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I 型免疫反应细胞因子-趋化因子级联反应与肺动脉高压有关。

Type I immune response cytokine-chemokine cascade is associated with pulmonary arterial hypertension.

机构信息

Division of Pulmonary, Critical-Care, Allergy & Immunology; David Geffen School of Medicine, Ronald Reagan-University of California Los Angeles Medical Center, CA 90095, USA.

出版信息

J Heart Lung Transplant. 2012 Aug;31(8):865-73. doi: 10.1016/j.healun.2012.04.008. Epub 2012 May 30.

DOI:10.1016/j.healun.2012.04.008
PMID:22658713
Abstract

BACKGROUND

Perivascular infiltrating mononuclear cells have been described in the vasculopathy found in multiple types of pulmonary arterial hypertension (PAH). We determined the expression of a specific type 1 immune response cytokine-chemokine cascade-interleukin (IL)-18 → (monokine induced by γ-interferon [MIG]/chemokine [C-X-C motif] ligand [CXCL] 9, interferon γ-induced protein [IP]-10/CXCL10 and interferon-inducible T-cell α chemoattractant [ITAC]/CXCL11)-in plasma samples from individuals with World Health Organization (WHO) Group 1 PAH.

METHODS

We analyzed cytokine and chemokine protein levels in plasma from 43 individuals with WHO Group 1 PAH by enzyme-linked immunosorbent assay compared with 35 healthy individuals. Immunohistochemical studies on tissue specimens from WHO Group 1 PAH patients were performed for cytokines and chemokines and their respective receptors.

RESULTS

Plasma IL-18 levels from WHO Group 1 PAH patients were significantly increased compared with healthy controls. Downstream chemokine CXCL10, but not CXCL9 or CXCL11, was markedly elevated compared with controls. Cellular sources of IL-18 were medial but not intimal smooth muscle cells. IL-18Rα was expressed from medial smooth muscle cells, endothelial cells, and mononuclear cells. CXCL10 and its main receptor, CXCR3, were expressed from infiltrating vascular wall mononuclear cells.

CONCLUSIONS

These data suggest that augmented expression of IL-18 and CXCL10 may perpetuate an inflammatory milieu that eventually contributes to the vascular obstruction characteristic of PAH.

摘要

背景

在多种肺动脉高压(PAH)中发现的血管病变中,已有血管周围浸润的单核细胞的描述。我们确定了特定的 1 型免疫反应细胞因子-趋化因子级联反应-白细胞介素(IL)-18→(γ干扰素诱导的单核细胞因子[MIG]/趋化因子[C-X-C 基序]配体[CXCL]9、干扰素γ诱导蛋白[IP]-10/CXCL10 和干扰素诱导的 T 细胞α趋化因子[ITAC]/CXCL11)在 1 型世界卫生组织(WHO)PAH 患者的血浆样本中的表达。

方法

我们通过酶联免疫吸附试验分析了 43 名 1 型 WHO PAH 患者和 35 名健康对照者血浆中细胞因子和趋化因子的蛋白水平。对 1 型 WHO PAH 患者的组织标本进行细胞因子和趋化因子及其相应受体的免疫组织化学研究。

结果

与健康对照组相比,1 型 WHO PAH 患者的血浆 IL-18 水平显著升高。下游趋化因子 CXCL10 而非 CXCL9 或 CXCL11 与对照组相比明显升高。IL-18 的细胞来源为中膜而非内膜平滑肌细胞。IL-18Rα 在内膜平滑肌细胞、内皮细胞和单核细胞中表达。CXCL10 及其主要受体 CXCR3 表达于浸润的血管壁单核细胞。

结论

这些数据表明,IL-18 和 CXCL10 的表达增加可能使炎症环境持久存在,最终导致 PAH 特征性的血管阻塞。

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