Prospective Cohort Study to Assess the Effect of Storage Duration, Leuko-Filtration, and Gamma Irradiation on Cell-Free DNA in Red Cell Components.

IF 1.9
Nitesh Gupta, Dheeraj Khetan, Rajendra Chaudhary, Jai Shankar Shukla
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引用次数: 3

Abstract

Introduction: Damage to a cell and the loss of integrity of its cell membrane leads to the release of endogenous immunogenic molecules, which together are classified as "damage-associated molecular patterns" (DAMPs). Cell-free DNA (cf-DNA) released from nucleosomes may serve as a proco-agulant cofactor and may be an important mediator of immunomodulatory and proinflammatory effects associated with blood transfusion.

Objectives: To assess the levels of cf-DNA in supernatants of stored red cell components and the effect of leukoreduction and gamma irradiation on the release of cf-DNA during storage.

Methods: This is a prospective cohort study on 99 stored red cell components, randomly divided into three groups - buffy coat (BC)-depleted, leuko-filtered (LP), and irradiated (IR) packed red blood cells. Red cell supernatants were drawn over a period of 21 days at three different time points (day 0, 7, and 21) from the study units. cf-DNA extraction was done and quantified by a bench top fluorometer. Change in cf-DNA content, rate of change (μg/day), and percent change were estimated and compared across different groups.

Results: cf-DNA content increased (p = 0.000) with storage duration in the BC (median = 238.66 μg, interquartile range [IQR] = 168.42 on day 21 vs. median = 9.44 μg, IQR = 5.23 on day 0) and IR groups (p = 0.000) (median = 245.55 μg, IQR = 253.88 on day 21 vs. median = 7.07 μg, IQR = 13.58 on day 0), while there was a decreasing trend (p = 0.032) in the LP group (median = 4.55 μg, IQR = 10.73 on day 21 vs. median = 8.66 μg, IQR = 6.56 on day 0). The median rate of change in cf-DNA content (11.13 μg/day) and percent change in cf-DNA content (median = 4,106.16%) was highest in the IR group.

Conclusions: Stored red cell components contain significant amount of cf-DNA. Release of cf-DNA is further aggravated by irradiation while leukoreduction leads to a decrease in cf-DNA content.

评估储存时间、白细胞过滤和γ辐射对红细胞成分中游离DNA影响的前瞻性队列研究。
对细胞的损伤和细胞膜完整性的丧失导致内源性免疫原性分子的释放,它们一起被归类为“损伤相关分子模式”(DAMPs)。核小体释放的无细胞DNA (cf-DNA)可能作为一种促凝辅助因子,可能是与输血相关的免疫调节和促炎作用的重要介质。目的:评价储存红细胞成分上清液中cf-DNA的水平,以及白细胞还原和γ辐射对储存过程中cf-DNA释放的影响。方法:这是一项对99种储存红细胞成分的前瞻性队列研究,随机分为三组-淡色被(BC)耗尽,白细胞过滤(LP)和辐照(IR)填充红细胞。在21天的时间里,在三个不同的时间点(第0、7和21天)从研究单位中抽取红细胞上清液。用台式荧光仪进行cf-DNA提取和定量。估计并比较不同组间cf-DNA含量、变化率(μg/day)和百分比的变化。结果:cf-DNA内容增加(p = 0.000)的存储时间公元前(值= 238.66μg,四分位范围(差)= 168.42天21日与中值= 9.44μg,差0天= 5.23)和IR组(p = 0.000)(值= 245.55μg,差= 253.88天21日与中值= 7.07μg,差0天= 13.58),同时有降低的趋势(p = 0.032) LP组(值= 4.55μg,差= 10.73天21日与中值= 8.66μg,IQR = 6.56,第0天)。IR组cf-DNA含量的中位数变化率(11.13 μg/d)和百分比变化率(中位数= 4,106.16%)最高。结论:储存的红细胞成分含有大量的cf-DNA。辐照进一步加剧了cf-DNA的释放,而白细胞减少导致cf-DNA含量下降。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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