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Dive into the research topics where A. Capetandes is active.

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Featured researches published by A. Capetandes.


Annals of Allergy Asthma & Immunology | 2005

Dermatophagoides extract-treated confluent type II epithelial cells (cA549) and human lung mesenchymal cell growth

A. Capetandes; Nathanael S. Horne; Marianne Frieri

BACKGROUND Chronic severe persistent asthma is associated with damaged epithelial cells with discontinuous tight junctions that contribute to dysregulated fibroblast and endothelial cell (mesenchymal) growth. Dermatophagoides species-derived proteases have been shown to cause damage to epithelial cell tight junctions. OBJECTIVE To determine whether Dermatophagoides species can stimulate confluent A549 (cA549), a cell type with discontinuous tight junctions that approximate differentiated type II cells, to undergo altered growth and secrete putative soluble factors that affect the growth of human lung fibroblasts and microvascular endothelial cells. METHODS Dialyzed Dermatophagoides pteronyssinus or Dermatophagoides farinae extracts (0, 300, 600, and 1000 AU/mL) were cultured with and without cA549 in serum-free media for 24 hours. After changes in cA549 growth were recorded, conditioned media from extracts with cA549 (CM) and without cA549 (control media [CTLM]) were transferred to fibroblasts and endothelial cells for 24 hours. Fibroblast and endothelial cell growth responses to CM and CTLM were observed and measured. RESULTS All conditions showed greater than 95% cell viability. Confluent A549 showed dose-dependent growth changes characterized by increased aggregation when incubated with 300, 600, and 1000 AU/mL of D pteronyssinus in serum-free media relative to control. The CM, but not the CTLM, induced dose-dependent aggregation by fibroblasts and endothelial cells. Fibroblasts also showed decreased adhesion when incubated with CM. Dermatophagoides farinae-treated cA549 showed similar but weaker results. The use of serum, boiled CM, or boiled extract inhibited these findings. CONCLUSIONS Dialyzed Dermatophagoides species extracts altered cA549 growth and stimulated the secretion of factors that dysregulate mesenchymal cell growth in vitro.


Allergy and Asthma Proceedings | 2008

The effect of enantiomers of beta-agonists on myofibroblast-derived vascular endothelial growth factor and other matrix components in the presence of dust-mite extract.

Marianne Frieri; A. Capetandes

Beta(2)-adrenergic receptor agonists have been shown to modulate airway epithelial cell and smooth muscle release of cytokines and growth factors transforming growth factor (TGF) beta, associated with remodeling, is known to up-regulate the synthesis of vascular endothelial growth factor (VEGF) and stimulate differentiation of fibroblasts to the myofibroblast phenotype. VEGF and fibronectin can promote angiogenesis and (S)-albuterol can induce VEGF secretion from normal human lung fibroblasts (NHLF). We hypothesize that (S)-albuterol could stimulate myofibroblast secretion and expression of VEGF and fibronectin in the presence of Dermatophagoides pteronyssinus extract. Cultured NHLFs were stimulated with IL-1beta, TGF-beta, D. pteronyssinus, and treated with (R)- and (S)-enantiomers of albuterol. VEGF and fibronectin and basic fibroblast growth factor (bFGF) were measured by ELISA and mRNA. VEGF secretion by fibroblasts was twofold higher with 10(-7) M of (R) relative to (S) (p < 0.05). Myofibroblast secretion of VEGF was increased twofold over fibroblasts, but there was no difference between enantiomers. (S)-albuterol at 10(-8)-10(-4) M caused an increase in VEGF mRNA that paralleled VEGF secretion relative to 10(-8)-10(-4) M. Fibronection secretion by myofibroblasts but not fibroblasts was increased by 10(-5) M of (S) relative to (R) in the presence of recombinant interleukin 1 (rhIL-1)beta and D. pteronyssinus (S)-albuterol at 10(-6) M increased bFGF. The 10(-6) M of (S)-albuterol, but not (R)-albuterol, may promote angiogenesis. Increased fibronectin or bFGF by (S)-albuterol could enhance matrix deposition and remodeling in a subset of asthmatic patients.


Allergy and Asthma Proceedings | 2007

Vascular endothelial growth factor is increased by human pulmonary cells stimulated with Dermatophagoides sp. extract.

A. Capetandes; Minsheng Zhuang; Farah Haque; Linjun Xie; Marianne Frieri


The Journal of Allergy and Clinical Immunology | 2009

Monitoring CD40Ligand in Patients with Systemic Lupus Erythematosus (SLE)

R. Seghal; A. Jabaar; P. Anand; A. Capetandes; Marianne Frieri


The Journal of Allergy and Clinical Immunology | 2004

Dust mite (DM) allergen and IL-1b-stimulated human alveolar epithelial cells (A549) secrete vascular endothelial growth factor (VEGF)

A. Capetandes; L. Xie; Y. Huang; Marianne Frieri


The Journal of Allergy and Clinical Immunology | 2009

Vascular Endothelial Cell Growth Factor (VEGF) Production by Staphylococcal Enterotoxin B (SEB) and IL-1β-Stimulated Human Keratinocytes is Inhibited by Pimecrolimus

Marianne Frieri; A. Capetandes


The Journal of Allergy and Clinical Immunology | 2007

Human Keratinocytes Secrete TNFa Stimulated With Cytomix and D. Pteronyssinus Extract

Marianne Frieri; A. Capetandes


The Journal of Allergy and Clinical Immunology | 2006

(R)-, But Not (S)-, Enantiomers of Beta2 Agonists Inhibit IL-8Secretion by RSV Antigen-Stimulated Confluent HumanAlveolar Epithelial Cells (cA549)

Marianne Frieri; A. Capetandes


The Journal of Allergy and Clinical Immunology | 2006

MMP-9/TIMP-1 Ratio in Confluent Human Alveoloar Epithelial Cells (cA549) Stimulated by D. Pteronyssinus

J. Zimmermann; A. Capetandes; Marianne Frieri


The Journal of Allergy and Clinical Immunology | 2006

10-6M (RR)-Formoterol, but Not (SS)-Formoterol or (S)/(R)-Albuterol, Inhibits RANTES Secretion by RSV Antigen-Stimulated Confluent Human Alveolar Epithelial Cells (cA549)

G. Puglisi; A. Capetandes; Marianne Frieri

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Marianne Frieri

Nassau University Medical Center

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J. Zimmermann

Nassau University Medical Center

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A. Jabaar

Nassau University Medical Center

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G. Puglisi

Nassau University Medical Center

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L. Xie

Nassau University Medical Center

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Nathanael S. Horne

Nassau University Medical Center

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P. Anand

Nassau University Medical Center

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R. Seghal

Nassau University Medical Center

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Y. Huang

Nassau University Medical Center

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Farah Haque

Tata Institute of Fundamental Research

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