Anti-IL-5 (mepolizumab) therapy induces bone marrow eosinophil maturational arrest and decreases eosinophil progenitors in the bronchial mucosa of atopic asthmatics
被引:222
作者:
Menzies-Gow, A
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机构:McMaster Univ, Dept Med, Hamilton, ON L8N 3Z5, Canada
Menzies-Gow, A
Flood-Page, P
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机构:McMaster Univ, Dept Med, Hamilton, ON L8N 3Z5, Canada
Flood-Page, P
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机构:
Sehmi, R
Burman, J
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机构:McMaster Univ, Dept Med, Hamilton, ON L8N 3Z5, Canada
Burman, J
Hamid, Q
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机构:McMaster Univ, Dept Med, Hamilton, ON L8N 3Z5, Canada
Hamid, Q
Robinson, DS
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机构:McMaster Univ, Dept Med, Hamilton, ON L8N 3Z5, Canada
Robinson, DS
Kay, AB
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机构:McMaster Univ, Dept Med, Hamilton, ON L8N 3Z5, Canada
Kay, AB
Denburg, J
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机构:McMaster Univ, Dept Med, Hamilton, ON L8N 3Z5, Canada
Denburg, J
机构:
[1] McMaster Univ, Dept Med, Hamilton, ON L8N 3Z5, Canada
[2] Univ London Imperial Coll Sci Technol & Med, Fac Med, Natl Heart & Lung Inst, London, England
[3] St Josephs Hosp, Firestone Inst Resp Hlth, Hamilton, ON, Canada
[4] Royal Brompton & Harefield NHS Trust, Dept Haematol, London, England
eosinophil progenitors;
bone marrow;
asthma;
anti-IL-5;
D O I:
10.1067/mai.2003.1382
中图分类号:
R392 [医学免疫学];
学科分类号:
100102 ;
摘要:
Background: Eosinophils develop from CD34(+) progenitors under the influence of IL-5. Atopic asthmatic individuals have increased numbers of mature eosinophils and eosinophil progenitors within their bone marrow and bronchial mucosa. We have previously reported that anti-IL-5 monoclonal antibody treatment decreases total bone marrow and bronchial mucosal eosinophil numbers in asthma. Objective: Using an anti-IL-5 monoclonal antibody, we examined the role of IL-5 in eosinophil development within the bone marrow and bronchial mucosa in asthma. Methods: Blood, bone marrow, and airway mucosal biopsy specimens were examined before and after anti-IL-5 (mepolizumab) treatment of asthmatic individuals in a double-blind, placebo-controlled trial. Numbers of mature and immature eosinophils were measured by histologic stain (bone marrow myelocytes, metamyelocytes, and mature eosinophils), flow cytometry (bone marrow and blood CD34(+)/IL-5Ralpha(+) cells), enumeration of bone marrow-derived eosinophil/basophil colony-forming units in methylcellulose culture, and sequential immunohistochemistry and in situ hybridization (bronchial mucosal CD34(+)/IL-5Ralpha mRNA(+) cells). Results: Mepolizumab decreased mature eosinophil numbers in the bone marrow by 70% (P = .017) in comparison with placebo and decreased numbers of eosinophil myelocytes and metamyelocytes by 37% (P = .006) and 44% (P = .003), respectively. However, mepolizumab had no effect on numbers of blood or bone marrow CD34(+), CD34(+)/IL-5Ra(+) cells, or eosinophil/basophil colony-forming units. There was a significant decrease in bronchial mucosal CD34(+)/IL-5Ralpha mRNA(+) c ell numbers in the anti-IL-5 treated group (P = .04). Conclusion: These data suggest that anti-IL-5 therapy might induce partial maturational arrest of the eosinophil lineage in the bone marrow. The reduction in airway CD34(+)/IL-5 mRNA(+) cell numbers suggests that IL-5 might also be required for local tissue eosinophilopoiesis.
机构:
Australian Natl Univ, Div Biochem & Mol Biol, John Curtin Sch Med Res, Canberra, ACT 0200, AustraliaAustralian Natl Univ, Div Biochem & Mol Biol, John Curtin Sch Med Res, Canberra, ACT 0200, Australia
Foster, PS
Hogan, SP
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机构:Australian Natl Univ, Div Biochem & Mol Biol, John Curtin Sch Med Res, Canberra, ACT 0200, Australia
Hogan, SP
Yang, M
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机构:Australian Natl Univ, Div Biochem & Mol Biol, John Curtin Sch Med Res, Canberra, ACT 0200, Australia
Yang, M
Mattes, J
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机构:Australian Natl Univ, Div Biochem & Mol Biol, John Curtin Sch Med Res, Canberra, ACT 0200, Australia
Mattes, J
Young, IG
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机构:Australian Natl Univ, Div Biochem & Mol Biol, John Curtin Sch Med Res, Canberra, ACT 0200, Australia
Young, IG
Matthaei, KI
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机构:Australian Natl Univ, Div Biochem & Mol Biol, John Curtin Sch Med Res, Canberra, ACT 0200, Australia
Matthaei, KI
Kumar, RK
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机构:Australian Natl Univ, Div Biochem & Mol Biol, John Curtin Sch Med Res, Canberra, ACT 0200, Australia
Kumar, RK
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Mahalingam, S
Webb, DC
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机构:Australian Natl Univ, Div Biochem & Mol Biol, John Curtin Sch Med Res, Canberra, ACT 0200, Australia
机构:
Australian Natl Univ, Div Biochem & Mol Biol, John Curtin Sch Med Res, Canberra, ACT 0200, AustraliaAustralian Natl Univ, Div Biochem & Mol Biol, John Curtin Sch Med Res, Canberra, ACT 0200, Australia
Foster, PS
Hogan, SP
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机构:Australian Natl Univ, Div Biochem & Mol Biol, John Curtin Sch Med Res, Canberra, ACT 0200, Australia
Hogan, SP
Yang, M
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机构:Australian Natl Univ, Div Biochem & Mol Biol, John Curtin Sch Med Res, Canberra, ACT 0200, Australia
Yang, M
Mattes, J
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机构:Australian Natl Univ, Div Biochem & Mol Biol, John Curtin Sch Med Res, Canberra, ACT 0200, Australia
Mattes, J
Young, IG
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机构:Australian Natl Univ, Div Biochem & Mol Biol, John Curtin Sch Med Res, Canberra, ACT 0200, Australia
Young, IG
Matthaei, KI
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机构:Australian Natl Univ, Div Biochem & Mol Biol, John Curtin Sch Med Res, Canberra, ACT 0200, Australia
Matthaei, KI
Kumar, RK
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机构:Australian Natl Univ, Div Biochem & Mol Biol, John Curtin Sch Med Res, Canberra, ACT 0200, Australia
Kumar, RK
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Mahalingam, S
Webb, DC
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机构:Australian Natl Univ, Div Biochem & Mol Biol, John Curtin Sch Med Res, Canberra, ACT 0200, Australia