Dose-dependent inactivation of Plasmodium falciparum in red blood cell concentrates by treatment with short-wavelength ultraviolet light.

IF 1.8 4区 医学 Q3 HEMATOLOGY Vox Sanguinis Pub Date : 2024-10-01 Epub Date: 2024-07-24 DOI:10.1111/vox.13714
Swantje Fischer, Susann Zilkenat, Mona Rosse, Torsten J Schulze, Axel Seltsam, Wiebke Handke, Bernd Lepenies, Ute Gravemann
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Abstract

Background and objectives: Plasmodium species are naturally transmitted by Anopheles mosquitos. The parasite infects red blood cells (RBCs) and can be transfused with blood products. In non-endemic areas, the main risk of infection arises from travellers coming back and people immigrating from malaria-endemic regions. Endemic countries face a permanent risk of infection from transfusion-transmitted malaria (TTM). TTM may cause life-threatening complications in patients dependent on blood donations. This study aimed to investigate the efficacy of Plasmodium falciparum inactivation in RBC units by treatment with short-wavelength ultraviolet C (UVC) light in the absence of photochemical additives.

Materials and methods: RBC units were spiked with P. falciparum to a parasite density of 0.1%-1% and irradiated with up to 4.5 J/cm2 UVC. The parasite density of UVC-treated dilution series and untreated controls were compared over 3 weeks after irradiation.

Results: The lowest dose of 1.5 J/cm2 UVC led to a 3.1 log reduction in parasite load compared with the untreated control. The inactivation capacity was dose-dependent. Strikingly, 4.5 J/cm2 led to ≥5.3 log unit reduction, which was equivalent to a complete inactivation in two out of three experiments.

Conclusion: Pathogen reduction with UVC light was previously shown to be effective for different bacteria and viruses, but the inactivation of parasites in RBC concentrates was not addressed until now. The present study provides evidence for significant inactivation of P. falciparum-infected RBCs by UVC light.

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用短波紫外线处理红细胞浓缩液中的恶性疟原虫的剂量依赖性灭活。
背景和目标:疟原虫由按蚊自然传播。寄生虫会感染红细胞(RBC),并可通过输血产品传播。在非疟疾流行地区,主要的感染风险来自从疟疾流行地区回来的旅行者和移民。疟疾流行国家长期面临着输血传播疟疾(TTM)的感染风险。输血传播疟疾可能会给依赖献血的患者带来危及生命的并发症。本研究旨在探讨在不使用光化学添加剂的情况下,用短波紫外线 C(UVC)处理红细胞单位灭活恶性疟原虫的效果:将恶性疟原虫添加到寄生虫密度为 0.1%-1% 的红细胞中,并用高达 4.5 J/cm2 的紫外线照射。在照射后的 3 周内,比较了经紫外线处理的稀释系列和未经处理的对照组的寄生虫密度:结果:与未处理的对照组相比,最低剂量为 1.5 J/cm2 的紫外线可使寄生虫数量减少 3.1 log。灭活能力与剂量有关。引人注目的是,4.5 焦耳/平方厘米的紫外线可使寄生虫数量减少≥5.3 个对数单位,这相当于三个实验中有两个实验完全灭活了寄生虫:结论:以前的研究表明,紫外线能有效减少不同细菌和病毒的病原体,但直到现在才解决了浓缩红细胞中寄生虫的灭活问题。本研究提供了紫外线能显著灭活恶性疟原虫感染的红细胞的证据。
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来源期刊
Vox Sanguinis
Vox Sanguinis 医学-血液学
CiteScore
4.40
自引率
11.10%
发文量
156
审稿时长
6-12 weeks
期刊介绍: Vox Sanguinis reports on important, novel developments in transfusion medicine. Original papers, reviews and international fora are published on all aspects of blood transfusion and tissue transplantation, comprising five main sections: 1) Transfusion - Transmitted Disease and its Prevention: Identification and epidemiology of infectious agents transmissible by blood; Bacterial contamination of blood components; Donor recruitment and selection methods; Pathogen inactivation. 2) Blood Component Collection and Production: Blood collection methods and devices (including apheresis); Plasma fractionation techniques and plasma derivatives; Preparation of labile blood components; Inventory management; Hematopoietic progenitor cell collection and storage; Collection and storage of tissues; Quality management and good manufacturing practice; Automation and information technology. 3) Transfusion Medicine and New Therapies: Transfusion thresholds and audits; Haemovigilance; Clinical trials regarding appropriate haemotherapy; Non-infectious adverse affects of transfusion; Therapeutic apheresis; Support of transplant patients; Gene therapy and immunotherapy. 4) Immunohaematology and Immunogenetics: Autoimmunity in haematology; Alloimmunity of blood; Pre-transfusion testing; Immunodiagnostics; Immunobiology; Complement in immunohaematology; Blood typing reagents; Genetic markers of blood cells and serum proteins: polymorphisms and function; Genetic markers and disease; Parentage testing and forensic immunohaematology. 5) Cellular Therapy: Cell-based therapies; Stem cell sources; Stem cell processing and storage; Stem cell products; Stem cell plasticity; Regenerative medicine with cells; Cellular immunotherapy; Molecular therapy; Gene therapy.
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