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有共同子女的夫妻间肾移植的结局:单中心应用T细胞清除诱导治疗的经验及文献综述

Outcome of Husband-to-Wife Kidney Transplantation With Mutual Children: Single Center Experience Using T Cell-Depleting Induction and Review of the Literature.

作者信息

Senn Lisa, Wehmeier Caroline, Hönger Gideon, Geiger Irene, Amico Patrizia, Hirt-Minkowski Patricia, Steiger Jürg, Dickenmann Michael, Schaub Stefan

机构信息

Clinic for Transplantation Immunology and Nephrology, University Hospital Basel, Basel, Switzerland.

HLA-Diagnostics and Immungenetics, Department of Laboratory Medicine, University Hospital Basel, Basel, Switzerland.

出版信息

Front Med (Lausanne). 2021 Aug 2;8:724851. doi: 10.3389/fmed.2021.724851. eCollection 2021.

DOI:10.3389/fmed.2021.724851
PMID:34409057
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8365247/
Abstract

Few data on husband-to-wife transplantations with mutual children (H2W) exist in the current era. We investigated the outcome of H2W transplantations ( = 25) treated with T cell-depleting induction compared to women with prior pregnancies also receiving their first HLA-mismatched kidney transplant, but from a different donor source: (i) other living donor ( = 52) and (ii) deceased donor ( = 120). Seventy-four percent of the women had ≥2 pregnancies; median follow-up time was 5 years. Death-censored allograft survival was significantly lower in the H2W group compared to the other two groups ( = 0.03). Three of four graft losses in the H2W group were due to rejection. 5-year patient survival in the H2W group was high and similar compared to the other living donor group (100 vs. 98%; = 0.28). The incidence of (sub)clinical antibody-mediated rejection was higher in the H2W group (36 vs. 20 vs. 18%) ( = 0.10). The frequency of infections was similar among the three groups. No immunological parameter was predictive for rejection or graft loss in H2W transplantations. In conclusion, H2W transplantation is a valuable option, but associated with a higher risk for allograft loss due to rejection despite T cell-depleting induction. Further research is required for better risk prediction on an individual patient level.

摘要

在当今时代,关于有共同子女的夫妻间肾移植(夫供妻肾移植)的数据很少。我们研究了接受去除T细胞诱导治疗的25例夫供妻肾移植患者的结局,并与既往有过妊娠且首次接受HLA配型不相合肾移植的女性进行比较,但后者的供体来源不同:(i)其他活体供体(52例)和(ii) deceased donor(120例)。74%的女性有≥2次妊娠;中位随访时间为5年。与其他两组相比,夫供妻肾移植组的死亡删失移植物存活率显著较低(P = 0.03)。夫供妻肾移植组的4例移植物丢失中有3例是由于排斥反应。夫供妻肾移植组的5年患者存活率较高,与其他活体供体组相似(100%对98%;P = 0.28)。夫供妻肾移植组(亚)临床抗体介导排斥反应的发生率较高(36%对20%对18%)(P = 0.10)。三组间感染频率相似。在夫供妻肾移植中,没有免疫参数可预测排斥反应或移植物丢失。总之,夫供妻肾移植是一种有价值的选择,但尽管进行了去除T细胞诱导治疗,仍与因排斥反应导致移植物丢失的较高风险相关。需要进一步研究以在个体患者水平上进行更好的风险预测。 (注:“deceased donor”未明确准确中文表述,暂保留英文)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8365247/51ee04bc03fe/fmed-08-724851-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8365247/de382dc3ab10/fmed-08-724851-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8365247/51ee04bc03fe/fmed-08-724851-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8365247/de382dc3ab10/fmed-08-724851-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8365247/51ee04bc03fe/fmed-08-724851-g0002.jpg

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Outcome of Husband-to-Wife Kidney Transplantation With Mutual Children: Single Center Experience Using T Cell-Depleting Induction and Review of the Literature.有共同子女的夫妻间肾移植的结局:单中心应用T细胞清除诱导治疗的经验及文献综述
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本文引用的文献

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Ann Transplant. 2020 Nov 6;25:e925229. doi: 10.12659/AOT.925229.
2
Development of an immunogenicity score for HLA-DQ eplets: A conceptual study.开发 HLA-DQ 表位免疫原性评分:概念研究。
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3
Toward defining the immunogenicity of HLA epitopes: Impact of HLA class I eplets on antibody formation during pregnancy.
迈向定义HLA表位的免疫原性:HLA I类表位对孕期抗体形成的影响。
HLA. 2020 Nov;96(5):589-600. doi: 10.1111/tan.14054. Epub 2020 Sep 10.
4
HLA-specific memory B-cell detection in kidney transplantation: Insights and future challenges.肾移植中 HLA 特异性记忆 B 细胞的检测:研究进展与未来挑战。
Int J Immunogenet. 2020 Jun;47(3):227-234. doi: 10.1111/iji.12493. Epub 2020 May 10.
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Clinical importance of extended second field high-resolution HLA genotyping for kidney transplantation.扩大的第二领域高分辨率HLA基因分型在肾移植中的临床重要性。
Am J Transplant. 2020 Dec;20(12):3367-3378. doi: 10.1111/ajt.15938. Epub 2020 May 15.
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