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Blood Leukocyte Profiling in Eosinophilic Type 2 Asthma: Influence of Systemic IL-5 Targeting

Recruiting
Conditions
Asthma
Interventions
Biological: Mepolizumab
Drug: Standard inhaled corticosteroids (ICS) and long-acting beta 2 agonists (LABA)
Registration Number
NCT05689931
Lead Sponsor
Region Skane
Brief Summary

The goal of this exploratory and observational prospective study is to study the composition and phenotypes of blood leukocytes collected from asthmatic patients before and after instantiated treatment with the interleukin-5 neutralizing antibody mepolizumab. Comparisons will be made to leukocyte profiles in patients already on mepolizumab treatment, asthma patients without any biological treatment, and non-diseased control subjects.

Detailed Description

Asthma is a chronic inflammatory and obstructive condition affecting the airways. The disease is commonly associated with elevated blood eosinophils and tissue eosinophilia. Many aspects of the pathophysiological mechanisms and clinical symptoms are controlled by conventional therapies such as inhaled corticosteroids (ICS) and long acting β2 agonists. However, some patients remain clinically uncontrolled and need additional treatment such as direct targeting of eosinophil granulocytes by neutralizing the eosinophil-promoting cytokine interleukin 5 (IL5). Mepolizumab is a humanized monoclonal IL-5 neutralizing antibody that is used to treat patients with moderate-severe eosinophilic asthma. While a marked reduction of eosinophils is a key effect of mepolizumab, the exact mechanism of action is unknown. Apart from basophils, that also express the receptor for IL-5, other leukocytes are likely to be indirectly affected by the suppressed eosinophilia. In addition, it is largely unknown to what extent the few eosinophils remaining after anti-IL5 treatment differ from pre-treatment eosinophils.

The present study is a prospective observational asthma study that aims to use microscopic analysis to investigate the composition and subtypes of blood leukocytes collected before and after instantiated mepolizumab treatment. Comparisons are made to patients already on mepolizumab treatment, asthma patients without any biological treatment, and non-diseased control subjects.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
80
Inclusion Criteria
  • Clinical diagnosis of asthma (the asthma patient arms)
  • Eligible for Mepolizumab treatment as per the country-specific prescribing information (the arms with Mepolizumab)

Exclusion criteria:

  • Any diagnosed infection (all arms)
  • Previous history of lung disease, chronic inflammatory condition, atopy, or cardiovascular disease. Diagnosed or perceived infection within 3 weeks prior to blood sampling (Healthy non-asthma control subjects)
Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Asthma patients initiating Mepolizumab treatmentStandard inhaled corticosteroids (ICS) and long-acting beta 2 agonists (LABA)Patients will be selected on the standard criteria used to select eligible asthma patients for mepolizumab treatment (i.e. patients with eosinophilic asthma that are not controlled by conventional high dose ICS and LABA etc). All eligible asthma patients may be included. Exclusion criteria: any infection
Asthma patients already on Mepolizumab treatmentStandard inhaled corticosteroids (ICS) and long-acting beta 2 agonists (LABA)Patients that have been selected and given Mepolizumab treatment for \> 4 months according to standard eligible and treatment regimen criteria (i.e. patients with eosinophilic asthma that are not controlled by conventional high dose ICS and LABA etc). All eligible asthma patients that have been on Mepolizumab treatment for \> 4 weeks will be included. Exclusion criteria: any infections
Asthma patients initiating Mepolizumab treatmentMepolizumabPatients will be selected on the standard criteria used to select eligible asthma patients for mepolizumab treatment (i.e. patients with eosinophilic asthma that are not controlled by conventional high dose ICS and LABA etc). All eligible asthma patients may be included. Exclusion criteria: any infection
Asthma patients already on Mepolizumab treatmentMepolizumabPatients that have been selected and given Mepolizumab treatment for \> 4 months according to standard eligible and treatment regimen criteria (i.e. patients with eosinophilic asthma that are not controlled by conventional high dose ICS and LABA etc). All eligible asthma patients that have been on Mepolizumab treatment for \> 4 weeks will be included. Exclusion criteria: any infections
Asthma patients without Mepolizumab treatmentStandard inhaled corticosteroids (ICS) and long-acting beta 2 agonists (LABA)Inclusion: Asthma patients without any biological (antibody-based) treatment but on routine ICS and LABA treatment as part of their normal care. Exclusion criteria are any infections
Primary Outcome Measures
NameTimeMethod
Change in Blood Basophil Marker ExpressionChange from baseline at 1-3 days, 1 week, 4 weeks, and 4 months after initiated biological treatment

Quantitative immunohistochemical analysis of basophil marker expression in blood leukocyte pellets

Change in Blood Eosinophil Marker ExpressionChange from baseline at 1-3 days, 1 week, 4 weeks, and 4 months after initiated biological treatment

Quantitative immunohistochemical analysis of eosinophil marker expression in blood leukocyte pellets

Change in Blood Leukocyte CompositionChange from baseline at 1-3 days, 1 week, 4 weeks, and 4 months after initiated biological treatment

Immunohistochemical determination of the relative proportion (percent) of the leukocyte populations in blood leukocyte pellets

Secondary Outcome Measures
NameTimeMethod
Change in Blood T Lymphocyte Marker ExpressionChange from baseline at 1-3 days, 1 week, 4 weeks, and 4 months after initiated biological treatment

Quantitative immunohistochemical analysis of T lymphocyte marker expression in paraffin-embedded blood leukocyte pellets

Change in Blood B Lymphocyte Marker ExpressionChange from baseline at 1-3 days, 1 week, 4 weeks, and 4 months after initiated biological treatment

Quantitative immunohistochemical analysis of T lymphocyte marker expression in paraffin-embedded blood leukocyte pellets

Leukocyte Total Cell CountsChange from baseline at 1-3 days, 1 week, 4 weeks, and 4 months after initiated biological treatment

Routine hemacytometer total leukocyte cell counts

Trial Locations

Locations (1)

The Lung and Allergy Clinic, Skåne University Hospital (SUS)

🇸🇪

Lund, Skane, Sweden

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