Korean J Otolaryngol-Head Neck Surg.  1999 Jan;42(1):47-53.

Expression of RANTES mRNA in Early Recurrent Nasal Polyps

Affiliations
  • 1Department of Otolaryngology-Head and Neck Surgery, Korea University College of Medicine, Seoul, Korea. hakjung@netsgo.com
  • 2Hana Nose Institute, Seoul, Korea.

Abstract

BACKGROUND AND OBJECTIVES: RANTES is a powerful chemotactic and activating factor to some inflammatory cells including eosinophils, which represent the most abundant cell type among the numerous cellular infiltrates of nasal polyps. RANTES may have an important role in the recruitment of inflammatory cells during the development of nasal polyps. The purpose of this study is to investigate RANTES mRNA expression in nasal polyps, ethmoiditis mucosa and in the early recurrent nasal polyps in order to identify its role as a chemoattractant in recurrent nasal polyps. MATERIALS: Tissue samples of nasal polyps, ethmoiditis mucosa, and early recurrent nasal polyps were obtained from an endoscopic sinus surgery. For these samples, light microscopic examination for histopathology and RT-PCRs for RANTES mRNA expression were performed. Three normal ethmoidal mucosa and four hypertrophied inferior turbinates were also evaluated.
RESULTS
Tissue infiltration of eosinophils observed under the light microscope was in the following order: early recurrent nasal polyps (91%), nasal polyps (60%), and ethmoiditis mucosa (40%). About 97% of early recurrent nasal polyps showed RANTES mRNA expression, but nasal polyps and ethmoiditis mucosa showed 60% and 56% of expression rates.
CONCLUSION
The results suggest that RANTES may play an important role in the development of early recurrent nasal polyps undergoing active inflammatory reactions and the recruitment of some inflammatory cells including eosinophils. Further investigations for other chemokines related to eosinophils will provide better understanding of the mechanism in the formation of nasal polyps.

Keyword

Nasal polyp; RANTES; RT-PCR; Ethmoiditis

MeSH Terms

Chemokine CCL5*
Chemokines
Eosinophils
Mucous Membrane
Nasal Polyps*
RNA, Messenger*
Turbinates
Chemokine CCL5
Chemokines
RNA, Messenger
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