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随机输血单位中移植前供体HLA - DR抗原暴露与供体抗原特异性低反应性的发展

Pretransplant exposure to donor HLA-DR antigen in random transfusion units and the development of donor antigen-specific hyporeactivity.

作者信息

Jackson A, McSherry C, Butters K, Diko M, Almond P S, Matas A J, Reinsmoen N L

机构信息

Department of Surgery, University of Minnesota, Minneapolis 55455, USA.

出版信息

Hum Immunol. 1997 Jul;55(2):148-53. doi: 10.1016/s0198-8859(97)00098-0.

DOI:10.1016/s0198-8859(97)00098-0
PMID:9361966
Abstract

Our previous studies have shown that the in vitro assay of donor antigen-specific hyporeactivity is a useful marker for identifying solid organ transplant recipients (kidney, lung and heart) at low risk for immunologic complications (i.e., late acute rejection episodes and chronic rejection). Donor antigen-specific hyporeactivity is defined as a significantly decreased post- vs. pretransplant proliferative response to donor antigens while response to third-party controls remains unchanged. We analyzed whether exposure to the same HLA-DR antigen pretransplant via random blood transfusion and posttransplant via the transplanted organ influenced the development of hyporeactivity. Thirty previously nontransfused recipients, each receiving two 150 ml pretransplant random blood transfusions, were assessed for hyporeactivity at 1 year posttransplant. Of the 12 recipients with pretransplant exposure to kidney HLA-DR via transfusions, 6 (50%) developed hyporesponsiveness; in contrast, of the 18 recipients who were not preexposed, only 3 (15%) exhibited this form of immunomodulation. Of interest, 2 of the 3 hyporesponsive recipients who were not preexposed, received units containing HLA-DR antigens previously shown to share crossreactive epitopes with the kidney HLA-DR. In conclusion, these results suggest a increased incidence in the development of hyporeactivity in patients receiving pretransplant transfusions which share an HLA-DR antigen with the transplanted kidney.

摘要

我们之前的研究表明,供体抗原特异性低反应性的体外检测是一种有用的标志物,可用于识别实体器官移植受者(肾、肺和心脏)发生免疫并发症(即晚期急性排斥反应和慢性排斥反应)的低风险情况。供体抗原特异性低反应性定义为移植后与移植前对供体抗原的增殖反应显著降低,而对第三方对照的反应保持不变。我们分析了移植前通过随机输血以及移植后通过移植器官接触相同的HLA - DR抗原是否会影响低反应性的发生。30名之前未输血的受者,每人在移植前接受两次150毫升随机输血,在移植后1年评估其低反应性。在12名移植前通过输血接触肾HLA - DR的受者中,6名(50%)出现低反应性;相比之下,在18名未预先接触的受者中,只有3名(15%)表现出这种免疫调节形式。有趣的是,3名未预先接触的低反应性受者中有2名接受了含有先前显示与肾HLA - DR共享交叉反应表位的HLA - DR抗原的血制品。总之,这些结果表明,移植前输血且所输血液制品与移植肾共享HLA - DR抗原的患者,低反应性的发生率增加。

相似文献

1
Pretransplant exposure to donor HLA-DR antigen in random transfusion units and the development of donor antigen-specific hyporeactivity.随机输血单位中移植前供体HLA - DR抗原暴露与供体抗原特异性低反应性的发展
Hum Immunol. 1997 Jul;55(2):148-53. doi: 10.1016/s0198-8859(97)00098-0.
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Evidence that improved late renal transplant outcome correlates with the development of in vitro donor antigen-specific hyporeactivity.改善肾移植后期结果与体外供体抗原特异性低反应性的发展相关的证据。
Transplantation. 1993 May;55(5):1017-23. doi: 10.1097/00007890-199305000-00013.
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Allogeneic microchimerism and donor antigen-specific hyporeactivity in lung transplant recipients.肺移植受者中的同种异体微嵌合体和供体抗原特异性低反应性
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Improved long-term graft outcome in lung transplant recipients who have donor antigen-specific hyporeactivity.在具有供体抗原特异性低反应性的肺移植受者中,长期移植结果得到改善。
J Heart Lung Transplant. 1994 Jan-Feb;13(1 Pt 1):30-6; discussion 36-7.
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HLA-DR matched transfusions: development of donor-specific T- and B-cell antibodies and renal allograft outcome.HLA-DR匹配输血:供体特异性T细胞和B细胞抗体的产生及肾移植结局
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Organ-specific patterns of donor antigen-specific hyporeactivity and peripheral blood allogeneic microchimerism in lung, kidney, and liver transplant recipients.肺、肾和肝移植受者中供体抗原特异性低反应性及外周血同种异体微嵌合体的器官特异性模式。
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Effect of one-HLA-DR-antigen-matched and completely HLA-DR-mismatched blood transfusions on survival of heart and kidney allografts.单HLA - DR抗原匹配及完全HLA - DR不匹配输血对心脏和肾脏同种异体移植物存活的影响。
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An apparent paradoxical effect of pretransplant blood transfusions. Its association with decreased anti-HLA antibody formation following unsuccessful renal transplantation.
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A new in vitro approach to determine acquired tolerance in long-term kidney allograft recipients.一种用于确定长期肾移植受者获得性耐受的新体外方法。
Transplantation. 1990 Nov;50(5):783-90. doi: 10.1097/00007890-199011000-00009.

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