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首页> 外文期刊>European journal of immunogenetics: official journal of the British Society for Histocompatibility and Immunogenetics >Presence of HLA antibodies in single-donor-derived fresh frozen plasma compared with pooled, solvent detergent-treated plasma (Octaplas(R)).
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Presence of HLA antibodies in single-donor-derived fresh frozen plasma compared with pooled, solvent detergent-treated plasma (Octaplas(R)).

机译:与汇集的,溶剂去污剂处理的血浆(Octaplas)相比,在单供体来源的新鲜冷冻血浆中存在HLA抗体。

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摘要

Summary Adverse reactions to plasma transfusion are well documented. One of the most serious hazards of transfusion, transfusion-related acute lung injury (TRALI), has nearly as high an incidence of mortality and major morbidity as that reported for the transfusion of incorrect blood components. The specific mechanisms of plasma component-induced adverse reactions remain unclear, but a major contribution may be related to the presence of alloantibodies. In this study, a laboratory analysis was undertaken to determine the presence of HLA antibodies in leucodepleted single-donor-derived fresh frozen plasma (FFP). A comparison was made with a pooled plasma product that has undergone solvent detergent treatment. In total, 58 plasma samples from single-donor units of leucodepleted FFP were tested along with samples from 12 units (three for each ABO blood group) of the pooled plasma (Octaplas((R)); Octapharma Ltd, Coventry, UK), for the presence of HLA antibodies. HLA-specific enzyme-linked immunosorbent assay (ELISA) methods were used to screen for their presence, and complement-dependent cytotoxicity and flow cytometry analyses were used to further define their presence, specificity and class [immunoglobulin G (IgG)/IgM]. In the study groups, HLA antibodies were found to be present in five of the single-donor units (9%) while the pooled plasma samples tested negative.
机译:小结对血浆输注的不良反应已有详细记录。输血相关的急性肺损伤(TRALI)是最严重的输血危险之一,其死亡率和主要发病率的发生率与输血不正确的血液成分的发生率几乎相同。血浆成分引起的不良反应的具体机制仍不清楚,但是主要的作用可能与同种抗体的存在有关。在这项研究中,进行了实验室分析,以确定亮白单单供体来源的新鲜冰冻血浆(FFP)中是否存在HLA抗体。与经过溶剂去污剂处理的合并血浆产品进行了比较。总共测试了58个来自全白血球完整FFP单供体单位的血浆样品,以及来自合并血浆的12个单位(每个ABO血型为3个)的样品(Octaplas®; Octapharma Ltd,英国考文垂), HLA抗体的存在。 HLA特异性酶联免疫吸附测定(ELISA)方法用于筛选其存在,补体依赖性细胞毒性和流式细胞仪分析用于进一步定义其存在,特异性和类别[免疫球蛋白G(IgG)/ IgM]。在研究组中,发现五种单供体单位(9%)中存在HLA抗体,而合并血浆样本测试为阴性。

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