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用巨噬细胞集落刺激因子(CSF-1)治疗小鼠可预防由小鼠α、β和γ干扰素诱导的体内骨髓抑制。

Treatment of mice with macrophage colony stimulating factor (CSF-1) prevents the in vivo myelosuppression induced by murine alpha, beta, and gamma interferons.

作者信息

Koren S, Klimpel G R, Fleischmann W R

出版信息

J Biol Response Mod. 1986 Oct;5(5):481-9.

PMID:3095498
Abstract

Interferon (IFN) treatment has been shown to suppress the bone marrow in mice and humans, causing a leukopenia. In vitro studies with the mouse system have shown that colony stimulating factors (CSFs) antagonize the bone marrow suppressive, but not the antiviral or antiproliferative activities of IFNs. Partially purified murine macrophage colony stimulating factor (CSF-1) was evaluated for its ability to antagonize the myelosuppressive effect of murine (Mu) IFNs in vivo. All three interferon types (MuIFN-alpha, MuIFN-beta, and MuIFN-gamma) were used. IFNs and CSF-1 were administered subcutaneously for 3 successive days, blood was drawn by retro-ocular bleeding, and myelo-suppression was quantitated by subjecting the blood to total white blood cell (WBC) counts and to differential counts. The IFNs had similar effects, though MuIFN-gamma was a significantly more potent (50- to 100-fold) myelosuppressive agent than MuIFN-alpha or MuIFN-beta. Treatment with each of the three IFNs caused a reduction in the total WBC count (up to 40% reduction) and a generalized reduction of each of the three major leukocytes (lymphocytes, segmented polymorphonuclear leukocytes, and monocytes). Treatment with CSF-1 did not affect the total WBC count, but did cause a shift in the relative ratios of the leukocytes, decreasing the relative percentage of lymphocytes, and increasing the relative percentage of segmented polymorphonuclear leukocytes and monocytes. Combined treatment with CSF-1 and IFN inhibited the myelosuppressive activity of the IFNs, and restored the total WBC count to control levels. This restoration was largely due to increased levels of segmented polymorphonuclear leukocytes and monocytes.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

干扰素(IFN)治疗已被证明会抑制小鼠和人类的骨髓,导致白细胞减少。对小鼠系统的体外研究表明,集落刺激因子(CSF)可拮抗骨髓抑制作用,但不能拮抗IFN的抗病毒或抗增殖活性。评估了部分纯化的小鼠巨噬细胞集落刺激因子(CSF-1)在体内拮抗小鼠(Mu)IFN骨髓抑制作用的能力。使用了所有三种类型的干扰素(MuIFN-α、MuIFN-β和MuIFN-γ)。IFN和CSF-1连续3天皮下给药,通过眼后静脉丛取血,并通过对血液进行白细胞(WBC)总数计数和分类计数来定量骨髓抑制。尽管MuIFN-γ作为骨髓抑制剂比MuIFN-α或MuIFN-β的效力显著更强(50至100倍),但这三种IFN具有相似的作用。用这三种IFN中的每一种进行治疗都会导致白细胞总数减少(最多减少40%),并且三种主要白细胞(淋巴细胞、分叶多形核白细胞和单核细胞)均普遍减少。用CSF-1治疗不影响白细胞总数,但确实导致白细胞相对比例发生变化,降低淋巴细胞的相对百分比,并增加分叶多形核白细胞和单核细胞的相对百分比。CSF-1与IFN联合治疗可抑制IFN的骨髓抑制活性,并使白细胞总数恢复到对照水平。这种恢复主要是由于分叶多形核白细胞和单核细胞水平的增加。(摘要截断于250字)

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