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What is Eosinophilic asthma?

Eosinophilic asthma (EA) is characterized by severe, chronic disease. Approximately 10% of all cases of asthma are defined as severe, and nearly half of those with severe asthma have signs of EA. The disease typically has an onset in adulthood, with diagnosis peaking in adults aged 35-50. While most asthma results from allergy or occurs with other allergic type conditions (e.g., hay fever, food allergy, eczema, or other allergic conditions), this does not appear to be the case with EA. Symptoms of EA not only include the typical asthma symptoms of shortness of breath, wheezing and coughing, but also chronic sinus infections and nasal polyps.

How is Eosinophilic asthma diagnosed?

The diagnosis of EA can be made through the finding of elevated eosinophils in blood, sputum and in bronchial biopsy. Elevated level of eosinophils is associated with chronic inflammation, obstruction and remodeling in airways resulting in more severe symptoms and more frequent exacerbations. It has also been found that the level of eosinophils in both sputum and blood correlates with the severity of asthma and prognosis. [Schleich 2014] These elevated levels of eosinophils can be seen despite standard corticosteroid treatment, especially among African Americans. [Nyenhuis 2017]

What are the latest treatments for Eosinophilic asthma?

Treatment of EA includes the standard asthma therapies, such as bronchodilators and corticosteroid treatment. Approximately 10-20% of those who are treated with these standard therapeutics continue to have poorly controlled asthma. [Walford 2014] There is emerging evidence that treatment regimens may have varying efficacy based on demographic characteristics, and that these varying responses may have a genetic component. [Levin 2019] A recent clinical study found that African American treated with inhaled corticosteroids have greater eosinophilic airway inflammation as compared to other asthma patients treated with inhaled corticosteroids. This marker of chronic inflammation and disease severity may help explain the greater asthma burden among African Americans. [Nyenhuis 2017] In the treatment of EA, biologics that can be used in combination with standard therapies in refractory disease have been developed. In EA, inflammation mediators, such as interleukin-5, have been targeted by newer therapeutics, as IL-5 plays a key role in the differentiation, survival, migration, and activation of eosinophils. In recent years, two monoclonal antibodies (mepolizumab and reslizumab) which target IL-5 and one that targets a subunit of the IL-5 receptor (benralizumab) have been developed and approved for the treatment of EA.

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What is the risk level for Eosinophilic asthma?

Asthma is a burdensome disease and is associated with higher healthcare costs, decreased quality of life and higher mortality rates. This is particularly true for those with severe asthma and racial minorities. [Hossny 2017; Moorman 2007] African Americans have been found to be more likely to have uncontrolled asthma and reduced lung function as compared to Caucasian patients [Nyenhuis 2017], as well as being more likely to experience asthma-related hospitalizations, emergency department visits and mortality. [Moorman 2007] African Americans not only have a higher prevalence of asthma, but have higher rates of morbidity and mortality, with nearly 2 to 3 times the mortality rates as compared with Caucasians. [Akinbami 2006] Even after controlling for factors such as environmental exposure, disease severity and access to healthcare, African Americans with asthma have still been found to have higher rates of morbidity and mortality. [Ford 2006] It is thought that these signs of severe, refractory disease among African Americans with asthma may in part be linked to increased levels of eosinophilic airway inflammation.


Akinbami L. Asthma prevalence, health care use and mortalitiy: United States 2003–05. CDC National Center for Health Statistics; 2006.

Ford JG, McCaffrey L. Understanding disparities in asthma outcomes among. African Americans Clinics in Chest Medicine. 2006;27(3):423–430.

Hossny E, Caraballo L, Casale T, El-Gamal Y, Rosenwasser L. Severe asthma and quality of life. World Allergy Organ J. 2017;10(1):28.

Levin AM, et al. Integrative approach identifies corticosteroid response variant in diverse populations with asthma. Journal of Allergy and Clinical Immunology, Volume 143, Issue 5, 1791 – 1802.

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Moorman JE, Rudd RA, Johnson CA, King M, Minor P, Bailey C, et al. National Surveillance for Asthma—United States, 1980–2004. MMWR Surveillance Summary. 2007;56(8):1–54.

Nyenhuis SM, Krishnan JA, Berry A, et al. Race is associated with differences in airway inflammation in patients with asthma. J Allergy Clin Immunol. 2017;140(1):257–265.e11.

Schleich FN, Chevremont A, Paulus V, et al. Importance of concomitant local and systemic eosinophilia in uncontrolled asthma. Eur Respir J 2014; 44: 97–108.

Walford HH, Doherty TA. Diagnosis and management of eosinophilic asthma: a US perspective. J Asthma Allergy. 2014;7:53–65.