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Volume 121, Issue 1, Pages 5-10 (January 2008)


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Targeting TNF-α: A novel therapeutic approach for asthma

Christopher Brightling, PhD, MRCPaCorresponding Author Informationemail address, Mike Berry, MD, MRCPb, Yassine Amrani, PhDa

Received 11 September 2007; received in revised form 15 October 2007; accepted 16 October 2007. published online 26 November 2007.

Approximately 5% to 10% of patients with asthma have severe disease that is refractory or poorly responsive to inhaled corticosteroid therapy. These patients represent an important unmet clinical need because they experience considerable morbidity and mortality and consume a disproportionately large amount of health care resources. TNF-α is a proinflammatory cytokine that has been implicated in many aspects of the airway pathology in asthma. Evidence is emerging to suggest that it might play an important role in severe refractory disease. The development of novel TNF-α antagonists has allowed us to test the role of this cytokine in vivo. Preliminary studies have demonstrated an improvement in asthma quality of life, lung function, and airway hyperresponsiveness and a reduction in exacerbation frequency in patients treated with anti–TNF-α therapy. However, there is marked heterogeneity in response, suggesting that benefit is likely to be reserved to a small subgroup. Importantly, where efficacy is reported, this also needs to be considered in the context of concerns about the safety of anti–TNF-α therapies. Therefore the challenge for clinicians is to evaluate the risk/benefit ratio of these therapies in individual patients with asthma.

This activity is available for CME credit. See page 30A for important information.

a Institute of Lung Health, University of Leicester, Leicester, United Kingdom

b University of Birmingham, Edgbaston, Birmingham, United Kingdom

Corresponding Author InformationReprint requests: Christopher Brightling, PhD, MRCP, Institute of Lung Health, University of Leicester, Leicester, LE3 9QP, United Kingdom.

 (Supported by an unrestricted educational grant from Genentech, Inc. and Novartis Pharmaceuticals Corporation)

 Series editors: Donald Y. M. Leung, MD, PhD, and Dennis K. Ledford, MD

 Supported by Asthma UK, a DOH Clinician Scientist award, and NIH06364.

 Disclosure of potential conflict of interest: C. Brightling has consulting arrangements with Cambridge Antibody Technology, GlaxoSmithKline, AstraZeneca, Pfizer, Roche, and Piramed; owns stock in Leicester AIR; has received grant support from AstraZeneca, Cambridge Antibody Technology, and GlaxoSmithKline; and is on the speakers' bureau for AstraZeneca and GlaxoSmithKline. Y. Amrani has received grant support from Centocor and the National Institutes of Health. M. Berry has declared that he has no conflict of interest.

PII: S0091-6749(07)01999-9

doi:10.1016/j.jaci.2007.10.028


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