Viability of Plasmodium falciparum parasites in human plasma under different storage conditions.

IF 1.8 4区 医学 Q3 HEMATOLOGY Vox Sanguinis Pub Date : 2024-12-11 DOI:10.1111/vox.13781
Anna Lavrentieva, Miranda S Oakley, Clifford T H Hayashi, Victoria F Majam, Anne F Eder, Carlos H Villa, Sanjai Kumar
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Abstract

Background and objectives: Malaria risk deferral policies are important for mitigating the risk of transfusion-transmitted malaria and apply to all transfusable components, including plasma. While donors of plasma components are deferred for malaria risk in the United States, the viability of intraerythrocytic Plasmodium falciparum parasites present in human plasma components stored under different temperatures and durations has not been previously reported.

Materials and methods: We spiked human plasma with a low level of ring-stage P. falciparum-infected red blood cells and then determined their viability in cultures after storage at room temperature (22°C), refrigeration (4°C) and frozen conditions at -20 and -80°C.

Results: P. falciparum parasites spiked in human plasma remained viable after storage at 22°C for a maximum of 7 days. When stored at 4°C, parasites were viable after 1 and 3 days of storage and only for 1 day after storage at -20°C. Storage at -80°C had a cryopreserving effect and parasites remained viable for up to 176 days, the longest period tested.

Conclusion: P. falciparum parasites can survive for short durations in human plasma when stored at room temperature, or in refrigerated or frozen conditions at -20°C. However, when stored at -80°C, viable parasites were detected for up to 176 days, the maximum duration for which viability was assessed. In summary, Plasmodium parasites can survive in human plasma under different storage conditions and pose a risk of transfusion-transmitted infection.

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不同贮存条件下恶性疟原虫在人血浆中的生存能力。
背景和目标:疟疾风险延迟政策对于减轻输血传播疟疾的风险非常重要,并适用于包括血浆在内的所有可输注成分。虽然在美国,血浆组分的供体因疟疾风险而被推迟,但在不同温度和持续时间下储存的人血浆组分中存在的红细胞内恶性疟原虫寄生虫的生存能力以前没有报道。材料和方法:我们在人血浆中加入低水平的环期恶性疟原虫感染的红细胞,然后在室温(22°C)、冷藏(4°C)和-20和-80°C冷冻条件下测定其在培养物中的生存能力。结果:人血浆中的恶性疟原虫在22℃下保存最多7天后仍能存活。在4°C条件下,寄生物在1天和3天后都有活力,在-20°C条件下寄生物在1天后才有活力。在-80°C的低温保存条件下,寄生虫可以存活176天,这是实验中最长的时间。结论:恶性疟原虫在室温、-20℃冷藏或冷冻条件下可在人血浆中存活较短时间。然而,当储存在-80°C时,可检测到活寄生虫长达176天,这是评估活力的最长持续时间。总之,疟原虫可以在不同的储存条件下在人血浆中存活,并具有输血传播感染的风险。
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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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