Progress Towards a New Asthma Treatment – Drug Discovery & Development


Drug Discovery & Development

Progress Towards a New Asthma Treatment
Drug Discovery & Development
Source: University of Queensland University of Queensland researchers are developing a new asthma treatment that targets the underlying cause of asthma, rather than just the symptoms. Asthma affects one in 10 Australians and is the most common chronic …

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Endotoxin Exposure during Sensitization to Blomia tropicalis Allergens Shifts TH2 Immunity Towards a TH17-Mediated Airway Neutrophilic Inflammation: Role of TLR4 and TLR2.

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Endotoxin Exposure during Sensitization to Blomia tropicalis Allergens Shifts TH2 Immunity Towards a TH17-Mediated Airway Neutrophilic Inflammation: Role of TLR4 and TLR2.

PLoS One. 2013;8(6):e67115

Authors: Barboza R, Câmara NO, Gomes E, Sá-Nunes A, Florsheim E, Mirotti L, Labrada A, Alcântara-Neves NM, Russo M

Abstract
Experimental evidence and epidemiological studies indicate that exposure to endotoxin lipopolysaccharide (eLPS) or other TLR agonists prevent asthma. We have previously shown in the OVA-model of asthma that eLPS administration during alum-based allergen sensitization blocked the development of lung TH2 immune responses via MyD88 pathway and IL-12/IFN-? axis. In the present work we determined the effect of eLPS exposure during sensitization to a natural airborne allergen extract derived from the house dust mite Blomia tropicalis (Bt). Mice were subcutaneously sensitized with Bt allergens co-adsorbed onto alum with or without eLPS and challenged twice intranasally with Bt. Cellular and molecular parameters of allergic lung inflammation were evaluated 24 h after the last Bt challenge. Exposure to eLPS but not to ultrapure LPS (upLPS) preparation during sensitization to Bt allergens decreased the influx of eosinophils and increased the influx of neutrophils to the airways. Inhibition of airway eosinophilia was not observed in IFN-?deficient mice while airway neutrophilia was not observed in IL-17RA-deficient mice as well in mice lacking MyD88, CD14, TLR4 and, surprisingly, TLR2 molecules. Notably, exposure to a synthetic TLR2 agonist (PamCSK4) also induced airway neutrophilia that was dependent on TLR2 and TLR4 molecules. In the OVA model, exposure to eLPS or PamCSK4 suppressed OVA-induced airway inflammation. Our results suggest that B. tropicalis allergens engage TLR4 that potentiates TLR2 signaling. This dual TLR activation during sensitization results in airway neutrophilic inflammation associated with increased frequency of lung TH17 cells. Our work highlight the complex interplay between bacterial products, house dust mite allergens and TLR signaling in the induction of different phenotypes of airway inflammation.

PMID: 23805294 [PubMed – as supplied by publisher]

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Asthma Patients Tend Towards Depression And Stay Sedentary – Medical News Today


NorthJersey.com

Asthma Patients Tend Towards Depression And Stay Sedentary
Medical News Today
Symptoms of Depression along with unhealthy habits are common amongst individuals with asthma, a telephone survey conducted in Israel found. Aviva Goral, MSc, of the Unit of Mental Health Epidemiology and Psychosocial Aspects of Illness in Tel Hashomer
Asthma Patients Feel Gloomy, Stay SedentaryMedPage Today
Diagnosing asthma in young childrenNorthJersey.com
Depressive symptoms may make asthma control more difficultMedical Xpress
Health Behavior News Service
all 9 news articles »

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Attitudes of clinicians at the Canadian Memorial Chiropractic College towards the chiropractic management of non-musculoskeletal conditions.

Attitudes of clinicians at the Canadian Memorial Chiropractic College towards the chiropractic management of non-musculoskeletal conditions.

J Can Chiropr Assoc. 2011 Jun;55(2):107-19

Authors: Parkinson J, Lau J, Kalirah S, Gleberzon BJ

The objective of this study was to determine the attitudes of clinical faculty during the 2009-2010 academic year at the Canadian Memorial Chiropractic College towards the treatment of various non-musculoskeletal disorders.

PMID: 21629463 [PubMed – in process]

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