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Animal models of asthma: Reprise or reboot?
- Source :
- Biochemical Pharmacology. 87:131-139
- Publication Year :
- 2014
- Publisher :
- Elsevier BV, 2014.
-
Abstract
- Animal models of disease represent the pinnacle of hierarchical research efforts to validate targets and compounds for therapeutic intervention. Yet models of asthma, particularly in the mouse, which, for practical reasons, has become the sine qua non of asthma research, have been a bone of contention for decades. With barely a nod to their limitations and an extensive history of translational failures, they continue to be used for target identification and to justify the clinical evaluation of new compounds. Recent improvements - including sensitization directly to the airways; use of more relevant allergens; development of a chronic rather than short-term condition; utilization of techniques to measure lung function beyond uninterpretable measures of airway hyperresponsiveness - are laudable but cannot bridge the chasm between the models and the myriad complexities of the human disorder and multiple asthma endophenotypes. While further model developments are necessary, including recognition of key environmental factors beyond allergens, the judicious integration with newer ex vivo and in vitro techniques, including human precision-cut lung slices, reprograming of patient-derived induced pluripotent stem cells and fibroblasts to epithelial and smooth muscle cells, and use of other clinical samples to create a more holistic depiction of activities, might improve their translational success.
- Subjects :
- Pharmacology
In Vitro Techniques
Uninterpretable
Sine qua non
business.industry
Myocytes, Smooth Muscle
Disease
medicine.disease
Biochemistry
Asthma
respiratory tract diseases
Disease Models, Animal
Smooth muscle
Immunology
medicine
Animals
Humans
Anti-Asthmatic Agents
Induced pluripotent stem cell
business
Lung
Neuroscience
Reboot
Subjects
Details
- ISSN :
- 00062952
- Volume :
- 87
- Database :
- OpenAIRE
- Journal :
- Biochemical Pharmacology
- Accession number :
- edsair.doi.dedup.....be99b09ec1567d952bab94cec33b61db
- Full Text :
- https://doi.org/10.1016/j.bcp.2013.06.026