypic DRw52 antigen.

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