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VIRTUAL CROSSMATCH DETERMINES DONOR-RECIPIENT PAIRS FOR HEART TRANSPLANTATION

机译:虚拟交叉迁移决定了心脏移植的供体接受者对

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Introduction: Solid phase immunoassays allow identification of unacceptable HLA antigens for the prediction of compatible donor/recipient pairs. This process is referred to as virtual crossmatch (vXM). Since 2001, we have used solid phase immunoassays to define the specificity of HLA antibodies for our sensitized patients on the kidney, heart, or lung transplant waitlists and utilized the vXM to select donors for heart, lung transplantations. The aim of the study was to evaluate the accuracy of the vXM used for donor selection for sensitized heart recipients. Patients and Methods: Patients who received heart transplants between January 2005 and September 2009 were included in this study. Sensitization was defined by presence of positive flow PRA and defined specificity of HLA antibodies. Solid phase immunoassays were used to screen for HLA antibodies and define unacceptable HLA antigens for each sensitized patient. Utilizing the principle of vXM, only donors without unacceptable HLA antigens were used for non-emergent sensitized patients. For sensitized patients needing emergent transplant, anti-HLA antibodies not detected at a dilution of 1:16 were considered low titer and were not considered for donor selection. All XMs were performed by flow cytometry since middle of 2005.
机译:介绍:固相免疫测定允许鉴定不可接受的HLA抗原以预测兼容的供体/受体对。此过程称为虚拟交叉频率(VxM)。自2001年以来,我们使用了固相免疫测定,以定义肾脏,心脏或肺移植等候患者的敏化患者的HLA抗体的特异性,并利用VxM选择心脏肺移植的供体。该研究的目的是评估用于助长心脏受体的捐助者选择的VXM的准确性。患者及方法:在本研究中纳入2005年1月至2009年9月期间的心脏移植患者。敏化由存在的阳性流量PRA和定义的HLA抗体特异性定义。固相免疫测定用于筛选HLA抗体,并针对每个敏化患者定义不可接受的HLA抗原。利用VXM的原理,仅使用没有不可接受的HLA抗原的供体用于非新兴致敏患者。对于需要出苗移植的敏化患者,在稀释1:16下未检测到的抗HLA抗体被认为是低滴度,并且不考虑供体选择。自2005年中期以来,通过流式细胞仪进行所有XMS。

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