Hostname: page-component-848d4c4894-nr4z6 Total loading time: 0 Render date: 2024-05-24T03:29:26.081Z Has data issue: false hasContentIssue false
  • English
  • Français

Th1 and Th2 CD4+ T cells and Tc1 and Tc2 CD8+ T cells of patients with Wegener’s granulomatosis

Published online by Cambridge University Press:  08 March 2006

Nobuo Ohta ,
Shigeru Fukase ,
Takeo Fuse  and
Masaru Aoyagi
Nobuo Ohta
Affiliation:
Department of Otolaryngology, Yamagata University School of Medicine, Yamagata, Japan.
Shigeru Fukase
Affiliation:
Department of Otolaryngology, Yamagata University School of Medicine, Yamagata, Japan.
Takeo Fuse
Affiliation:
Department of Otolaryngology, Yamagata University School of Medicine, Yamagata, Japan.
Masaru Aoyagi
Affiliation:
Department of Otolaryngology, Yamagata University School of Medicine, Yamagata, Japan.
Get access Rights & Permissions [Opens in a new window]

Abstract

A Th1/Th2 cytokine imbalance with a predominance of Th1 cytokines has been suggested to be of pathogenic importance in Wegener’s granulomatosis. To evaluate the role of Th1/Th2 cytokines in Wegener’s granulomatosis, the subsets of Th1, Th2, Tc1 and Tc2 cells from patients with active Wegener’s granulomatosis were examined by intracellular cytokine flow cytometry. The population of Tc1 cells (72.0 ± 14.4 per cent) in Wegener’s granulomatosis was significantly increased compared with Tc1 cells (37.3 ± 14.6 per cent) in control (p<0.05). Th1, Th2 and Tc2 cells in Wegener’s granulomatosis were not significantly increased compared with the control cells. These results indicate that the predominance of Tc1 cells might contribute to the mechanism of the pathogenesis of Wegener’s granulomatosis.

Keywords

CytokinesWegener’s GranulomatosisFlow Cytometry
Type
Research Article
Information
The Journal of Laryngology & Otology , Volume 116 , Issue 8 , August 2002 , pp. 605 - 609
Copyright
© Royal Society of Medicine Press Limited 2002

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)