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In vitro Quality of Platelets with Low Plasma Carryover Treated with Ultraviolet C Light for Pathogen Inactivation.经紫外线C光处理以实现病原体灭活的低血浆残留血小板的体外质量
Transfus Med Hemother. 2016 May;43(3):190-7. doi: 10.1159/000441830. Epub 2015 Nov 5.
2
The impact of refrigerated storage of UVC pathogen inactivated platelet concentrates on in vitro platelet quality parameters.紫外线C病原体灭活血小板浓缩物冷藏储存对体外血小板质量参数的影响。
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3
Effect of increased agitation speed on pathogen inactivation efficacy and in vitro quality in UVC-treated platelet concentrates.增加搅拌速度对紫外线C处理的血小板浓缩物中病原体灭活效果和体外质量的影响。
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Characteristics of the THERAFLEX UV-Platelets pathogen inactivation system - an update.THERAFLEX紫外线血小板病原体灭活系统的特点——最新进展
Transfus Apher Sci. 2012 Apr;46(2):221-9. doi: 10.1016/j.transci.2012.01.008. Epub 2012 Feb 24.
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In vitro effects on platelets irradiated with short-wave ultraviolet light without any additional photoactive reagent using the THERAFLEX UV-Platelets method.采用 THERAFLEX UV-Platelets 方法,在没有任何其他光活性试剂的情况下,用短波紫外线照射血小板的体外效应。
Vox Sang. 2011 Jul;101(1):35-43. doi: 10.1111/j.1423-0410.2010.01454.x. Epub 2010 Dec 22.
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Cryopreservation of UVC pathogen-inactivated platelets.UVC 病原体失活血小板的冷冻保存。
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Inactivation of SARS-CoV-2 infectivity in platelet concentrates or plasma following treatment with ultraviolet C light or with methylene blue combined with visible light.经紫外线 C 光或亚甲蓝联合可见光处理后,血小板浓缩物或血浆中的 SARS-CoV-2 感染性失活。
Transfusion. 2023 Feb;63(2):288-293. doi: 10.1111/trf.17238. Epub 2023 Jan 8.
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In vitro function of platelets treated with ultraviolet C light for pathogen inactivation: a comparative study with nonirradiated and gamma-irradiated platelets.经紫外线C光处理以实现病原体灭活的血小板的体外功能:与未辐照和γ辐照血小板的对比研究
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Reduction of Zika virus infectivity in platelet concentrates after treatment with ultraviolet C light and in plasma after treatment with methylene blue and visible light.用紫外线C光处理后血小板浓缩物中寨卡病毒感染性的降低以及用亚甲蓝和可见光处理后血浆中寨卡病毒感染性的降低。
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Inactivation of three emerging viruses - severe acute respiratory syndrome coronavirus, Crimean-Congo haemorrhagic fever virus and Nipah virus - in platelet concentrates by ultraviolet C light and in plasma by methylene blue plus visible light.经紫外线 C 照射灭活血小板浓缩液中的三种新兴病毒 - 严重急性呼吸综合征冠状病毒、克里米亚-刚果出血热病毒和尼帕病毒 - 以及经亚甲基蓝联合可见光灭活血浆中的上述三种病毒。
Vox Sang. 2020 Apr;115(3):146-151. doi: 10.1111/vox.12888. Epub 2020 Jan 12.

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Impact of different pathogen reduction technologies on the biochemistry, function, and clinical effectiveness of platelet concentrates: An updated view during a pandemic.不同病原体减少技术对血小板浓缩物的生化、功能和临床效果的影响:大流行期间的最新观点。
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UV light-emitting diode (UV-LED) at 265 nm as a potential light source for disinfecting human platelet concentrates.265nm 的紫外线发光二极管 (UV-LED) 作为一种潜在的光源,可用于消毒人血小板浓缩物。
PLoS One. 2021 May 20;16(5):e0251650. doi: 10.1371/journal.pone.0251650. eCollection 2021.
4
Platelet Pathogen Reduction Technologies Alter the MicroRNA Profile of Platelet-Derived Microparticles.血小板病原体灭活技术改变了血小板衍生微粒的微小RNA谱。
Front Cardiovasc Med. 2020 Mar 19;7:31. doi: 10.3389/fcvm.2020.00031. eCollection 2020.
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Platelet spreading on fibrinogen matrix, a reliable and sensitive marker of platelet functional activity during storage.血小板在纤维蛋白原基质上的铺展,是储存期间血小板功能活性的可靠和敏感的标志物。
J Thromb Thrombolysis. 2019 Oct;48(3):430-438. doi: 10.1007/s11239-019-01916-8.
6
Ultraviolet-Based Pathogen Inactivation Systems: Untangling the Molecular Targets Activated in Platelets.基于紫外线的病原体灭活系统:解析血小板中被激活的分子靶点
Front Med (Lausanne). 2018 May 7;5:129. doi: 10.3389/fmed.2018.00129. eCollection 2018.
7
Could Microparticles Be the Universal Quality Indicator for Platelet Viability and Function?微粒能否成为血小板活力和功能的通用质量指标?
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本文引用的文献

1
Ultraviolet C light pathogen inactivation treatment of platelet concentrates preserves integrin activation but affects thrombus formation kinetics on collagen in vitro.血小板浓缩物的紫外线C光病原体灭活处理可保留整合素激活,但会影响体外胶原蛋白上的血栓形成动力学。
Transfusion. 2015 Oct;55(10):2404-14. doi: 10.1111/trf.13137. Epub 2015 Apr 25.
2
Tolerance of platelet concentrates treated with UVC-light only for pathogen reduction--a phase I clinical trial.仅用于病原体灭活的经紫外线C光处理的血小板浓缩物的耐受性——一项I期临床试验。
Vox Sang. 2015 Jul;109(1):44-51. doi: 10.1111/vox.12247. Epub 2015 Mar 6.
3
In vitro function of platelets treated with ultraviolet C light for pathogen inactivation: a comparative study with nonirradiated and gamma-irradiated platelets.经紫外线C光处理以实现病原体灭活的血小板的体外功能:与未辐照和γ辐照血小板的对比研究
Transfusion. 2015 Jun;55(6):1169-77. doi: 10.1111/trf.12963. Epub 2014 Dec 18.
4
Pathogen inactivation technologies for cellular blood components: an update.细胞血液成分的病原体灭活技术:更新。
Transfus Med Hemother. 2014 Jul;41(4):309-25. doi: 10.1159/000365646. Epub 2014 Jul 21.
5
Analysis of leucocyte antibodies, cytokines, lysophospholipids and cell microparticles in blood components implicated in post-transfusion reactions with dyspnoea.对与输血后呼吸困难反应相关的血液成分中的白细胞抗体、细胞因子、溶血磷脂和细胞微粒进行分析。
Vox Sang. 2015 Jan;108(1):27-36. doi: 10.1111/vox.12190. Epub 2014 Aug 18.
6
Pathogen reduction by ultraviolet C light effectively inactivates human white blood cells in platelet products.通过紫外线C光进行病原体灭活可有效使血小板制品中的人白细胞失活。
Transfusion. 2015 Feb;55(2):337-47. doi: 10.1111/trf.12836. Epub 2014 Aug 19.
7
The efficacy of the ultraviolet C pathogen inactivation system in the reduction of Babesia divergens in pooled buffy coat platelets.紫外线 C 病原体灭活系统在减少汇集缓冲血小板中的巴贝虫 divergens 的效果。
Transfusion. 2014 Sep;54(9):2207-16. doi: 10.1111/trf.12598. Epub 2014 Mar 25.
8
The hemostatic activity of cryopreserved platelets is mediated by phosphatidylserine-expressing platelets and platelet microparticles.冷冻保存血小板的止血活性由表达磷脂酰丝氨酸的血小板和血小板微粒介导。
Transfusion. 2014 Aug;54(8):1917-26. doi: 10.1111/trf.12578. Epub 2014 Feb 17.
9
In vitro and in vivo characterization of ultraviolet light C-irradiated human platelets in a 2 event mouse model of transfusion.在输血 2 次事件小鼠模型中,对经紫外线 C 照射的人血小板进行体外和体内特性分析。
PLoS One. 2013 Nov 1;8(11):e79869. doi: 10.1371/journal.pone.0079869. eCollection 2013.
10
In vitro assessment of buffy-coat derived platelet components suspended in SSP+ treated with the INTERCEPT Blood system.使用INTERCEPT血液系统处理的悬浮于SSP+中的血沉棕黄层衍生血小板成分的体外评估。
Transfus Med. 2013 Apr;23(2):121-9. doi: 10.1111/tme.12020. Epub 2013 Mar 11.

经紫外线C光处理以实现病原体灭活的低血浆残留血小板的体外质量

In vitro Quality of Platelets with Low Plasma Carryover Treated with Ultraviolet C Light for Pathogen Inactivation.

作者信息

Johnson Lacey, Hyland Ryan, Tan Shereen, Tolksdorf Frank, Sumian Chryslain, Seltsam Axel, Marks Denese

机构信息

Research and Development, Australian Red Cross Blood Service, Sydney, NSW, Australia.

MacoPharma International GmbH, Langen, Germany.

出版信息

Transfus Med Hemother. 2016 May;43(3):190-7. doi: 10.1159/000441830. Epub 2015 Nov 5.

DOI:10.1159/000441830
PMID:27403091
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4924470/
Abstract

BACKGROUND

The THERAFLEX UV-Platelets system uses shortwave ultraviolet C light (UVC, 254 nm) to inactivate pathogens in platelet components. Plasma carryover influences pathogen inactivation and platelet quality following treatment. The plasma carryover in the standard platelets produced by our institution are below the intended specification (<30%).

METHODS

A pool and split study was carried out comparing untreated and UVC-treated platelets with <30% plasma carryover (n = 10 pairs). This data was compared to components that met specifications (>30% plasma). The platelets were tested over storage for in vitro quality.

RESULTS

Platelet metabolism was accelerated following UVC treatment, as demonstrated by increased glucose consumption and lactate production. UVC treatment caused increased externalization of phosphatidylserine on platelets and microparticles, activation of the GPIIb/IIIa receptor (PAC-1 binding), and reduced hypotonic shock response. Platelet function, as measured with thrombelastogram, was not affected by UVC treatment. Components with <30% plasma were similar to those meeting specification with the exception of enhanced glycolytic metabolism.

CONCLUSION

This in vitro analysis demonstrates that treatment of platelets with <30% plasma carryover with the THERAFLEX UV-Platelets system affects some aspects of platelet metabolism and activation, although in vitro platelet function was not negatively impacted. This study also provides evidence that the treatment specifications of plasma carryover could be extended to below 30%.

摘要

背景

THERAFLEX紫外线血小板系统使用短波紫外线C光(UVC,254纳米)来灭活血小板成分中的病原体。血浆残留会影响病原体灭活效果以及处理后血小板的质量。我们机构生产的标准血小板中的血浆残留低于预期规格(<30%)。

方法

进行了一项混合与拆分研究,比较血浆残留<30%的未处理和经紫外线C处理的血小板(n = 10对)。将该数据与符合规格(血浆>30%)的成分进行比较。对血小板在储存期间进行体外质量测试。

结果

紫外线C处理后血小板代谢加速,表现为葡萄糖消耗增加和乳酸生成增加。紫外线C处理导致血小板和微粒上磷脂酰丝氨酸的外化增加、糖蛋白IIb/IIIa受体激活(PAC-1结合)以及低渗休克反应降低。用血栓弹力图测量的血小板功能不受紫外线C处理的影响。血浆<30%的成分与符合规格的成分相似,只是糖酵解代谢增强。

结论

这项体外分析表明,使用THERAFLEX紫外线血小板系统处理血浆残留<30%的血小板会影响血小板代谢和激活的某些方面,尽管体外血小板功能未受到负面影响。本研究还提供了证据,表明血浆残留的处理规格可以扩展至低于30%。