Abstract | BACKGROUND: METHODS:
Nasal polyps were cultured in the presence of the cytokines described above and the concentration of eotaxin-2/CCL24 was measured in the culture supernatant. RESULTS:
IL-4 was found to be the major stimulus for eotaxin-2/CCL24 production from nasal polyps followed by IL-13 and IFN-gamma. IL-4 induced eotaxin-2/CCL24 in a dose-dependent manner with concentrations as low as 0.1 ng/ml being able to induce eotaxin-2/CCL24. By immunohistochemistry, eotaxin-2/CCL24 immunoreactivity was localized to mononuclear cells in the IL-4 stimulated nasal polyp tissue. Interestingly, nasal turbinates obtained from patients suffering from nonallergic rhinitis (vasomotor rhinitis) were also found to release eotaxin-2/CCL24 both spontaneously and following cytokine stimulation with IL-4 and IFN-gamma being major inducers of this cytokine. CONCLUSIONS:
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Authors | D Lezcano-Meza, B Dávila-Dávila, A Vega-Miranda, M C Negrete-García, L M Teran |
Journal | Allergy
(Allergy)
Vol. 58
Issue 10
Pg. 1011-7
(Oct 2003)
ISSN: 0105-4538 [Print] Denmark |
PMID | 14510718
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- CCL24 protein, human
- Chemokine CCL24
- Chemokines, CC
- Interleukin-13
- Interleukin-4
- Interferon-gamma
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Topics |
- Adult
- Cells, Cultured
- Chemokine CCL24
- Chemokines, CC
(biosynthesis, immunology)
- Dose-Response Relationship, Drug
- Female
- Humans
- Interferon-gamma
(pharmacology, physiology)
- Interleukin-13
(pharmacology, physiology)
- Interleukin-4
(pharmacology, physiology)
- Kinetics
- Leukocytes, Mononuclear
(immunology)
- Middle Aged
- Nasal Polyps
(immunology, pathology)
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