南非输血患者中乙型肝炎病毒、人类 T 淋巴细胞病毒和人体免疫缺陷病毒的流行情况

IF 1.8 4区 医学 Q3 HEMATOLOGY
Vox Sanguinis Pub Date : 2024-09-11 DOI:10.1111/vox.13735
Reynier J. Willemse, Christa J. Grobler, Edward L. Murphy, Nareg Roubinian, Charl Colemen, Solly Machaba, Marion Vermeulen
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引用次数: 0

摘要

背景和目标南非的人类免疫缺陷病毒(HIV)和乙型肝炎病毒(HBV)感染率很高,人类 T 淋巴细胞病毒(HTLV)感染率较低。这些病原体都具有输血传播性(TT),但决定是否实施预防性筛查取决于对输血患者背景流行率的了解。我们测定了南非医院输血者中 HIV、HBV 和 HTLV I/II 的流行情况。材料与方法我们在南非国家血液服务机构 (SANBS) 服务的 634 家南非医院获得了用于血液交叉配血的身份非连接样本。ABBOTT Alinity S® 免疫化学发光系统检测了 HIV、HBV 和 HTLV I/II 抗体。使用罗氏 Cobas® 8000 对重复反应样本进行确认。结果 HIV、HBV 和 HTLV 的总感染率分别为 37.8%、7.4% 和 0.6%。受血者中的艾滋病毒感染率是普通人群估计值的两倍。与私立医院患者相比,公立医院患者的艾滋病毒和乙肝病毒感染率明显较高。女性的 HIV 感染率明显更高,而男性的 HBV 感染率明显更高(不包括未知性别结果)。可测量的 HTLV 感染率表明这种感染在南非流行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The prevalence of hepatitis B virus, human T‐lymphotropic virus and human immunodeficiency virus in patients receiving blood transfusions in South Africa
Background and ObjectivesSouth Africa has a high prevalence of human immunodeficiency virus (HIV) and hepatitis B virus (HBV) and to a lesser extent human T‐lymphotropic virus (HTLV). Each of these agents is transfusion‐transmissible (TT) but deciding whether to implement preventive screening depends upon knowledge of background prevalence in transfused patients. We determined the prevalence of HIV, HBV and HTLV I/II among blood transfusion recipients in South African hospitals.Materials and MethodsWe obtained identity‐unlinked samples used for blood cross‐matching at 634 South African hospitals served by the South African National Blood Service (SANBS). The ABBOTT Alinity S® Immunochemiluminescent system measured HIV, HBV and HTLV I/II antibodies. Repeatedly reactive samples were confirmed using the Roche Cobas® 8000. Logistic regression was performed to investigate the determinants of associations for HIV, HBV and HTLV infections.ResultsThe overall prevalences of HIV, HBV and HTLV were 37.8%, 7.4% and 0.6%, respectively. The HIV prevalence in blood recipients was twice as high as general population estimates. Public hospital patients had a significantly higher prevalence compared with private hospital patients for HIV and HBV. HIV prevalence was significantly higher in females, and HBV prevalence was significantly higher in males, excluding the unknown gender results.ConclusionPatients receiving blood transfusions in South Africa have high rates of HIV and HBV infection that should be taken into consideration when determining donor screening strategies for other viral infections. Measurable prevalence of HTLV indicates endemicity of this infection in South Africa.
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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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