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本文引用的文献

1
Improved flow cytometry based cytotoxicity and binding assay for clinical antibody HLA crossmatching.用于临床抗体HLA交叉配型的基于流式细胞术的改进细胞毒性和结合测定法。
Hum Immunol. 2015 Nov;76(11):849-57. doi: 10.1016/j.humimm.2015.09.047. Epub 2015 Sep 30.
2
A review of rituximab, the first anti-CD20 monoclonal antibody used in the treatment of B non-Hodgkin's lymphomas.利妥昔单抗综述,首个用于治疗B细胞非霍奇金淋巴瘤的抗CD20单克隆抗体。
Future Oncol. 2015;11(9):1327-42. doi: 10.2217/fon.15.57.
3
Interference of therapeutic antibodies used in desensitization protocols on lymphocytotoxicity crossmatch results.脱敏方案中使用的治疗性抗体对淋巴细胞毒性交叉配型结果的干扰。
Transpl Immunol. 2015 Jun;32(3):151-5. doi: 10.1016/j.trim.2015.04.004. Epub 2015 Apr 30.
4
Deciphering complement interference in anti-human leukocyte antigen antibody detection with flow beads assays.解析流式微球检测抗人白细胞抗原抗体时补体干扰。
Transplantation. 2014 Sep 27;98(6):625-31. doi: 10.1097/TP.0000000000000315.
5
Artificially Positive Crossmatches Not Leading to the Refusal of Kidney Donations due to the Usage of Adequate Diagnostic Tools.由于使用了适当的诊断工具,人为阳性交叉配型未导致肾脏捐赠被拒绝。
Case Rep Transplant. 2013;2013:746395. doi: 10.1155/2013/746395. Epub 2013 Mar 28.
6
Correlation between Luminex donor-specific crossmatches and levels of donor-specific antibodies in pretransplantation screening.移植前筛查中Luminex供者特异性交叉配型与供者特异性抗体水平之间的相关性
Tissue Antigens. 2013 Jul;82(1):16-20. doi: 10.1111/tan.12128. Epub 2013 Apr 29.
7
New crossmatch technique eliminates interference by humanized and chimeric monoclonal antibodies.新的交叉配型技术消除了人源化和嵌合单克隆抗体的干扰。
Transplant Proc. 2005 Mar;37(2):640-2. doi: 10.1016/j.transproceed.2004.12.066.
8
Pronase treatment facilitates alloantibody flow cytometric and cytotoxic crossmatching in the presence of rituximab.链霉蛋白酶处理有助于在利妥昔单抗存在的情况下进行同种抗体流式细胞术和细胞毒性交叉配型。
Hum Immunol. 2004 Aug;65(8):803-9. doi: 10.1016/j.humimm.2004.06.001.

肾供体先前接受利妥昔单抗治疗后出现的B细胞交叉配型假阳性。

False Positive B-Cells Crossmatch after Prior Rituximab Exposure of the Kidney Donor.

作者信息

Desoutter Judith, Apithy Marie-Joëlle, Bartczak Ségolène, Guillaume Nicolas

机构信息

Department of Histocompatibility, Amiens University Medical Center, 80000 Amiens, France.

出版信息

Case Rep Transplant. 2016;2016:4534898. doi: 10.1155/2016/4534898. Epub 2016 Apr 28.

DOI:10.1155/2016/4534898
PMID:27239362
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4864553/
Abstract

Crossmatching is essential prior to kidney transplantation to confirm compatibility between the donor and the recipient, particularly to prevent acute antibody-mediated rejection. An unexpected positive crossmatch may be obtained in recipients with an autoimmune disease or preexisting antibodies not detected by single-antigen bead array due to complement interference or who have been previously treated by desensitization protocols such as rituximab, antithymocyte globulin, or intravenous immunoglobulins. We report donor and recipient investigations that revealed unexpected positive B-cells crossmatch, probably due to donor cells, as the donor had received rituximab therapy shortly before organ harvesting, in a context of severe idiopathic thrombocytopenic purpura. We consequently detected unexpected Class II IgG complement-dependent cytotoxicity for all sera tested. Other laboratory investigations failed to elucidate the reasons for this recipient-related positivity.

摘要

在肾移植前进行交叉配型至关重要,以确认供体和受体之间的相容性,特别是为了预防急性抗体介导的排斥反应。在患有自身免疫性疾病的受体中,或由于补体干扰,通过单抗原珠阵列未检测到预先存在的抗体的受体中,或之前接受过诸如利妥昔单抗、抗胸腺细胞球蛋白或静脉注射免疫球蛋白等脱敏方案治疗的受体中,可能会获得意外的阳性交叉配型结果。我们报告了供体和受体的调查情况,结果显示出现了意外的B细胞阳性交叉配型,可能是由于供体细胞导致的,因为在严重特发性血小板减少性紫癜的情况下,供体在器官获取前不久接受了利妥昔单抗治疗。因此,我们检测到所有测试血清中出现了意外的II类IgG补体依赖性细胞毒性。其他实验室检查未能阐明这种与受体相关的阳性结果的原因。