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移植前交叉配型阳性而供者特异性抗人类白细胞抗原抗体阴性的原因:单中心经验。

Causes of Positive Pretransplant Crossmatches in the Absence of Donor-Specific Anti-Human Leukocyte Antigen Antibodies: A Single-Center Experience.

机构信息

Department of Laboratory Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.

出版信息

Ann Lab Med. 2021 Jul 1;41(4):429-435. doi: 10.3343/alm.2021.41.4.429.

DOI:10.3343/alm.2021.41.4.429
PMID:33536364
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7884190/
Abstract

Pretransplant crossmatch (XM) testing is widely used for detecting preformed donor-specific antibodies (DSAs) against human leukocyte antigen (HLA). However, in some cases, there is a positive XM result in the absence of HLA-DSAs, the cause of which was rarely identified. We reviewed the causes of sequential positive XM results at a single center and analyzed the presence of non-HLA antibodies in patients with an unexplained positive pretransplant XM result. Among 251 patients with T-cell/B-cell complement-dependent cytotoxicity (CDC) or flow cytometric crossmatch (FCXM) positivity, HLA-DSAs were confirmed in 88 (35.1%) by a single antigen bead (SAB) assay, 150 (59.8%) used rituximab (anti-CD20), and 13 (5.2%) had neither HLA-DSAs nor a desensitization history. Anti-angiotensin II type 1 receptor IgG and 33 non-HLA antibodies were tested in the 13 patients with an unexplained positive pretransplant XM result, and more than one non-HLA antibody were revealed in all these patients; 11 patients had non-HLA antibodies reported to be associated with graft rejection, and two patients experienced rejection episode after kidney transplantation. Our study suggests considering non-HLA antibodies testing when a CDC or FCXM test is positive without a definite cause. Assessing non-HLA antibodies might be useful for interpreting XM results and evaluating immunologic risk in transplant recipients.

摘要

移植前交叉配型(XM)检测广泛用于检测针对人类白细胞抗原(HLA)的预先形成的供体特异性抗体(DSA)。然而,在某些情况下,即使不存在 HLA-DSA,也会出现 XM 阳性结果,其原因很少被确定。我们回顾了单一中心连续 XM 阳性结果的原因,并分析了移植前 XM 阳性结果原因不明的患者中是否存在非 HLA 抗体。在 251 例 T 细胞/B 细胞补体依赖性细胞毒性(CDC)或流式细胞交叉配型(FCXM)阳性的患者中,通过单抗原珠(SAB)检测在 88 例(35.1%)中确认了 HLA-DSA,150 例(59.8%)使用利妥昔单抗(抗-CD20),13 例(5.2%)既没有 HLA-DSA 也没有脱敏史。在 13 例移植前 XM 阳性结果原因不明的患者中检测了抗血管紧张素 II 型 1 受体 IgG 和 33 种非 HLA 抗体,所有这些患者均显示出一种以上的非 HLA 抗体;11 例患者的非 HLA 抗体与移植物排斥反应有关,2 例患者在肾移植后发生排斥反应。我们的研究表明,当 CDC 或 FCXM 检测阳性且无明确原因时,应考虑进行非 HLA 抗体检测。评估非 HLA 抗体可能有助于解释 XM 结果并评估移植受者的免疫风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4407/7884190/20269b457720/alm-41-4-429-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4407/7884190/20269b457720/alm-41-4-429-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4407/7884190/20269b457720/alm-41-4-429-f1.jpg

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