Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2019 Sep 2;8(9):1375.
doi: 10.3390/jcm8091375.

Severe Eosinophilic Asthma

Affiliations
Review

Severe Eosinophilic Asthma

Agamemnon Bakakos et al. J Clin Med. .

Abstract

Asthma is a heterogeneous disease with varying severity. Severe asthma is a subject of constant research because it greatly affects patients' quality of life, and patients with severe asthma experience symptoms, exacerbations, and medication side effects. Eosinophils, although at first considered insignificant, were later specifically associated with features of the ongoing inflammatory process in asthma, particularly in the severe case. In this review, we discuss new insights into the pathogenesis of severe asthma related to eosinophilic inflammation and the pivotal role of cytokines in a spectrum that is usually referred to as "T2-high inflammation" that accounts for almost half of patients with severe asthma. Recent literature is summarized as to the role of eosinophils in asthmatic inflammation, airway remodeling, and airway hypersensitivity. Major advances in the management of severe asthma occurred the past few years due to the new targeted biological therapies. Novel biologics that are already widely used in severe eosinophilic asthma are discussed, focusing on the choice of the right treatment for the right patient. These monoclonal antibodies primarily led to a significant reduction of asthma exacerbations, as well as improvement of lung function and patient quality of life.

Keywords: anti-IL-5; eosinophil; inflammation; interleukin-4; interleukin-5 (IL-5); severe asthma.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflicts of interest.

References

    1. Chung K.F., Wenzel S.E., Brozek J.L., Bush A., Castro M., Sterk P.J., Adcock I.M., Bateman E.D., Bel E.H., Bleecker E.R., et al. International ERS/ATS guidelines on definition, evaluation and treatment of severe asthma. Eur. Respir. J. 2014;43:343–373. doi: 10.1183/09031936.00202013. - DOI - PubMed
    1. Reddel H.K., Taylor D.R., Bateman E.D., Boulet L.-P., Boushey H.A., Busse W.W., Casale T.B., Chanez P., Enright P.L., Gibson P.G., et al. An official American Thoracic Society/European Respiratory Society statement: Asthma control and exacerbations: Standardizing endpoints for clinical asthma trials and clinical practice. Am. J. Respir. Crit. Care Med. 2009;180:59–99. doi: 10.1164/rccm.200801-060ST. - DOI - PubMed
    1. Bateman E.D., Boushey H.A., Bousquet J., Busse W.W., Clark T.J.H., Pauwels R.A., Pedersen S.E. Can guideline-defined asthma control be achieved? The Gaining Optimal Asthma ControL study. Am. J. Respir. Crit. Care Med. 2004;170:836–844. doi: 10.1164/rccm.200401-033OC. - DOI - PubMed
    1. Pavlidis S., Takahashi K., Kwong F.N.K., Xie J., Hoda U., Sun K., Elyasigomari V., Agapow P., Loza M., Baribaud F., et al. “T2-high” in severe asthma related to blood eosinophil, exhaled nitric oxide and serum periostin. Eur. Respir. J. 2019 doi: 10.1183/13993003.00938-2018. - DOI - PubMed
    1. Rothenberg M.E., Hogan S. The eosinophil. Annu. Rev. Immunol. 2006;24:147–174. doi: 10.1146/annurev.immunol.24.021605.090720. - DOI - PubMed

LinkOut - more resources