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使用同种异体反应性T细胞检测法鉴别同种异体移植中的抗供体反应

Discrimination of Anti-Donor Response in Allogeneic Transplantation Using an Alloreactive T-Cell Detection Assay.

作者信息

Arata Ryosuke, Tanimine Naoki, Seidakhmetov Akhmet, Ide Kentaro, Tanaka Yuka, Ohdan Hideki

机构信息

Department of Gastroenterological and Transplant Surgery, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.

出版信息

Transpl Int. 2025 Jan 28;38:13879. doi: 10.3389/ti.2025.13879. eCollection 2025.

DOI:10.3389/ti.2025.13879
PMID:39936124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11810569/
Abstract

Understanding donor-reactive T-cell behavior post-transplantation is challenging owing to the rarity and diversity of these cells. Here, we aimed to evaluate the relevance of an assay for rapidly detecting alloreactive T cells in a mouse transplantation model. After 18 h of one-way mixed lymphocyte reaction (MLR) culture with pre-activated donor-derived stimulators, CD4 and CD8 donor-reactive T cells were identified by CD154 and CD137 expression, respectively. Using full MHC mismatched mouse skin transplant models, we observed an increased donor-reactive T-cell proportion by direct presentation with elevated interferon gamma and granzyme B production 7 days post-transplantation, before graft rejection. Immunosuppression with CTLA-4 IgG and anti-CD154 antibody varied depending on donor-recipient strain combinations. On day 7, donor-reactive CD8 T-cell proportions were lower in the tolerance model (BALB/c to C3H/HeJ) than in the rejection model (BALB/c to C57BL/6); conventional proliferation readout after 4 days of MLR could not distinguish these responses. Overall, although the conventional readout for evaluating T-cell proliferation following an MLR quantifies the precursor frequency of alloreactive T cells, the assay reported herein assesses T-cell activation markers after a short-term MLR to characterize immediate immune status. These findings offer a promising tool to elucidate immune responses post-transplantation.

摘要

由于供体反应性T细胞的稀有性和多样性,了解其移植后的行为具有挑战性。在此,我们旨在评估一种检测方法在小鼠移植模型中快速检测同种异体反应性T细胞的相关性。在用预激活的供体来源刺激物进行单向混合淋巴细胞反应(MLR)培养18小时后,分别通过CD154和CD137表达鉴定CD4和CD8供体反应性T细胞。使用完全主要组织相容性复合体(MHC)不匹配的小鼠皮肤移植模型,我们观察到在移植后7天、移植物排斥反应之前,通过直接呈递,供体反应性T细胞比例增加,同时干扰素γ和颗粒酶B的产生也增加。使用CTLA-4 IgG和抗CD154抗体进行免疫抑制因供体-受体品系组合而异。在第7天,耐受模型(BALB/c到C3H/HeJ)中的供体反应性CD8 T细胞比例低于排斥模型(BALB/c到C57BL/6);MLR 4天后的传统增殖读数无法区分这些反应。总体而言,虽然用于评估MLR后T细胞增殖的传统读数可量化同种异体反应性T细胞的前体频率,但本文报道的检测方法在短期MLR后评估T细胞激活标志物,以表征即时免疫状态。这些发现为阐明移植后的免疫反应提供了一个有前景的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6ff/11810569/c7c88a1e5bee/ti-38-13879-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6ff/11810569/0c5ef83663d9/TI_ti-2025-13879_wc_abs.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6ff/11810569/0c5ef83663d9/TI_ti-2025-13879_wc_abs.jpg
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Activation and regulation of alloreactive T cell immunity in solid organ transplantation.实体器官移植中同种异体反应性 T 细胞免疫的激活和调节。
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