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慢性病贫血

The anemia of chronic disease.

作者信息

Lee G R

出版信息

Semin Hematol. 1983 Apr;20(2):61-80.

PMID:6348957
Abstract

The anemia of chronic disease (ACD) is defined as a mild anemia associated with a chronic inflammatory, infectious or neoplastic illness and with a characteristic disturbance of iron metabolism. Many of the findings in ACD can be accounted for by release of a monokine called leukocyte endogenous mediator (LEM), endogenous pyrogen, or interleukin-1. This substance is released from "activated" monocytes. Bacterial endotoxins, certain lymphokines and phagocytic challenges are among the factors stimulating its biosynthesis. LEM induces fever, leukocytosis, biosynthesis. LEM induces fever, leukocytosis, and a variety of biochemical changes, including hypoferremia and alterations in plasma protein synthesis, collectively known as the "acute phase response." It is proposed that ACD results from the long-term elaboration of LEM and that release of this material is the common pathogenetic factor found in the illnesses that are associated with ACD. Some suggestions are made for testing the hypothesis. The hypoferremia associated with ACD is probably caused by defective release of iron from cells--particularly from macrophages, but also from hepatocytes and intestinal epithelium. Two possible mechanisms for this abnormality have been proposed: liberation of lactoferrin from neutrophilic leukocytes and induction of apoferritin synthesis. Neither mechanism has been established. Erythrokinetic studies in ACD have detected a modest reduction of erythrocyte survival without an adequate compensatory increase in the rate of red cell production. The reduced erythrocyte survival is probably related to an increase in phagocytic activity by activated macrophages. Impaired bone marrow response is partly related to the restricted iron supply, but there is substantial evidence for an additional defect in erythropoietin secretion. In some malignant diseases, there is evidence of an additional abnormality: impaired marrow response to a normal amount of erythropoietin. The nature of the erythropoietic defects and the relation of LEM to them remain to be established.

摘要

慢性病贫血(ACD)被定义为一种与慢性炎症、感染或肿瘤性疾病相关的轻度贫血,伴有铁代谢的特征性紊乱。ACD的许多表现可由一种称为白细胞内源性介质(LEM)、内源性致热原或白细胞介素-1的单核因子释放来解释。这种物质从“活化的”单核细胞释放。细菌内毒素、某些淋巴因子和吞噬刺激是刺激其生物合成的因素。LEM可引起发热、白细胞增多以及多种生化变化,包括低铁血症和血浆蛋白合成改变,这些变化统称为“急性期反应”。有人提出,ACD是LEM长期产生的结果,这种物质的释放是与ACD相关疾病中常见的致病因素。文中提出了一些检验该假说的建议。与ACD相关的低铁血症可能是由于细胞(特别是巨噬细胞,但也包括肝细胞和肠上皮细胞)中铁释放缺陷所致。针对这种异常情况提出了两种可能的机制:从中性粒细胞释放乳铁蛋白和诱导脱铁铁蛋白合成。但这两种机制均未得到证实。对ACD的红细胞动力学研究发现,红细胞存活时间略有缩短,而红细胞生成率没有相应的充分代偿性增加。红细胞存活时间缩短可能与活化巨噬细胞吞噬活性增加有关。骨髓反应受损部分与铁供应受限有关,但有大量证据表明促红细胞生成素分泌存在额外缺陷。在一些恶性疾病中,有证据表明存在另一种异常:骨髓对正常量促红细胞生成素的反应受损。红细胞生成缺陷的本质以及LEM与它们的关系仍有待确定。

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