巨噬细胞特异性受体CD163在炎性疾病中的诊断和预后潜力

Christa Buechler, Kristina Eisinger, Sabrina Krautbauer
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引用次数: 62

摘要

CD163是血红蛋白和血红蛋白/接触珠蛋白复合物内吞作用的清道夫受体,几乎只在单核细胞和巨噬细胞上表达。CD163是由IL-10和糖皮质激素诱导的,而TNF等促炎细胞因子则降低其表达。细胞因子IL-6根据激活的信号通路发挥促炎和抗炎作用,强烈上调CD163。参与炎症下调的抗炎细胞表达高CD163,控制免疫反应。toll样受体2、4和5的配体刺激CD163的外结构域脱落,从而释放可溶性CD163 (sCD163),介导游离血红蛋白的细胞摄取。可溶性CD163在血液中循环,并在危重病人、慢性炎症和感染性疾病的血清中升高。血清sCD163浓度与疾病严重程度相关,是几种炎症性疾病的诊断、预后和治疗药物监测的合适生物标志物。升高的sCD163甚至可以预测某些疾病的合并症和死亡率。CD163/sCD163与疾病严重程度的关系表明单核/巨噬细胞在多种疾病中的重要作用。CD163是一种特异性地将药物递送到巨噬细胞的靶标,旨在提高治疗效率和减少不良反应。本文就CD163表达和脱落的调控因子、CD163和sCD163的功能以及CD163和/或sCD163主要升高的炎症性疾病进行综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diagnostic and prognostic potential of the macrophage specific receptor CD163 in inflammatory diseases.

CD163 is a scavenger receptor for the endocytosis of hemoglobin and hemoglobin/haptoglobin complexes and is nearly exclusively expressed on monocytes and macrophages. CD163 is induced by IL-10 and glucocorticoids while proinflammatory cytokines like TNF reduce its expression. The cytokine IL-6 which exerts pro- and anti-inflammatory effects depending on the signaling pathway activated strongly upregulates CD163. Anti-inflammatory cells involved in the down-modulation of inflammation express high CD163 which controls immune response. Ligands of the toll-like receptors 2, 4 and 5 stimulate ectodomain shedding of CD163 thereby releasing soluble CD163 (sCD163) which mediates cellular uptake of free hemoglobin. Soluble CD163 circulates in blood and is increased in serum of critically ill patients, in chronic inflammatory and infectious diseases. Serum concentrations of sCD163 are related to disease severity and are suitable biomarkers for diagnosis, prognosis and therapeutic drug monitoring in several inflammatory disorders. Raised sCD163 even predicts comorbidity and mortality in some diseases. Relationship of CD163/sCD163 and disease severity demonstrates a fundamental role of monocytes/macrophages in various diseases. CD163 is a target to specifically deliver drugs to macrophages intending advanced therapeutic efficiency and minimization of adverse reactions. In this review article factors regulating CD163 expression and shedding, current knowledge on the function of CD163 and sCD163, and inflammatory diseases where CD163 and/or sCD163 are mostly increased are summarized.

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