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白细胞介素-1治疗对亚致死剂量辐射后造血及免疫系统重建的影响。

The influence of IL-1 treatment on the reconstitution of the hemopoietic and immune systems after sublethal radiation.

作者信息

Morrissey P, Charrier K, Bressler L, Alpert A

机构信息

Immunex Corporation, Seattle, WA 98101.

出版信息

J Immunol. 1988 Jun 15;140(12):4204-10.

PMID:3286769
Abstract

The influence of IL-1 administration on the recovery of the hemopoietic and immune systems from sublethal irradiation was assessed. Mice were irradiated (750 R) and injected twice daily with purified recombinant derived IL-1 beta (200 ng/injection). At various times after irradiation, the functional capacity of the hemopoietic and immune systems was determined. It was found that IL-1 therapy resulted in a significantly greater number of granulocyte-macrophage-CSF responsive colony-forming cells in the bone marrow of the irradiated mice on days 5 and 11 postirradiation but not at later times. In addition the radiation induced neutropenia recovered quicker in the IL-1-treated mice with significantly greater numbers of peripheral blood granulocytes being seen on days 15 and 20 after irradiation. The influence of IL-1 therapy on the recovery of the immune system was also assessed. Of note was the observation that mice receiving IL-1 therapy had chronically hypoplastic thymi. Although thymic cellularity increased with time after irradiation in the control mice, there was no such increase in the IL-1-treated mice. Similarly, the number of pre-B cells in the marrow of these mice was also diminished. Thus, in the IL-1-treated mice the regeneration of the peripheral immune function was retarded, characterized by a general lymphopenia and decreased splenic responses to mitogenic stimuli.

摘要

评估了白细胞介素-1(IL-1)给药对亚致死剂量辐射后造血和免疫系统恢复的影响。对小鼠进行辐射(750伦琴),并每天两次注射纯化的重组IL-1β(每次注射200纳克)。在辐射后的不同时间,测定造血和免疫系统的功能能力。结果发现,IL-1治疗使受辐射小鼠骨髓中粒细胞-巨噬细胞集落刺激因子反应性集落形成细胞的数量在辐射后第5天和第11天显著增加,但在之后的时间没有增加。此外,在接受IL-1治疗的小鼠中,辐射诱导的中性粒细胞减少恢复得更快,在辐射后第15天和第20天,外周血粒细胞数量显著增加。还评估了IL-1治疗对免疫系统恢复的影响。值得注意的是,接受IL-1治疗的小鼠胸腺长期发育不全。虽然对照小鼠辐射后胸腺细胞数量随时间增加,但接受IL-1治疗的小鼠没有这种增加。同样,这些小鼠骨髓中前B细胞的数量也减少。因此,在接受IL-1治疗的小鼠中,外周免疫功能的再生受到阻碍,其特征是普遍淋巴细胞减少和脾脏对有丝分裂原刺激的反应降低。

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