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登革病毒诱导骨髓抑制的机制。

Mechanisms of dengue virus-induced bone marrow suppression.

作者信息

La Russa V F, Innis B L

机构信息

Department of Hematology and Vascular Biology, Walter Reed Army Institute of Research, Washington, DC 20307-5100, USA.

出版信息

Baillieres Clin Haematol. 1995 Mar;8(1):249-70. doi: 10.1016/s0950-3536(05)80240-9.

Abstract

Infection with many flaviviruses is associated with transient suppression of haematopoiesis. Of the flaviviruses of man, none are more accessible to clinical and laboratory study than dengue. Consequently, the clinical syndrome of dengue-associated bone marrow suppression has been well documented. A review of experimental dengue infections of volunteers and histopathological studies of bone marrow from patients with severe dengue virus infection suggests that marrow suppression evolves rapidly through several phases: (1) onset of marrow suppression within 3-4 days of infection; (2) onset of host inflammatory responses in the marrow and of fever shortly thereafter; (3) occurrence of a neutrophil nadir on the fourth to fifth day after onset of fever; (4) almost simultaneously, immune activation sufficient to neutralize viraemia and accelerate elimination of infected cells; (5) remission of symptoms; and (6) resolution of cytopenias. Clinical observations and experimental data bear on possible mechanisms of dengue virus-mediated marrow suppression. Work from the authors' laboratory in which long-term bone marrow cultures were used to investigate interactions between dengue virus and bone marrow cells (stromal elements and haematopoietic progenitors) is also reviewed. Long-term marrow culture (LTMC) was a useful experimental system. In vitro, early blast cells as well as the more differentiated haematopoietic elements were abortively infected, killed and eliminated by phagocytosis by specialized marrow macrophages called dendritic cells. Moreover, the ARC from stroma rather than haematopoietic precursors were productively infected. When ARC were infected, stroma failed to support haematopoiesis. Cytokine production by virus-infected stromal cells was altered. A hypothesis is proposed to account for dengue virus-induced marrow suppression. Down-regulation of haematopoiesis is probably a protective mechanism of the microenvironment that limits injury to the marrow stem/progenitor cell compartment during the subsequent process of elimination of infected cells.

摘要

感染多种黄病毒与造血功能的短暂抑制有关。在人类黄病毒中,没有哪种病毒比登革热病毒更便于进行临床和实验室研究。因此,登革热相关骨髓抑制的临床综合征已有充分记录。对志愿者的实验性登革热感染以及重症登革热病毒感染患者骨髓的组织病理学研究进行回顾后发现,骨髓抑制会迅速经历几个阶段:(1)感染后3 - 4天内出现骨髓抑制;(2)骨髓中宿主炎症反应开始,随后不久出现发热;(3)发热开始后第4至5天出现中性粒细胞最低点;(4)几乎同时,免疫激活足以中和病毒血症并加速清除受感染细胞;(5)症状缓解;(6)血细胞减少症消退。临床观察和实验数据有助于了解登革热病毒介导的骨髓抑制的可能机制。本文还回顾了作者实验室的工作,该工作利用长期骨髓培养来研究登革热病毒与骨髓细胞(基质成分和造血祖细胞)之间的相互作用。长期骨髓培养(LTMC)是一个有用的实验系统。在体外,早期母细胞以及分化程度更高的造血成分被一种称为树突状细胞的特殊骨髓巨噬细胞吞噬而发生流产性感染、死亡并被清除。此外,来自基质而非造血前体的ARC被有效感染。当ARC被感染时,基质无法支持造血。病毒感染的基质细胞的细胞因子产生发生改变。本文提出了一个假说来解释登革热病毒诱导的骨髓抑制。造血功能的下调可能是一种微环境的保护机制,在随后清除受感染细胞的过程中限制对骨髓干/祖细胞区室的损伤。

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