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Pelargonium sidoides radix extract EPs 7630 reduces rhinovirus infection through modulation of viral binding proteins on human bronchial epithelial cells
Pelargonium sidoides radix extract EPs 7630 reduces rhinovirus infection through modulation of viral binding proteins on human bronchial epithelial cells
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Pelargonium sidoides radix extract EPs 7630 reduces rhinovirus infection through modulation of viral binding proteins on human bronchial epithelial cells
Pelargonium sidoides radix extract EPs 7630 reduces rhinovirus infection through modulation of viral binding proteins on human bronchial epithelial cells

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Pelargonium sidoides radix extract EPs 7630 reduces rhinovirus infection through modulation of viral binding proteins on human bronchial epithelial cells
Pelargonium sidoides radix extract EPs 7630 reduces rhinovirus infection through modulation of viral binding proteins on human bronchial epithelial cells
Journal Article

Pelargonium sidoides radix extract EPs 7630 reduces rhinovirus infection through modulation of viral binding proteins on human bronchial epithelial cells

2019
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Overview
Bronchial epithelial cells are the first target cell for rhinovirus infection. The course of viral infections in patients with acute bronchitis, asthma and COPD can be improved by oral application of Pelargonium sidoides radix extract; however, the mechanism is not well understood. This study investigated the in vitro effect of Pelargonium sidoides radix extract (EPs 7630) on the expression of virus binding cell membrane and host defence supporting proteins on primary human bronchial epithelial cells (hBEC). Cells were isolated from patients with severe asthma (n = 6), moderate COPD (n = 6) and non-diseased controls (n = 6). Protein expression was determined by Western-blot and immunofluorescence. Rhinovirus infection was determined by immunofluorescence as well as by polymerase chain reaction. Cell survival was determined by manual cell count after live/death immunofluorescence staining. All parameters were determined over a period of 3 days. The results show that EPs 7630 concentration-dependently and significantly increased hBEC survival after rhinovirus infection. This effect was paralleled by decreased expression of the inducible co-stimulator (ICOS), its ligand ICOSL and cell surface calreticulin (C1qR). In contrast, EPs 7630 up-regulated the expression of the host defence supporting proteins β-defensin-1 and SOCS-1, both in rhinovirus infected and un-infected hBEC. The expression of other virus interacting cell membrane proteins such as MyD88, TRL2/4 or ICAM-1 was not altered by EPs 7630. The results indicate that EPs 7630 may reduce rhinovirus infection of human primary BEC by down-regulating cell membrane docking proteins and up-regulating host defence proteins.
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject

Adenoviruses

/ Adult

/ Aged

/ Antigens

/ Antiviral Agents - chemistry

/ Antiviral Agents - pharmacology

/ Asthma

/ Asthma - drug therapy

/ Asthma - metabolism

/ Asthma - pathology

/ Asthma - virology

/ Binding

/ Binding proteins

/ Biology and Life Sciences

/ Bronchi - metabolism

/ Bronchi - physiology

/ Bronchitis

/ Calreticulin

/ Cell death

/ Cell membranes

/ Cell surface

/ Cell Survival

/ Cells, Cultured

/ Chronic obstructive lung disease

/ Chronic obstructive pulmonary disease

/ Cytokines

/ Docking

/ Epithelial cells

/ Epithelial Cells - metabolism

/ Epithelial Cells - pathology

/ Epithelial Cells - virology

/ Female

/ Fluorescent antibody technique

/ Gene expression

/ Growth factors

/ Health aspects

/ Hospitals

/ Humans

/ Immunofluorescence

/ Infection

/ Infections

/ Influenza

/ Intercellular adhesion molecule 1

/ Internal medicine

/ Kinases

/ Male

/ Medicine

/ Medicine and Health Sciences

/ Membrane proteins

/ Middle Aged

/ MyD88 protein

/ Patients

/ Pelargonium - chemistry

/ Pelargonium sidoides

/ Peptides

/ Picornaviridae Infections - drug therapy

/ Picornaviridae Infections - metabolism

/ Picornaviridae Infections - pathology

/ Plant Extracts - chemistry

/ Plant Extracts - pharmacology

/ Polymerase chain reaction

/ Protein binding

/ Proteins

/ Pulmonary Disease, Chronic Obstructive - drug therapy

/ Pulmonary Disease, Chronic Obstructive - metabolism

/ Pulmonary Disease, Chronic Obstructive - pathology

/ Pulmonary Disease, Chronic Obstructive - virology

/ Research and Analysis Methods

/ Rhinovirus

/ Rhinovirus - metabolism

/ Rhinoviruses

/ Stimulators

/ Survival

/ Thoracic surgery

/ Viral infections

/ Viruses