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异基因干细胞移植治疗急性淋巴细胞白血病后 EBV 相关移植后 B 细胞淋巴增殖性疾病:免疫抑制减少后的肿瘤消退——一例报告。

EBV-associated post-transplantation B-cell lymphoproliferative disorder following allogenic stem cell transplantation for acute lymphoblastic leukaemia: tumor regression after reduction of immunosuppression--a case report.

机构信息

Institute of Pathology, University of Leipzig, Liebigstrasse 26, Leipzig, Germany.

出版信息

Diagn Pathol. 2010 Mar 31;5:21. doi: 10.1186/1746-1596-5-21.

DOI:10.1186/1746-1596-5-21
PMID:20356360
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2853499/
Abstract

Epstein-Barr virus (EBV)-associated B-cell post-transplantation lymphoproliferative disorder (PTLD) is a severe complication following stem cell transplantation. This is believed to occur as a result of iatrogenic immunosuppression leading to a relaxation of T-cell control of EBV infection and thus allowing viral reactivation and proliferation of EBV-infected B-lymphocytes. In support of this notion, reduction of immunosuppressive therapy may lead to regression of PTLD.We present a case of an 18-year-old male developing a monomorphic B-cell PTLD 2 months after receiving an allogenic stem cell transplant for acute lymphoblastic leukemia. Reduction of immunosuppressive therapy led to regression of lymphadenopathy. Nevertheless, the patient died 3 months afterwards due to extensive graft-vs.-host-disease and sepsis. As a diagnostic lymph node biopsy was performed only after reduction of immunosuppressive therapy, we are able to study the histopathological changes characterizing PTLD regression. We observed extensive apoptosis of blast cells, accompanied by an abundant infiltrate comprising predominantly CD8-positive, Granzyme B-positive T-cells. This observation supports the idea that regression of PTLD is mediated by cytotoxic T-cells and is in keeping with the observation that T-cell depletion, represents a major risk factor for the development of PTLD.

摘要

移植后 EBV 相关 B 细胞淋巴增生性疾病(PTLD)是干细胞移植后的严重并发症。据信,这是由于医源性免疫抑制导致 T 细胞对 EBV 感染的控制放松,从而导致病毒重新激活和 EBV 感染的 B 淋巴细胞增殖。支持这一观点的是,减少免疫抑制治疗可能导致 PTLD 消退。我们报告了一例 18 岁男性,在接受急性淋巴细胞白血病同种异体干细胞移植后 2 个月发生单形性 B 细胞 PTLD。减少免疫抑制治疗导致淋巴结病消退。然而,3 个月后,由于广泛的移植物抗宿主病和败血症,患者死亡。由于仅在减少免疫抑制治疗后进行了诊断性淋巴结活检,我们能够研究特征性 PTLD 消退的组织病理学变化。我们观察到大量胚细胞广泛凋亡,伴有大量浸润细胞,主要为 CD8 阳性、Granzyme B 阳性 T 细胞。这一观察结果支持 PTLD 消退是由细胞毒性 T 细胞介导的观点,并与 T 细胞耗竭是 PTLD 发展的主要危险因素的观察结果一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a81b/2853499/8a39a2c8fd97/1746-1596-5-21-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a81b/2853499/8a39a2c8fd97/1746-1596-5-21-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a81b/2853499/8a39a2c8fd97/1746-1596-5-21-1.jpg

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本文引用的文献

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EBV reactivation and post transplant lymphoproliferative disorders following allogeneic SCT.异基因造血干细胞移植后的EB病毒激活及移植后淋巴增殖性疾病
Bone Marrow Transplant. 2008 Aug;42(3):181-6. doi: 10.1038/bmt.2008.150. Epub 2008 Jun 2.
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Cellular responses to viral infection in humans: lessons from Epstein-Barr virus.人类细胞对病毒感染的反应:来自爱泼斯坦-巴尔病毒的启示。
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