Concentration of interferon-inducible T cell chemoattractant and monocyte chemotactic protein-1 in serum and cerebrospinal fluid of patients with Lyme borreliosis.

S Grygorczuk, J Zajkowska, R Swierzbińska, S Pancewicz, M Kondrusik, T Hermanowska-Szpakowicz
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Abstract

Purpose: Chronic inflammation in Lyme borreliosis may be sustained by aberrant inflammatory response, characterized by Th1 lymphocyte predominance, which in turn may be determined by chemokines synthesized in inflammatory focus. The aim of the study was to evaluate synthesis of chemokines: interferon-induced T cell chemoattractant (I-TAC--chemoattractant for Th1 lymphocytes), and monocyte chemotactic protein (MCP-1) in Lyme borreliosis.

Material and methods: Study group consisted of 13 patients with erythema migrans, 10 with Lyme arthritis and 6 with neuroborreliosis. Serum, as well as cerebrospinal fluid (CSF) in neuroborreliosis, was obtained before (examination 1) and during (examination 2) antibiotic treatment. Control serum was obtained from 8 healthy volunteers and control csf from 8 patients in whom meningitis and neuroborreliosis was excluded after diagnostic lumbar puncture. The samples were assayed for MCP-1 and I-TAC by ELISA.

Results: Serum mean I-TAC concentration in examination 1 was 73.0 pg/ml in erythema migrans, 78.9 pg/ml in Lyme arthritis and 87.3 pg/ml in neuroborreliosis (29.9 pg/ml in controls, difference significant for neuroborreliosis) and did not change significantly in examination 2. MCP-1 serum concentration was significantly increased to 497.5 pg/ml in neuroborreliosis in examination 2. I-TAC concentration in csf remained low, while MCP-1 concentration in examination 1 was increased to 589.1 pg/ml, significantly higher than simultaneously in serum.

Conclusions: I-TAC synthesis is increased in Lyme borreliosis and may be a factor favoring predominance of Th1 lymphocyte subset. MCP-1 creates chemotactic gradient towards central nervous system and may contribute to csf pleocytosis in neuroborreliosis.

莱姆病患者血清和脑脊液中干扰素诱导T细胞趋化剂和单核细胞趋化蛋白-1的浓度变化。
目的:莱姆病的慢性炎症可能是由异常炎症反应持续的,其特征是Th1淋巴细胞优势,而Th1淋巴细胞优势又可能由炎症灶合成的趋化因子决定。该研究的目的是评估趋化因子的合成:干扰素诱导的T细胞趋化剂(I-TAC- Th1淋巴细胞的趋化剂)和单核细胞趋化蛋白(MCP-1)在莱姆病中的作用。材料与方法:研究组包括13例移行性红斑,10例莱姆病,6例神经螺旋体病。在(检查1)和(检查2)抗生素治疗期间检测血清和脑脊液(CSF)。对照血清来自8名健康志愿者,对照脑脊液来自8名诊断性腰椎穿刺后排除脑膜炎和神经螺旋体病的患者。ELISA法检测样品中MCP-1和I-TAC含量。结果:检查1中血清I-TAC平均浓度在移行性红斑组为73.0 pg/ml,莱姆病组为78.9 pg/ml,神经疏螺旋体病组为87.3 pg/ml(对照组为29.9 pg/ml,神经疏螺旋体病组差异有统计学意义),检查2无显著变化。检查2神经疏螺旋体病患者血清MCP-1浓度显著升高至497.5 pg/ml。试验1 MCP-1浓度升高至589.1 pg/ml,显著高于同期血清中MCP-1浓度。结论:莱姆病患者I-TAC合成增加,可能是Th1淋巴细胞亚群占优势的一个因素。MCP-1产生向中枢神经系统的趋化梯度,可能导致神经疏螺旋体病患者脑脊液多细胞增多。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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