Defective Functions of Circulating Cd4+Cd25+ and Cd4+Cd25- T Cells in Patients with Chronic Ordinary Urticaria
Resource
JOURNAL OF DERMATOLOGICAL SCIENCE v.51 n.2 pp.121-130
Journal
JOURNAL OF DERMATOLOGICAL SCIENCE
Journal Volume
v.51
Journal Issue
n.2
Pages
121-130
Date Issued
2008
Date
2008
Author(s)
CHEN, WU-CHARNG
CHIANG, BOR-LUEN
LIU, HSING-JIN EUGENE
LEU, SY-JYE
LEE, YUEH-LUN
Abstract
BACKGROUND: Patients with chronic ordinary urticaria (CU) are divided into two groups: 30-50% have chronic autoimmune urticaria, and the remainder have chronic idiopathic urticaria. CD4(+)CD25(+) regulatory T ( Treg) cells play critical roles in maintaining peripheral tolerance and preventing autoimmunity, but the characteristics of Treg cells have not yet been defined in CU. OBJECTIVE: To identify whether CD4(+) T cells play an important immunoregulatory role in the etiology of CU, we determined the frequencies and functions of circulating CD4(+)CD25(+) and CD4(+)CD25( -) T cells in CU patients and healthy control subjects, with special focus on the characteristics of CD4( +)CD25(+) T cells. METHODS: Peripheral blood mononuclear cells (PBMCs) were obtained from CU and healthy controls in this study. The frequency of CD4(+)CD25(+) T cells in PBMCs was detected by flow cytometry. The expression levels of forkhead box P3 (FOXP 3) and transforming growth factor-beta( TGF-beta) in CD4(+)CD25(+) T cells were detected by real- time PCR. Furthermore, the suppressive function of CD4(+)CD 25(+) T cells was analyzed. Additionally, the Th1/Th2 cytokine secretory profile in mitogen-stimulated CD4(+)CD25( -) T cells was measured by ELISA. RESULTS: An increased frequency of CD4(+)CD25(+) T cells was observed in CU patients (n=19) compared to control subjects (n=7 ). No significant difference was detected in the expression levels of FOXP 3 or TGF-beta between CU patients (n=14) and control subjects (n=7). Strikingly, the suppressive capacity of CD4 (+)CD25(+) Treg cells from 2 of 5 CU patients was partially defective. We also found that cytokine production from CD4(+ )CD25(-) T cells was significantly reduced in CU patients (n =9) compared to healthy donors (n=11). CONCLUSIONS: Our data demonstrate that CD4(+)CD25(+) and CD4(+)CD25(-) T cells in PBMCs exhibit defective functions in CU patients.
Subjects
chronic ordinary urticaria
CD4+CD25+ regulatory T cells
FOXP3
suppressive function
CD4+CD25- T cells
cytokines
Type
journal article