Clinical significance of TLR3 and TLR4 in peripheral blood mononuclear cells from children with Henoch-Schönlein purpura nephritis.

Hong Chang,Zheng-Hai Qu,Na Cheng,Xiu-Qin Liu,Shou-Qing Zhang,Dong-Sheng Yu,Qiu-Ye Zhang

doi:10.3892/etm.2014.1638

Abstract

The aim of the present study was to investigate the expression levels and clinical significance of Toll-like receptor (TLR) 3 and 4 in peripheral blood mononuclear cells (PBMCs) collected from children with Henoch-Schönlein purpura (HSP) nephritis. The randomized controlled trial was conducted between August 2011 and March 2013, and 105 children with a clinical diagnosis of HSP were enrolled in the study. According to the 24-h urinary protein measurements and the presence of renal damage, the 105 cases were divided into groups A, B and C as follows: Group A, children with HSP but without renal damage; group B, children with HSP nephritis but without proteinuria; group C, children with HSP nephritis and proteinuria. A total of 30 healthy children were enrolled in the normal control group (group N). The primary endpoints were the detection of TLR3 and 4 mRNA and protein expression levels in PBMCs by flow cytometry and quantitative polymerase chain reaction. The mRNA and protein expression levels of TLR4 in the PBMCs were significantly higher in groups A, B and C when compared with group N. In addition, the mRNA and protein expression levels of TLR4 in group C were much higher when compared with groups A and B. A positive correlation was identified between TLR4 protein expression and 24-h urinary protein levels in group C. The expression levels of TLR3 did not significantly differ among the groups. Protein and mRNA expression levels of TLR4 in PBMCs significantly increased and exhibited a positive correlation with urinary protein excretion. These results indicate that aberrant activation of TLR4 may be relevant to the development of HSP nephritis.

Highlights

Secondary kidney damage is the most common complication in children with Henoch-Schönlein purpura (HSP) nephritis
These results indicate that aberrant activation of TLR4 may be relevant to the development of HSP nephritis
Expression of TLR3 and TLR4. mRNA expression levels of TLR4 were significantly higher in groups A, B and C when compared with group N (P

Summary

Introduction

Secondary kidney damage is the most common complication in children with Henoch-Schönlein purpura (HSP) nephritis. HSP is often considered to be preceded by an infection [1,2]; the cause of immunity function disorder remains unclear [3]. Allergic purpura is one of the most common types of vasculitis in children and mainly affects the vessels of the skin, gastrointestinal tract and kidneys. 20-60% of children with allergic purpura are complicated with renal damage, which is an important factor affecting the prognosis. Infection is the most important risk factor of HSP nephritis, of which the incidence is >70% [1,2]. Group A Streptococcus is the most common precipitant, demonstrable in up to one-third of cases, but exposure to Bartonella, Haemophilus parain‐ fluenza and numerous vaccines and drugs may precede the development of HSP. The role of microbial antigens in the pathogenesis of HSP remains elusive

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