从染色体损伤到触发多种免疫反应的辐照后果

Sherien Abdelwhab Montaser
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摘要

本研究旨在通过细胞分裂阻断微核(cytokinetics -block micronuclear, CBMN)试验研究辐照后的DNA损伤及其相应的免疫反应。测定干扰素- α、β用于先天性反应,干扰素-γ用于获得性反应,TNF- α和免疫球蛋白浓度IgG和IgM。6份人体血液样本分为4组(对照组和3组辐照组),暴露剂量分别为0.5 - 2 Gy和4 Gy。三胞胎血样(对照组和辐照组)在辐照1小时后培养72小时。γ -辐照在所有实验剂量(0.5 -2.0和4.0 Gy)下均诱导IFN-α(先天免疫标志)显著增加。在4.0 Gy剂量下,IFN-β也显著增加。结果显示,在2.0和4.0 Gy时,代表获得性免疫反应的IFN-γ显著增加。IgG和IgM水平的升高证实了这一结果。TNF-α晚期免疫反应在2.0和4.0 Gy时开始显著增加。1.0 Gy和4Gy组TNF-α和IFN-β与对照组相比有显著差异,4Gy组与1.0 Gy组相比有显著升高。与对照组和其他剂量相比,所有剂量的INF-α均显著增加。与对照组相比,1.0和4.0 Gy时IFN-γ显著增加,但两者之间无显著差异。我们得出结论,免疫系统可以感知细胞受损。来自各种来源(如辐照)的Mni可导致类似于病毒感染期间观察到的免疫反应。
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Irradiation Consequences from Chromosome Damages to Triggering of Diverse Immunological Responses
Present work was designed to investigate DNA damages post irradiation via cytokinesis-block micronucleus (CBMN) test and its corresponding immunological response. Determination of interferon- α, β for innate, interferon-γ for acquired response, TNF- α and immunoglobulin concentration IgG & IgM. Six human blood samples were divided into 4 groups (control & 3irradiated) which exposed to doses (0.5 - 2 and 4 Gy). Triplet blood samples (control and irradiated groups) were cultured for 72 hours after 1 hour of irradiation. γ - Irradiation induced significant increase of IFN-α (innate immunology hallmark) in all experimental doses (0.5 -2.0 and 4.0 Gy). IFN-β also recorded significant increase with control at dose 4.0 Gy. The results showed significant increase in IFN-γ representing acquired immune response at 2.0 and 4.0 Gy. These results confirmed by exhibits increase in the level of IgG and IgM production. TNF-α late immune response started to give significant increase at 2.0 and 4.0 Gy. TNF-α and IFN-β recorded significant difference when compared with control at 1.0 and 4Gy exposure also 4Gy group recorded significant increase compared with 1.0 Gy exposure. INF-α recorded significant increase at all doses when compared with control and each other. IFN-γ recorded significant increase in 1.0 and 4.0 Gy when compared with control with no significant difference between them. We conclude that immune system can sense when cells damaged. Mni which come from a variety of sources such as irradiation can lead to an immune response similar to that observed during viral infection.
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