The Journal of Allergy and Clinical Immunology
Volume 121, Issue 1 , Pages 5-10, January 2008

Targeting TNF-α: A novel therapeutic approach for asthma

  • Christopher Brightling, PhD, MRCP

      Affiliations

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

      Affiliations

    • University of Birmingham, Edgbaston, Birmingham, United Kingdom
  • ,
  • Yassine Amrani, PhD

      Affiliations

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

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

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

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.

Key words: Asthma, refractory asthma, TNF-α, mast cells, airway smooth muscle

Abbreviations used: AHR, Airway hyperresponsiveness, ASM, Airway smooth muscle, mTNF-α, Membrane TNF-α

 

 (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

The Journal of Allergy and Clinical Immunology
Volume 121, Issue 1 , Pages 5-10, January 2008