Literature DB >> 28658552

Mechanisms and treatments for severe, steroid-resistant allergic airway disease and asthma.

Philip M Hansbro1, Richard Y Kim1, Malcolm R Starkey1, Chantal Donovan1, Kamal Dua1, Jemma R Mayall1, Gang Liu1, Nicole G Hansbro1, Jodie L Simpson1, Lisa G Wood1, Jeremy A Hirota2, Darryl A Knight1, Paul S Foster1, Jay C Horvat1.   

Abstract

Severe, steroid-resistant asthma is clinically and economically important since affected individuals do not respond to mainstay corticosteroid treatments for asthma. Patients with this disease experience more frequent exacerbations of asthma, are more likely to be hospitalized, and have a poorer quality of life. Effective therapies are urgently required, however, their development has been hampered by a lack of understanding of the pathological processes that underpin disease. A major obstacle to understanding the processes that drive severe, steroid-resistant asthma is that the several endotypes of the disease have been described that are characterized by different inflammatory and immunological phenotypes. This heterogeneity makes pinpointing processes that drive disease difficult in humans. Clinical studies strongly associate specific respiratory infections with severe, steroid-resistant asthma. In this review, we discuss key findings from our studies where we describe the development of representative experimental models to improve our understanding of the links between infection and severe, steroid-resistant forms of this disease. We also discuss their use in elucidating the mechanisms, and their potential for developing effective therapeutic strategies, for severe, steroid-resistant asthma. Finally, we highlight how the immune mechanisms and therapeutic targets we have identified may be applicable to obesity-or pollution-associated asthma.
© 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  infection; novel therapies; obesity; pollution; severe asthma; steroid resistance

Mesh:

Substances:

Year:  2017        PMID: 28658552     DOI: 10.1111/imr.12543

Source DB:  PubMed          Journal:  Immunol Rev        ISSN: 0105-2896            Impact factor:   12.988


  30 in total

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Review 3.  IL-33 in Chronic Respiratory Disease: From Preclinical to Clinical Studies.

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4.  [Inhibition of TAK1 aggravates airway inflammation by increasing RIPK1 activity and promoting macrophage death in a mouse model of toluene diisocyanate-induced asthma].

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6.  Targeting the phosphorylation site of myristoylated alanine-rich C kinase substrate alleviates symptoms in a murine model of steroid-resistant asthma.

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Review 7.  Emerging concepts and directed therapeutics for the management of asthma: regulating the regulators.

Authors:  Madhur D Shastri; Wai Chin Chong; Kamal Dua; Gregory M Peterson; Rahul P Patel; Malik Q Mahmood; Murtaza Tambuwala; Dinesh K Chellappan; Nicole G Hansbro; Shakti D Shukla; Philip M Hansbro
Journal:  Inflammopharmacology       Date:  2020-11-05       Impact factor: 4.473

8.  TH17 cells and corticosteroid insensitivity in severe asthma.

Authors:  Yan Xie; Peter W Abel; Thomas B Casale; Yaping Tu
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9.  Apolipoprotein E is a concentration-dependent pulmonary danger signal that activates the NLRP3 inflammasome and IL-1β secretion by bronchoalveolar fluid macrophages from asthmatic subjects.

Authors:  Elizabeth M Gordon; Xianglan Yao; Haitao Xu; William Karkowsky; Maryann Kaler; Or Kalchiem-Dekel; Amisha V Barochia; Meixia Gao; Karen J Keeran; Kenneth R Jeffries; Stewart J Levine
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Review 10.  Pulmonary group 2 innate lymphoid cells: surprises and challenges.

Authors:  Malcolm R Starkey; Andrew Nj McKenzie; Gabrielle T Belz; Philip M Hansbro
Journal:  Mucosal Immunol       Date:  2019-01-21       Impact factor: 7.313

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