Coincident activation of Th2 T cells with onset of the disease and differential expression of GRO-gamma in peripheral blood leukocytes in minimal change disease

被引:12
作者
Adrogue, Horacio E.
Borillo, Jason
Torres, Lisa
Kale, Arundhati
Zhou, Cindy
Feig, Daniel
Merszei, Justin
Johnson, Richard
Lou, Ya-Huan
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Diagnost Sci DB, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Med, Houston, TX 77030 USA
[3] Methodist Hosp, Houston, TX 77030 USA
[4] Univ Florida, Dept Med, Gainesville, FL USA
关键词
minimal change disease; Th2 T cell activation; chemokine; growth related oncogene-gamma;
D O I
10.1159/000101371
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Involvement of Th2 T cells/NF kappa B in minimal change disease ( MCD) has been postulated. A promising but unconfirmed glomerular permeability factor ( GPF) from MCD T cells has been described. We explored whether GPF was the consequence of Th2 cell activation. Methods: Peripheral blood leukocytes ( PBL) from 16 MCD patients and 7 normal controls were analyzed and the results were statistically compared. Results: Flow cytometry demonstrated a significant expansion of CD4+ T cell population and dramatically increased CD69+ cells among CD4+ T cells in MCD, suggesting coincident activation of T cells with onset of the disease. RT-PCR on RNA from either freshly isolated PBL or post in vitro activation showed high-level expression of the Th2 cytokine interleukin-4 in all MCD patients. Importantly, both antibody microarray assay on sera and RT-PCR on mRNA of PBL revealed expression of a CXC chemokine GRO-gamma ( growth-related oncogene) in all MCD patients as compared with one of 7 controls. Conclusions: Our results reveal an association between onset of MCD and activation of Th2 cells. The GRO family has been implicated in the function of endothelial cells, and its expression is under NF kappa B regulation. Thus, GRO-gamma is a promising candidate for Th2-associated GPF in MCD. Copyright (C) 2007 S. Karger AG, Basel.
引用
收藏
页码:253 / 261
页数:9
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