Asthma and the Coronavirus Disease 2019 Pandemic: A Literature Review.

Even though respiratory viruses are one of the most common triggers for asthma exacerbations, not all of these viruses affect patients equally. There is no strong evidence supporting that patients with asthma have a higher risk of becoming seriously ill from coronavirus disease 2019 (CO-VID-19), although recent reports from the USA and the UK suggest that asthma is much more common in children and adults with mild to severe COVID-19 than has previously been reported in Asia and in Europe. As in previous severe acute respiratory syndrome (SARS) outbreaks, patients with asthma, especially children, appear to be less susceptible to the coronavirus with a low rate of asthma exacerbations. A different expression of viral receptors and T2 inflammation can be responsible for different outcomes. Future studies focused on asthma and on other allergic disorders are needed to provide a greater understanding of the impact of underlying asthma and allergic inflammation on COVID-19 susceptibility and disease severity. However, for the moment, it is crucial that asthmatic patients maintain their controller medication, from inhaled corticosteroids to biologics, without making any dose adjustments on their own or stopping the medication. New data are emerging daily, rapidly updating our understanding of this novel coronavirus.

Introduction

A new coronavirus (severe acute respiratory syndrome coronavirus 2; SARS-CoV-2) infection began to spread in Wuhan, China, in early December 2019 and has rapidly spread around the globe. The disease condition associated with this novel coronavirus is referred to as corona­virus disease 2019 (COVID-19), and this outbreak was ­declared a pandemic on March 11, 2020, by the World Health Organization (WHO) [1]. As of May 15, 2020, the outbreak had reached globally 4,580,498 confirmed cases and 305,618 deaths, and only 1,735,657 patients had recovered [2]. These numbers are much greater than those registered during the SARS and Middle East respiratory syndrome (MERS) pandemics, which occurred in 2003 and 2013, respectively [3], despite the fact that the COVID-19 mortality rate, to date, is lower [2, 3].

SARS-CoV-2 binds mainly to angiotensin converting enzyme 2 (ACE2) receptors in host cells which are abundant in the lungs, heart, blood vessels, and intestine and, after more than a decade of research, there are still no specific treatments or effective vaccines for coronavirus [3, 4, 5, 6].

COVID-19 presents with respiratory symptoms, from mild to severe, and a significant percentage of patients develop acute respiratory disease syndrome (ARDS); these severe symptoms are associated with a true cytokine storm, in particular IL-6, and death can be one of the outcomes [7].

Old age and underlying morbidities, such as cardiovascular diseases, in particular hypertension and metabolic disorders (obesity and diabetes), have been identified as significant risk factors for COVID-19 morbidity and mortality [7, 8, 9]. However, asthma and COPD may not be common comorbidities [10]. Moreover, the real impact of SARS-CoV-2 in asthma control is unclear.

Methods

A systematic search was carried out in the following 4 electronic databases: EMBASE, MEDLINE, MedRxiv, and Scopus to assess the relationship between asthma and COVID-10 using studies in the English language up to May 14, 2020. The search terms included were: “COVID-19” OR “SARS-CoV-2” OR “Coronavirus” AND “Asthma” OR “Allergy” OR “Case series” OR “Comorbidities” OR “Epidemiology” OR “Hospitalization” OR “Risk factors.” Additionally, the references of the initial included studies were hand searched to identify other possibly eligible studies.

Literature Review

Results from the first epidemiologic studies of the COVID-19 pandemic in China apparently did not identify asthma as a risk factor of severe COVID-19 [10, 11]. Of 171 children treated at Wuhan Children's Hospital (Wuhan, China), 3 (1.8%) required intensive care and mechanical ventilation; all of them had underlying diseases but there was no asthma reference [12]. The same data was found in a cross-sectional multicenter study carried out in 10 hospitals across Hubei province (China), including hospitalized children with COVID-19 [13] (Table 1).

Table 1

Asthma prevalence in COVID-19 studies

Study location	Reference	Country	Patients, n	COVID-19 population	Asthma prevalence, %
Children's Hospital, Wuhan	12	China	171	Hospitalized pediatric patients, 3 admitted to the ICU, mechanical ventilation	−
Hubei Province	13	China	25	Hospitalized pediatric patients, 2 received mechanical ventilation	−
Nationwide China	14	China	2,035	34.1% laboratory-confirmed cases; >90% asymptomatic to moderate cases.	−
Zhongnan Hospital of Wuhan	15	China	140	Hospitalized adult patients	−
Zhongnan Hospital of Wuhan	16	China	290	Hospitalized adult patients	0.3
Multicentric study, Wuhan	17	China	191	Hospitalized adult patients	−
Tongji Hospital of Wuhan	18	China	548	Hospitalized adult patients	0.9
Nationwide China	19	China	1,595	Adult patients with laboratory-confirmed cases, 16.0% severe cases and 3.2% mortality	−
19 Italian regions and 2 autonomous provinces	20	Italy	355	Adult patients, fatal cases	−
Lombardy region	21	Italy	1,591	Adult patients admitted to the ICU, 26% mortality	−
Confidence study	22	Italy	100	Pediatric emergency departments, mostly children with mild disease	−
La Paz Hospital	23	Spain	2,226	Hospitalized adult patients, 21% mortality	5.2
Catalonia region	24	Spain	124,190	Inpatients (14.6%) and outpatients	6.8
Lausanne University Hospital	25	Switzerland	200	Hospitalized adult patients, 18.5% on mechanical ventilation	4.0
Seattle Region	26	USA	12	Adult patients admitted to the ICU, 50% mortality	12.5
Evergreen Hospital, Washington	27	USA	21	Adult patients admitted to the ICU, 71% on mechanical ventilation, 67% mortality (24% of cases still admitted to the ICU)	9.5
COVID-19 in Children	28	USA	345	Pediatric patients, mild to severe	Asthma as most common comorbidity
Kaiser Permanente Northern California	29	USA	1,299	Adult patients, 29% hospitalized, 8.7% admitted to the ICU	7.4 (asthma/COPD)
COVID-NET, 14 states	30	USA	1,482	Hospitalized patients (74.5% aged ≥50 years)	17.0
Georgia, 8 hospitals	31	USA	305	Hospitalized adult patients (median age 60 years)	10.5
New York City area	32	USA	5,700	Adult (>99%) and pediatric hospitalized patients, 14.2% admitted to the ICU, 12.2% on mechanical ventilation, 21% died	9.0
Mount Sinai Hospitals, New York	33	USA	2,199	Hospitalized adult patients (median age 65 years), 36% admitted to the ICU, 29% died	8.2
New York-Presbyterian/Columbia University Irving Medical Center	34	USA	1,000	Adult hospitalized patients (85%), 27.7% of whom were admitted to the ICU	11.3
ISARIC study	35	UK	16,749	Hospitalized patients (median age 72 years, range 0−104 years)	14.0
OpenSAFELY case control populational study	36	UK	5,683	Fatal cases	Asthma with a higher risk of COVID-19 death; HR = 1.1−1.25 (no or recent use of OCS)
UK BioBank	37	UK	605	Hospitalized adult patients (median age 57.4 years)	17.9
Middle East region	39	Saudi Arabia	150	Hospitalized patients (median age 46 years), 10.7% admitted to the ICU	2.7
Epidemiological Surveillance System for Viral Respiratory Diseases of the Mexican Ministry of Health	40	Mexico	10,554	Patients with laboratory confirmed SARS-CoV-2, 39.4% were hospitalized and 9.2% were fatal cases	3.6

Dong et al. [14] (China), in a nationwide case series of 2,135 pediatric patients (mean age 7 years) with COVID-19, observed cases at the Chinese Center for Disease Control and Prevention from January 16, 2020, to February 8, 2020 (Hubei Province) and did not report any asthma case.

In a survey of 140 adult patients admitted with COVID-19 (China), the clinical characteristics and allergy status of the patients was investigated. All of the patients were community-acquired cases. Hypertension (30.0%) and diabetes mellitus (12.1%) were the most common comorbidities. Drug hypersensitivity (11.4%) and urticaria (1.4%) were self-reported by several patients. Asthma or other allergic diseases were not reported by any of the patients and the authors concluded that allergic diseases and asthma were not risk factors for SARS-CoV-2 infection. An older age and a high number of comorbidities, i.e., cardiovascular and metabolic diseases, were associated with COVID-19 severity [15]. The same authors studied a larger sample of 290 confirmed COVID-19 adult patients who were hospitalized, and they found only 1 patient with asthma (0.3%); once again, hypertension and diabetes mellitus were the most frequently found comorbidities [16].

In another retrospective, multicenter cohort study that included 191 adult inpatients with confirmed COVID-19 (Wuhan, China), 48% had at least 1 comorbid disease, with hypertension being the most common, followed by diabetes and coronary heart disease, with no asthma reference [17]. In a survey of 70 adult patients admitted with COVID-19 in Tongji Hospital (Wuhan, China), an asthma prevalence rate of 0.9% was found; this is markedly lower than that in the adult population in this region (6.4%) [18]. In this study, asthma was not identified as a risk factor for disease severity, in contrast with hypertension [18].

A nationwide analysis from China [19], including 1,590 COVID-19 cases from 575 hospitals in 31 provincial administrative regions, reported an overall rate of severe cases and mortality of 16.0 and 3.2%, respectively. The most prevalent comorbidity was hypertension (16.9%), followed by diabetes (8.2%). One hundred thirty (8.2%) patients reported having 2 or more comorbidities. None of the cases had physician-diagnosed asthma. After adjusting for age and smoking status, COPD (HR = 2.681; 95% CI 1.424–5.048), diabetes (HR = 1.59; 95% CI 1.03–2.45), hypertension (HR = 1.58; 95% CI 1.07–2.32), and malignancy (HR = 3.50; 95% CI 1.60–7.64) were identified as significant severity risk factors, including for intensive care unit (ICU) admission, mechanical ventilation, and death [19].

In Europe, in a sample of 355 patients with COVID-19 who died in Italy (with a mean age of 79.5 years) it was reported that comorbidities were associated with an increased mortality risk. Thirty percent of patients had ischemic heart disease, 35.5% had diabetes, 20.3% had active cancer, 24.5% had atrial fibrillation, 6.8% had dementia, and 9.6% had a history of stroke. Once again, no reference to chronic respiratory diseases was made, i.e., asthma or chronic obstructive pulmonary disease (COPD) [20].

Also in a retrospective case series of 1,591 consecutive patients with laboratory-confirmed COVID-19 admitted to ICU in 72 hospitals of the Lombardy Region in Italy between February 20 and March 18, 2020, 68% of the patients had at least 1 comorbidity. Hypertension was the most common comorbidity, affecting 49% of the 1,043 patients with available data. The second most common comorbidities were cardiovascular disease (21%) and hypercholesterolemia (18%). Only 4% had a history of COPD, with no reference to patients with asthma [21].

In the CONFIDENCE study[22] that included 100 pediatric COVID-19 cases also from Italy (median age 3.3 years; 58% with mild disease and only 1% with severe disease), there was no reference to chronic respiratory diseases as was found in previous pediatric Chinese surveys by Lu et al. [12] and Dong et al. [14].

Borobia et al. [23] from La Paz University Hospital, Madrid, Spain, in a sample of 2,226 adult patients (median age 61 years) admitted to hospital who either died (20.7%) or were discharged (79.3%), identified that the most common comorbidity was hypertension (41.3%), followed by other chronic cardiovascular diseases (19.3%) and diabetes (17.1%); asthma was identified in 5.2% of COVID-19 patients, with a lower prevalence rate of 3.7% in the fatal cases. COPD affected 6.9% of the population, with a prevalence of 14.1% in the fatal cases. Also from Spain, in Catalonia, Prieto-Alhambra et al. [24] analyzed a primary care database covering >6 million people, including 121,263 COVID-19 patients (both hospitalized and outpatients). Most common comorbidities were hypertension (24.3%) and obesity (19.9%). Asthma was present in 6.8% of the patients and COPD was found in 3.2%; 10.7% of all patients were treated with inhalers.

In 200 COVID-19 patients hospitalized in the Lausanne University Hospital, Switzerland, [25] an asthma prevalence rate of 4.0% was found; the asthma prevalence rate was 2.7% in those patients who required mechanical ventilation.

In the USA, Bhatraju et al. [26] (Seattle, WA, USA) reported 24 patients with COVID-19 admitted to the ICU with a mortality rate of 50%. As coexisting disorders, 58% had diabetes, 22% were current or former tobacco smokers, 21% had chronic kidney disease, and 14% had asthma, corresponding to 3 cases with mild asthma who had been treated with systemic corticosteroids in the week before ICU admission, as outpatients, for a presumed asthma exacerbation. These patients were subsequently admitted to the ICU with severe respiratory failure requiring invasive mechanical ventilation [26].

Arentz et al. [27] (WAUSA) described, in a case series, the characteristics and outcomes of 21 patients with COVID-19 admitted to the ICU at Evergreen Hospital, with a mean age of 70 years (range 43–92 years); the more common comorbidities identified were: chronic kidney disease (47.6%), congestive heart failure (42.9), diabetes (33.3%), and COPD (33.3%). Two patients had asthma (9.5%).

Data from the USA regarding 345 cases in children (<18 years) showed that 23% had at least 1 comorbidity [28]. Chronic respiratory diseases, i.e., asthma, were the most common associated diseases, although the authors did not quantify the prevalence. Comorbidities were more frequently present in pediatric patients who required hospitalization compared to those who were not admitted to hospital (77 vs. 12%), but there was no reference to asthma as a significant risk factor [28].

In a sample of 377 adult COVID-19 patients admitted to California (USA) hospitals, 7.4% had nondiscriminated asthma or COPD [29]. A data analysis of patients hospitalized in 14 states of the USA with COVID-19 during March 2020 (n = 1,482) [30] confirmed that hospitalization was much more frequent in adults (74.5% aged ≥50 years). Among patients with information on underlying conditions (n = 120), 89% had 1 or more comorbidities. The most common were hypertension and other cardiovascular diseases (77.5%), followed by obesity (48.3%) and diabetes mellitus (28.3%). Seventeen percent of the COVID-19-positive patients had asthma and 10.7% had COPD. According the Centers for Disease Control and Prevention (CDC) report, in admitted patients aged 18–49 years, obesity was the most prevalent underlying condition (59.0%), followed by asthma (27.3%) [30].

A report from 8 hospitals (Georgia, USA), also summarized medical data for 305 adult patients with confirmed COVID-19 who were admitted during March 2020. Overall, 225 (73.8%) patients had underlying conditions. Hypertension (67.5%), diabetes (39.7%), other cardiovascular diseases (25.6%) were found, as was severe obesity (BMI ≥40), which was present in 12.7% of patients. Asthma was identified in 10.5% of all of the patients (13.5% in patients aged 18–49 years, 13.1% in those aged 50–64 years, and 6.0% in those aged ≥65 years, with no statistically significant differences) and COPD in 5.2% [31].

In the large sample of hospitalized COVID patients (>99% adults), that included 5,700 patients hospitalized with COVID-19 in the New York City area (NY, USA), 14.2% were treated in the ICU, 12.2% received invasive mechanical ventilation, and 21% died [32]. An asthma prevalence was found in 9.0% (with no reference to asthma severity/control) and COPD was found in 5.4%; the most common comorbidities were hypertension (56.6%), obesity (41.7%), and diabetes (33.8%) [32].

In the NY Mount Sinai Hospitals, an 8.2% prevalence of asthma was found in 2,199 of hospitalized patients; it was not significantly different in those who died (7.4%) [33]. Also in NY (USA), in the first 1,000 consecutive adult patients with a positive SARS-CoV-2 PCR test who presented to the emergency department or were hospitalized at New York-Presbyterian/Columbia University Irving Medical Center between March 1 and April 5, 2020, an asthma prevalence of 11.3% was found; it was also not significantly different in those that were admitted to the ICU (12.3%) [34].

In the ISARICProspective Observational Cohort Study[35] with near real-time analysis, with the participation of 166 UK hospitals, 16,749 COVID-19 hospitalized patients were included between February 6 and April 18, 2020 (mostly adults). The commonest comorbidities were chronic cardiac disease (29%), uncomplicated diabetes (19%), non-asthmatic chronic pulmonary disease (19%), and asthma (14%); 47% had no documented reported comorbidity. Increased age and comorbidities including obesity were associated with a higher probability of mortality [35].

Very recent data from the OpenSAFELY Collaborative Study [36] identified asthma as a significant risk factor of death from COVID-19 in England (UK). The authors conducted a cohort study that included 17,425,445 adults using national primary care electronic health record data linked to in-hospital COVID-19 death data (from February 1, 2020, to April 25, 2020). An older age age was strongly associated with risk, with the age group ≥80 years having a more than 12-fold increased risk compared to those aged 50–59 years; most comorbidities were associated with a higher risk of COVID-19 hospital death, including asthma (fully adjusted HR = 1.11; 95% 1.02–1.20), with a greater HR for those with recent use of an oral corticosteroid (OCS) (HR = 1.25; 95% CI 1.08–1.44) [36].

Data from the UK Biobank [37], in a prospective case-control study, showed an asthma prevalence of 17.9% in 605 COVID-19 hospitalized patients, most of them adults (the asthma prevalence was of 13.5% in the control population) but the disease was not identified as an independent risk factor for COVID-19 hospitalization/severity, in contrast with hypertension and COPD. In the oldest population (age ≥65 years) included in the UK Biobank [38], the same tendency of asthma prevalence was found between hospitalized COVID-19 patients versus controls (18.2 vs. 13.0%), but again asthma was not identified as an independent risk factor for severity.

In a report from the Middle East (Saudi Arabia)[39] that included 150 hospitalized adult patients (mean age 46.1 years), it was found that 28.8 and 26.0% of the COVID-19 population had hypertension and diabetes, respectively. The asthma prevalence was 2.7%, and 1 patient with asthma was admitted to the ICU.

In a study aiming to estimate the risk factors for hospitalization and death in a Mexican population [40] infected with SARS-CoV-2 (n = 10,554, mean age 46.5 years; 39.4% hospitalized and 9.2% fatal cases), hypertension was the most prevalent comorbidity found (21.7%), followed by obesity (20.15%) and diabetes (17.7%). The asthma prevalence was 3.6% of this population (3.1% in the hospitalized patients and in 3.2% in the fatal cases). Patients with hypertension, obesity, and diabetes were more likely to be hospitalized and die than people without these comorbidities. Once again, asthma was not identified as an independent risk factor for hospitalization and/or mortality [40].

Discussion

Based on the available literature, there was no clear evidence that patients with asthma were at a higher risk of being infected or becoming severely ill with SARS-CoV-2, although recent reports from the USA and the UK suggest that asthma is much more common in children and adults with COVID-19 than was previously reported in Asia and in the first surveys in continental Europe.

Nevertheless, the prevalence of several underlying conditions identified in US hospitalized patients with COVID-19 was similar to those for hospitalized influenza patients during influenza seasons 2014–15 through 2018–19, i.e., regarding chronic respiratory diseases (29–31%) [41].

Of particular note in the UK is the association of asthma with a higher risk of COVID-19 hospital death, with the HR increasing further for those who received OCS, probably indicating a greater severity of disease. This contrasts with previous findings, in several countries, where asthma and other chronic respiratory diseases have been underrepresented in hospitalized patients [36]. Also in the UK asthma was reported in 14.0 and 17.9% of hospitalized patients but with no increased risk of death [35, 37].

Among school age children, viral infection reportedly accounts for up to 85% of asthma exacerbations, and viruses are more frequently isolated from symptomatic patients than from asymptomatic patients [42, 43]. Even though respiratory viruses are one of the most common triggers for asthma exacerbations in all age groups, not all of these viruses affect patients equally. In particular, the human rhinovirus was identified as the main individual contributor for asthma exacerbations, with coronavirus being one of the less identified triggers of asthma exacerbations in children as well as in adults [44]. A recent literature review concerning virus detection during asthma exacerbations confirmed that exacerbations were mainly associated with rhinovirus infection in all continents [45].

In previous SARS outbreaks, patients with asthma, in particular children, appeared to be less susceptible to the coronavirus, with a reported low rate of asthma exacerbations and a good prognosis on follow-up [10, 46]. In contrast, during influenza epidemics, asthma was associated with more severe disease, including the need for mechanical ventilation, not only in adults but also in children [47]. The exact reasons for this remain unknown, but it was confirmed during the current coronavirus pandemic [48].

From the recent COVID-19 literature, no definite conclusions can be drawn regarding asthma control or severity. Similarly, no information can be extrapolated about asthma phenotypes, i.e., regarding whether asthma is allergic or not.

COVID-19 outcomes vary from asymptomatic infection to death and it is possible that this clinical range reflects different airway levels of the SARS-CoV-2 receptor, ACE2, and the spike protein activator transmembrane protease serine 2 (TMPRSS2), considering that the virus cell entry also depends on S-protein priming by host cell proteases.

Blood eosinophil levels are a well-known predictor of airway T2 inflammation [49], and the measurement of blood eosinophil levels can be used as an accessible (not strong), proxy for investigation of the association between airway T2 inflammation and COVID-19 outcomes.

In early reports from China, a detailed clinical investigation of hospitalized COVID-19 cases suggested severe eosinopenia together with lymphopenia as a potential indicator of the diagnosis and to a worse prognosis, including death [15]. It was believed that low eosinophil counts in peripheral blood would be related to the SARS-CoV-2 infection itself. However, more recent studies from China and from Italy have not reported eosinopenia in patients with severe COVID-19 [26, 31, 50].

Although the relationship between eosinophil counts and COVID-19 is uncertain, attention is warranted to monitor eosinophil counts among patients with asthma who are using biological therapies that lead to decreased eosinophil counts and the clinical course of COVID-19 in cases infected with the SARS-CoV-2 [51].

Sajuthi et al. [52] studied in children the role of both T2 inflammation and viral infection in regulating the gene expression of ACE2 and TMPRSS2 and they found a strong influence of T2 cytokine-driven inflammation on both ACE2 (downregulation) and TMPRSS2 (upregulation) expression levels, which can have clinical implications for COVID-19 outcomes. In contrast, the authors found an equally strong positive influence of respiratory virus infections on ACE2 expression [52]. So, at least theoretically, in patients with asthma and high T2 inflammation, the consequence of an interferon-dependent inflammation requires close monitoring given the enhanced risk of complications due to SARS-CoV-2 infection.

A recent study that included asthma patients from 3 different cohorts of children and adults found that ACE2 receptor expression was lower in those patients with high allergic sensitization, but nonatopic asthma was not associated with this reduced expression [53]. These data suggest that this reduced ACE2 expression may be a potential contributor, among several other factors, of reduced COVID-19 severity in patients with respiratory allergies, i.e., allergic asthma [53].

Additionally, there is some early evidence coming from the Severe Asthma Research Program-3 (SARP), that inhaled corticosteroid therapy is also associated with reduction on ACE2 and TMPRSS2 gene expression from sputum [54]. These data stress the importance of maintain asthma controlled using the treatment according to the best practices, including with inhaled steroids.

There is also evidence to support that taking ICS may be beneficial in dealing coronavirus infections. In vitro studies have shown inhibitory actions of budesonide on coronavirus HCoV-229E replication and cytokine production [55], and preliminary not yet peer-reviewed data suggest that ciclesonide blocks SARS-CoV-2 ribonucleic acid replication [56] and inhibits its cytopathic activity [57], which may have clinical implications.

Although gene expression for ACE2 and TMPRSS2 did not differ in healthy and asthmatic patients, it was also found that males, African Americans, and patients with diabetes have increased expression of ACE2 and TMPRSS2 in their sputum cells, which may be associated with the poor prognosis of these patients when infected with the SARS-CoV-2 [54].

Dong et al. [58] very elegantly described selected cases of patients with COVID-19 (children and adults), demonstrating the profile complexity and different clinical presentations from mild to severe cases. Patients with common allergic diseases, such as rhinitis or atopic dermatitis, did not develop distinct symptoms or had severe courses, which may suggest a positive balance of type 2 immune regulation in COVID-19 pathogenesis.

New data are emerging daily, rapidly updating our understanding of this novel coronavirus, but it is crucial that patients with asthma and other allergic diseases such as allergic rhinitis maintain their controller medication, from inhaled corticosteroids to biologics [51, 59, 60], including allergen immunotherapy [61], without making any dose adjustments on their own or stopping medication, which may lead to a higher risk of asthma exacerbations, increased OCS use, and a higher probability of the need for emergency room access and hospitalization (risk factors for coronavirus exposure and spread). Likewise, it is important to maintain well-controlled rhinitis and rhinosinusitis, together with other known risk factors for asthma exacerbations [62].

The available data about OCS use in asthma exacerbations, though limited to 3 reported cases in mild asthmatics [26], are in accordance with data from previous coronavirus outbreaks, showing that systemic corticosteroids can be associated with a higher viral load [63, 64]. The UK data suggesting an increased death risk in patients with asthma, especially in those who recently received systemic steroids [36], stress that clinicians must be cautious and recognize the differences between hypoxic respiratory failure and bronchospasm to carefully balance the need for OCS prescription [51], and bronchodilators must be delivered by metered dose inhalers with spacers in order to prevent the viral spread related with nebulizer use [65].

As was shown by Kaye et al. [66], there is evidence of increased adherence to asthma (and COPD) pharmacologic treatment during the first months of COVID-19, which is encouraging and hopefully will have a positive effect on improvement of the control of asthma and minimize the need for acute care for this inflammatory chronic respiratory disease.

In conclusion, it is unclear whether patients with asthma are at a higher risk of developing COVID-19 and/or becoming severely ill. Future studies in all age groups are needed to provide a greater understanding of the impact of underlying asthma, other allergic diseases, and T2 inflammation on COVID-19 susceptibility and disease outcomes. The better we understand these interactions, the better we will be able protect the most vulnerable people, including those in high-risk groups.

Conflict of Interest Statement

The authors have no conflict of interests to declare related to this work.

Funding Sources

No funding was received for the publication of this paper.

Author Contributions

The named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship of this paper. M.M.-A. performed data extraction from the literature and drafted this paper. J.B. significantly contributed to the conception of and critically reviewed this paper. All of the authors reviewed and approved the final draft for publication.