The JI
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     
 


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Jahnsen, F. L.
Right arrow Articles by Johansen, F.-E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Jahnsen, F. L.
Right arrow Articles by Johansen, F.-E.
The Journal of Immunology, 1999, 163: 1545-1551.
Copyright © 1999 by The American Association of Immunologists

Glucocorticosteroids Inhibit mRNA Expression for Eotaxin, Eotaxin-2, and Monocyte-Chemotactic Protein-4 in Human Airway Inflammation with Eosinophilia1

Frode L. Jahnsen2,*, Rolf Haye{dagger}, Einar Gran{dagger}, Per Brandtzaeg* and Finn-Eirik Johansen*

* Laboratory for Immunohistochemistry and Immunopathology (LIIPAT), Institute of Pathology, and {dagger} Department of Ear, Nose, and Throat, University of Oslo, The National Hospital, Rikshospitalet, Oslo, Norway

How eosinophils are preferentially recruited to inflammatory sites remains elusive, but increasing evidence suggests that chemokines that bind to the CCR3 participate in this process. In this study, we investigated the transcript levels and chemotactic activity of CCR3-binding chemokines in nasal polyps, a disorder often showing prominent eosinophilia. We found that mRNA expression for eotaxin, eotaxin-2, and monocyte-chemotactic protein-4 was significantly increased in nasal polyps compared with turbinate mucosa from the same patients, or histologically normal nasal mucosa from control subjects. Interestingly, the novel CCR3-specific chemokine, eotaxin-2, showed the highest transcript levels. Consistent with these mRNA data, polyp tissue fluid exhibited strong chemotactic activity for eosinophils that was significantly inhibited by a blocking Ab against CCR3. When patients were treated systemically with glucocorticosteroids, the mRNA levels in the polyps were reduced to that found in turbinate mucosa for all chemokines. Together, these findings suggested an important role for CCR3-binding chemokines in eosinophil recruitment to nasal polyps. Such chemokines, therefore, most likely contribute significantly in the pathogenesis of eosinophil-related disorders; and the reduced chemokine expression observed after steroid treatment might reflect, at least in part, how steroids inhibit tissue accumulation of eosinophils.




This article has been cited by other articles:


Home page
IOVSHome page
N. Hashida, N. Ohguro, K. Nakai, M. Kobashi-Hashida, S.-i. Hashimoto, K. Matsushima, and Y. Tano
Microarray Analysis of Cytokine and Chemokine Gene Expression after Prednisolone Treatment in Murine Experimental Autoimmune Uveoretinitis
Invest. Ophthalmol. Vis. Sci., November 1, 2005; 46(11): 4224 - 4234.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
H. Schjerven, P. Brandtzaeg, and F.-E. Johansen
Hepatocyte NF-1 and STAT6 Cooperate with Additional DNA-Binding Factors to Activate Transcription of the Human Polymeric Ig Receptor Gene in Response to IL-4
J. Immunol., June 15, 2003; 170(12): 6048 - 6056.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Respir. Crit. Care Med.Home page
A. Kibe, H. Inoue, S. Fukuyama, K. Machida, K. Matsumoto, H. Koto, T. Ikegami, H. Aizawa, and N. Hara
Differential Regulation by Glucocorticoid of Interleukin-13-induced Eosinophilia, Hyperresponsiveness, and Goblet Cell Hyperplasia in Mouse Airways
Am. J. Respir. Crit. Care Med., January 1, 2003; 167(1): 50 - 56.
[Abstract] [Full Text] [PDF]


Home page
FASEB J.Home page
J. GALON, D. FRANCHIMONT, N. HIROI, G. FREY, A. BOETTNER, M. EHRHART-BORNSTEIN, J. J. O'SHEA, G. P. CHROUSOS, and S. R. BORNSTEIN
Gene profiling reveals unknown enhancing and suppressive actions of glucocorticoids on immune cells
FASEB J, January 1, 2002; 16(1): 61 - 71.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Respir. Cell Mol. Bio.Home page
C. Bandeira-Melo, A. Herbst, and P. F. Weller
Eotaxins . Contributing to the Diversity of Eosinophil Recruitment and Activation
Am. J. Respir. Cell Mol. Biol., June 1, 2001; 24(6): 653 - 657.
[Full Text] [PDF]


Home page
J. Immunol.Home page
H. Schjerven, P. Brandtzaeg, and F.-E. Johansen
Mechanism of IL-4-Mediated Up-Regulation of the Polymeric Ig Receptor: Role of STAT6 in Cell Type-Specific Delayed Transcriptional Response
J. Immunol., October 1, 2000; 165(7): 3898 - 3906.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Respir. Crit. Care Med.Home page
B. LAMKHIOUED, E. A. GARCIA-ZEPEDA, S. ABI-YOUNES, H. NAKAMURA, S. JEDRZKIEWICZ, L. WAGNER, P. M. RENZI, Z. ALLAKHVERDI, C. LILLY, Q. HAMID, et al.
Monocyte Chemoattractant Protein (MCP)-4 Expression in the Airways of Patients with Asthma . Induction in Epithelial Cells and Mononuclear Cells by Proinflammatory Cytokines
Am. J. Respir. Crit. Care Med., August 1, 2000; 162(2): 723 - 732.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
This Website Copyright © 1999 by The American Association of Immunologists, Inc. All rights reserved.
All Contents Copyright © 1999 by The American Association of Immunologists, Inc. All rights reserved.