Literature DB >> 9739047

Circulating, but not local lung, IL-5 is required for the development of antigen-induced airways eosinophilia.

J Wang1, K Palmer, J Lŏtvall, S Milan, X F Lei, K I Matthaei, J Gauldie, M D Inman, M Jordana, Z Xing.   

Abstract

IL-5 is induced locally in the lung and systemically in the circulation during allergic airways eosinophilic inflammation both in humans and experimental animals. However, the precise role of local and systemic IL-5 in the development of allergic airways eosinophilia remains to be elucidated. In our current study, we demonstrate that compared with their IL-5(+/+) counterparts, IL-5(-/-) mice lacked an IL-5 response both in the lung and peripheral blood, yet they released similar amounts of IL-4, eotaxin, and MIP-1alpha in the lung after ovalbumin (OVA) sensitization and challenge. At cellular levels, these mice failed to develop peripheral blood and airways eosinophilia while the responses of lymphocytes, neutrophils, and macrophages remained similar to those in IL-5(+/+) mice. To dissect the relative role of local and systemic IL-5 in this model, we constructed a gene transfer vector expressing murine IL-5. Intramuscular IL-5 gene transfer to OVA-sensitized IL-5(-/-) mice led to raised levels of IL-5 compartmentalized to the circulation and completely reconstituted airways eosinophilia upon OVA challenge, which was associated with reconstitution of eosinophilia in the bone marrow and peripheral blood. Significant airways eosinophilia was observed for at least 7 d in these mice. In contrast, intranasal IL-5 gene transfer, when rendered to give rise to a significant but compartmentalized level of transgene protein IL-5 in the lung, was unable to reconstitute airways eosinophilia in OVA-sensitized IL-5(-/-) mice upon OVA-challenge, which was associated with a lack of eosinophilic responses in bone marrow and peripheral blood. Our findings thus provide unequivocal evidence that circulating but not local lung IL-5 is critically required for the development of allergic airways eosinophilia. These findings also provide the rationale for developing strategies to target circulating IL-5 and/or its receptors in bone marrow to effectively control asthmatic airways eosinophilia.

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Year:  1998        PMID: 9739047      PMCID: PMC509096          DOI: 10.1172/JCI2686

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  41 in total

1.  Antibody to interleukin-5 inhibits helminth-induced eosinophilia in mice.

Authors:  R L Coffman; B W Seymour; S Hudak; J Jackson; D Rennick
Journal:  Science       Date:  1989-07-21       Impact factor: 47.728

2.  A simple technique for the rescue of early region I mutations into infectious human adenovirus type 5.

Authors:  W J McGrory; D S Bautista; F L Graham
Journal:  Virology       Date:  1988-04       Impact factor: 3.616

3.  Expression of mRNA for interleukin-5 in mucosal bronchial biopsies from asthma.

Authors:  Q Hamid; M Azzawi; S Ying; R Moqbel; A J Wardlaw; C J Corrigan; B Bradley; S R Durham; J V Collins; P K Jeffery
Journal:  J Clin Invest       Date:  1991-05       Impact factor: 14.808

4.  Compartmentalized transgene expression of granulocyte-macrophage colony-stimulating factor (GM-CSF) in mouse lung enhances allergic airways inflammation.

Authors:  X F Lei; Y Ohkawara; M R Stämpfli; J Gauldie; K Croitoru; M Jordana; Z Xing
Journal:  Clin Exp Immunol       Date:  1998-08       Impact factor: 4.330

5.  Predominant TH2-like bronchoalveolar T-lymphocyte population in atopic asthma.

Authors:  D S Robinson; Q Hamid; S Ying; A Tsicopoulos; J Barkans; A M Bentley; C Corrigan; S R Durham; A B Kay
Journal:  N Engl J Med       Date:  1992-01-30       Impact factor: 91.245

6.  Effects of IL-5, granulocyte/macrophage colony-stimulating factor (GM-CSF) and IL-3 on the survival of human blood eosinophils in vitro.

Authors:  P C Tai; L Sun; C J Spry
Journal:  Clin Exp Immunol       Date:  1991-08       Impact factor: 4.330

7.  Transgenic mice expressing a hemopoietic growth factor gene (GM-CSF) develop accumulations of macrophages, blindness, and a fatal syndrome of tissue damage.

Authors:  R A Lang; D Metcalf; R A Cuthbertson; I Lyons; E Stanley; A Kelso; G Kannourakis; D J Williamson; G K Klintworth; T J Gonda
Journal:  Cell       Date:  1987-11-20       Impact factor: 41.582

8.  Recombinant human interleukin 5 is a selective eosinophil chemoattractant.

Authors:  J M Wang; A Rambaldi; A Biondi; Z G Chen; C J Sanderson; A Mantovani
Journal:  Eur J Immunol       Date:  1989-04       Impact factor: 5.532

9.  Eosinophilia in transgenic mice expressing interleukin 5.

Authors:  L A Dent; M Strath; A L Mellor; C J Sanderson
Journal:  J Exp Med       Date:  1990-11-01       Impact factor: 14.307

10.  Highly purified murine interleukin 5 (IL-5) stimulates eosinophil function and prolongs in vitro survival. IL-5 as an eosinophil chemotactic factor.

Authors:  Y Yamaguchi; Y Hayashi; Y Sugama; Y Miura; T Kasahara; S Kitamura; M Torisu; S Mita; A Tominaga; K Takatsu
Journal:  J Exp Med       Date:  1988-05-01       Impact factor: 14.307

View more
  20 in total

Review 1.  [Anti-interleukin-5 therapy for eosinophilic diseases].

Authors:  D Simon; L R Braathen; H-U Simon
Journal:  Hautarzt       Date:  2007-02       Impact factor: 0.751

2.  Haemopoietic mechanisms in murine allergic upper and lower airway inflammation.

Authors:  Jing Li; Hiroko Saito; Lynn Crawford; Mark D Inman; Michael M Cyr; Judah A Denburg
Journal:  Immunology       Date:  2005-03       Impact factor: 7.397

3.  Evidence for systemic rather than pulmonary effects of interleukin-5 administration in asthma.

Authors:  E L van Rensen; R G Stirling; J Scheerens; K Staples; P J Sterk; P J Barnes; K F Chung
Journal:  Thorax       Date:  2001-12       Impact factor: 9.139

4.  Recombinant adenovirus vectors expressing interleukin-5 and -6 specifically enhance mucosal immunoglobulin A responses in the lung.

Authors:  T A Braciak; W S Gallichan; F L Graham; C D Richards; A J Ramsay; K L Rosenthal; J Gauldie
Journal:  Immunology       Date:  2000-11       Impact factor: 7.397

5.  Single intranasal mucosal Mycobacterium bovis BCG vaccination confers improved protection compared to subcutaneous vaccination against pulmonary tuberculosis.

Authors:  Lihao Chen; Jun Wang; Anna Zganiacz; Zhou Xing
Journal:  Infect Immun       Date:  2004-01       Impact factor: 3.441

6.  Antigen and lipopolysaccharide play synergistic roles in the effector phase of airway inflammation in mice.

Authors:  Yong Woo Jung; Trenton R Schoeb; Casey T Weaver; David D Chaplin
Journal:  Am J Pathol       Date:  2006-05       Impact factor: 4.307

7.  Upregulated eotaxin expression and T cell infiltration in the basal and papillary epithelium in cows' milk associated reflux oesophagitis.

Authors:  A M Butt; S H Murch; C-L Ng; P Kitching; S M Montgomery; A D Phillips; J A Walker-Smith; M A Thomson
Journal:  Arch Dis Child       Date:  2002-08       Impact factor: 3.791

Review 8.  Current concepts of severe asthma.

Authors:  Anuradha Ray; Mahesh Raundhal; Timothy B Oriss; Prabir Ray; Sally E Wenzel
Journal:  J Clin Invest       Date:  2016-07-01       Impact factor: 14.808

9.  Biodegradable antigen-associated PLG nanoparticles tolerize Th2-mediated allergic airway inflammation pre- and postsensitization.

Authors:  Charles B Smarr; Woon Teck Yap; Tobias P Neef; Ryan M Pearson; Zoe N Hunter; Igal Ifergan; Daniel R Getts; Paul J Bryce; Lonnie D Shea; Stephen D Miller
Journal:  Proc Natl Acad Sci U S A       Date:  2016-04-18       Impact factor: 11.205

10.  Pulmonary eosinophilia requires interleukin-5, eotaxin-1, and CD4+ T cells in mice immunized with respiratory syncytial virus G glycoprotein.

Authors:  Teresa R Johnson; Marc E Rothenberg; Barney S Graham
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