Role of local eosinophilopoietic processes in the development of airway eosinophilia in prednisone-dependent severe asthma

Summary Background In severe asthmatics with persistent airway eosinophilia, blockade of interleukin‐5 has significant steroid‐sparing effects and attenuates blood and sputum eosinophilia. The contribution of local maturational processes of progenitors within the airways relative to the recruitment...

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Published inClinical and experimental allergy Vol. 46; no. 6; pp. 793 - 802
Main Authors Sehmi, R., Smith, S. G., Kjarsgaard, M., Radford, K., Boulet, L.-P., Lemiere, C., Prazma, C. M., Ortega, H., Martin, J. G., Nair, P.
Format Journal Article
LanguageEnglish
Published England Blackwell Publishing Ltd 01.06.2016
Wiley Subscription Services, Inc
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Summary:Summary Background In severe asthmatics with persistent airway eosinophilia, blockade of interleukin‐5 has significant steroid‐sparing effects and attenuates blood and sputum eosinophilia. The contribution of local maturational processes of progenitors within the airways relative to the recruitment of mature cells from the peripheral circulation to the development of airway eosinophilia is not known. We hypothesize that local eosinophilopoiesis may be the predominant process that drives persistent airway eosinophilia and corticosteroid requirement in severe asthmatics. Objectives In a cross‐sectional study, the number and growth potential of eosinophil‐lineage‐committed progenitors (EoP) were assayed in 21 severe eosinophilic asthmatics, 19 mild asthmatics, eight COPD patients and eight normal subjects. The effect of anti‐IL‐5 treatment on mature eosinophils and EoP numbers was made in severe eosinophilic asthmatics who participated in a randomized clinical trial of mepolizumab (substudy of a larger GSK sponsored global phase III trial, MEA115575) where subjects received mepolizumab (100 mg, n = 9) or placebo (n = 8), as six monthly subcutaneous injections. Results Mature eosinophil and EoP numbers were significantly greater in the sputum of severe asthmatics compared with all other subject groups. In colony‐forming assays, EoP from blood of severe asthmatics demonstrated a greater response to IL‐5 than mild asthmatics. Treatment of severe asthmatics with mepolizumab significantly attenuated blood eosinophils and increased EoP numbers consistent with blockade of systemic eosinophilopoiesis. There was however no significant treatment effect on mature eosinophils, sputum EoP numbers or the prednisone maintenance dose. Conclusions and Clinical Relevance Patients with severe eosinophilic asthma have an exaggerated eosinophilopoeitic process in their airways. Treatment with 100 mg subcutaneous mepolizumab significantly attenuated systemic differentiation of eosinophils, but did not suppress local airway eosinophil differentiation to mature cells. Targeting IL‐5‐driven eosinophil differentiation locally within the lung maybe of relevance for optimal control of airway eosinophilia and asthma.
Bibliography:Father Sean O'Sullivan Postdoctoral Fellowship
GlaxoSmithKline
istex:8BCCA6C3EA2212C2ECE4743E18EF080F3FD01D37
Canada Research Chair in Airway Inflammometry
ark:/67375/WNG-LC2K52LF-5
Data S1. Figure S1. Figure S1. Study design: at baseline (Visit 1, screening pre-treatment time point) venous blood and sputum sampling were performed for progenitor and eosinophil enumeration. Figure S2. Sequential multi-gating strategy of sputum cells: (a) identification of HPC (CD34+45+ cells) using FlowJo software. Scatter plots show SSC and CD45 - region R1 identifies nucleated white blood cells (WBC). Region R2 identifies CD34+ marker. True CD34+ are further isolated based upon low granularity and low CD45+ marker expression-region R3. HPCs are characterized by medium size (medium FSC) and low granularity (low SSC) -region R4. (b) EoP are identified as HPC expressing CD125 compared to isotype control with a 98% confidence limit. (c) Further phenotyping of EoPs showing Lin- expression and co-expression of CD45RA, CD38 and CD123 was performed to confirm identification of eosinophil precursors as described by Mori et al. [12]. Figure S3. EoP clonogenic assay. Blood eosinophil progenitor cells (EoP) were enumerated by clonogenic expansion in methylcellulose culture. Compared to pre-treatment levels there was a trend for an increase in Eo/B-CFU grown with IL-5 (at 1 and 10 ng/ml) in the drug but not the placebo treated group. This suggests that inhibition of IL-5-driven terminal differentiation of eosinophils results in the increased circulating levels of EoP. Data with IL-5 at 0.1ng/ml is shown in Figure 4.
ArticleID:CEA12695
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
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ISSN:0954-7894
1365-2222
1365-2222
DOI:10.1111/cea.12695