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本文引用的文献

1
Rejection of intestinal allotransplants is driven by memory T helper type 17 immunity and responds to infliximab.肠道同种异体移植的排斥反应是由记忆 T 辅助型 17 免疫驱动的,并对英夫利昔单抗有反应。
Am J Transplant. 2021 Mar;21(3):1238-1254. doi: 10.1111/ajt.16283. Epub 2020 Sep 25.
2
PD-1 CD8 resident memory T cells balance immunity and fibrotic sequelae.PD-1+CD8 记忆性 T 细胞平衡免疫与纤维化后遗症。
Sci Immunol. 2019 Jun 14;4(36). doi: 10.1126/sciimmunol.aaw1217.
3
Inflammatory Cytokine Networks in Gastrointestinal Tract Graft vs. Host Disease.胃肠道移植物抗宿主病中的炎症细胞因子网络。
Front Immunol. 2019 Feb 22;10:163. doi: 10.3389/fimmu.2019.00163. eCollection 2019.
4
Long-term survival in visceral transplant recipients in the new era: A single-center experience.新时代内脏移植受者的长期生存:单中心经验。
Am J Transplant. 2019 Jul;19(7):2077-2091. doi: 10.1111/ajt.15269. Epub 2019 Mar 26.
5
Circulating HLA-DR+CD4+ effector memory T cells resistant to CCR5 and PD-L1 mediated suppression compromise regulatory T cell function in tuberculosis.循环 HLA-DR+CD4+效应记忆 T 细胞对 CCR5 和 PD-L1 介导的抑制具有抗性,从而损害结核分枝杆菌中调节性 T 细胞的功能。
PLoS Pathog. 2018 Sep 19;14(9):e1007289. doi: 10.1371/journal.ppat.1007289. eCollection 2018 Sep.
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PD-1+CD8+ T cells are clonally expanding effectors in human chronic inflammation.PD-1+CD8+ T 细胞在人类慢性炎症中呈克隆性扩增效应器。
J Clin Invest. 2018 Oct 1;128(10):4669-4681. doi: 10.1172/JCI96107. Epub 2018 Aug 2.
7
Risk Factors for Severe Acute Graft-versus-Host Disease in Donor Graft Composition.供者移植物成分中重症急性移植物抗宿主病的危险因素。
Biol Blood Marrow Transplant. 2018 Mar;24(3):467-477. doi: 10.1016/j.bbmt.2017.11.026. Epub 2017 Nov 29.
8
Acute Graft-versus-Host Disease - Biologic Process, Prevention, and Therapy.急性移植物抗宿主病——生物学过程、预防与治疗
N Engl J Med. 2017 Nov 30;377(22):2167-2179. doi: 10.1056/NEJMra1609337.
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IL-7 receptor heterogeneity as a mechanism for repertoire change during postdepletional homeostatic proliferation and its relation to costimulation blockade-resistant rejection.IL-7 受体异质性作为耗竭后稳态增殖过程中库变化的机制及其与共刺激阻断耐药排斥反应的关系。
Am J Transplant. 2018 Mar;18(3):720-730. doi: 10.1111/ajt.14589. Epub 2017 Dec 12.
10
Tissue-Resident Lymphocytes in Solid Organ Transplantation: Innocent Passengers or the Key to Organ Transplant Survival?实体器官移植中的组织驻留淋巴细胞:无辜的过客还是器官移植存活的关键?
Transplantation. 2018 Mar;102(3):378-386. doi: 10.1097/TP.0000000000002001.

CD69+ 驻留记忆 T 细胞与肠道移植中的移植物抗宿主病有关。

CD69+ resident memory T cells are associated with graft-versus-host disease in intestinal transplantation.

机构信息

MedStar Georgetown Transplant Institute, MedStar Georgetown University Hospital and the Center for Translational Transplant Medicine, Georgetown University Medical Center, Washington, District of Columbia.

Department of Pathology, MedStar Georgetown University Hospital, Washington, District of Columbia.

出版信息

Am J Transplant. 2021 May;21(5):1878-1892. doi: 10.1111/ajt.16405. Epub 2021 Feb 17.

DOI:10.1111/ajt.16405
PMID:33226726
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10364625/
Abstract

Graft-versus-host disease (GvHD) is a common, morbid complication after intestinal transplantation (ITx) with poorly understood pathophysiology. Resident memory T cells (T ) are a recently described CD69+ memory T cell subset localizing to peripheral tissue. We observed that T effector memory cells (T ) in the blood increase during GvHD and hypothesized that they derive from donor graft CD69+T migrating into host blood and tissue. To probe this hypothesis, graft and blood lymphocytes from 10 ITx patients with overt GvHD and 34 without were longitudinally analyzed using flow cytometry. As hypothesized, CD4+ and CD8+CD69+T were significantly increased in blood and grafts of GvHD patients, alongside higher cytokine and activation marker expression. The majority of CD69+T were donor derived as determined by multiplex immunostaining. Notably, CD8/PD-1 was significantly elevated in blood prior to transplantation in patients who later had GvHD, and percentages of HLA-DR, CD57, PD-1, and naïve T cells differed significantly between GvHD patients who died vs. those who survived. Overall, we demonstrate that (1) there were significant increases in T at the time of GvHD, possibly of donor derivation; (2) donor T in the graft are a possible source; and (3) potential biomarkers for the development and prognosis of GvHD exist.

摘要

移植物抗宿主病(GvHD)是肠移植(ITx)后的一种常见且严重的并发症,其发病机制尚不清楚。驻留记忆 T 细胞(T 细胞)是最近描述的一种 CD69+记忆 T 细胞亚群,定位于外周组织。我们观察到,GvHD 期间血液中的效应记忆 T 细胞(T 细胞)增加,并假设它们来源于移植物中 CD69+T 细胞向宿主血液和组织的迁移。为了验证这一假设,我们对 10 例有明显 GvHD 的 ITx 患者和 34 例无 GvHD 的患者的移植物和血液淋巴细胞进行了纵向分析,使用流式细胞术。正如假设的那样,GvHD 患者的血液和移植物中 CD4+和 CD8+CD69+T 细胞明显增加,同时细胞因子和激活标志物的表达也更高。通过多重免疫染色确定,大多数 CD69+T 细胞来源于供体。值得注意的是,在发生 GvHD 的患者中,在移植前血液中 CD8/PD-1 明显升高,且 HLA-DR、CD57、PD-1 和幼稚 T 细胞的比例在死亡和存活的 GvHD 患者之间有显著差异。总体而言,我们证明了(1)在 GvHD 发生时 T 细胞数量显著增加,可能来源于供体;(2)移植物中的供体 T 细胞可能是其来源;(3)存在用于 GvHD 发展和预后的潜在生物标志物。