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慢性活动性 EB 病毒感染中经第二次异基因造血干细胞移植成功治疗的 NK 细胞移植后淋巴增殖性疾病

英文原题:NK-cell post-transplant lymphoproliferative disease successfully treated by second allogenic hematopoietic stem cell transplantation in chronic active Epstein-Barr virus infection.

查看英文原题

NK-cell post-transplant lymphoproliferative disease successfully treated by second allogenic hematopoietic stem cell transplantation in chronic active Epstein-Barr virus infection.

PubMed 2022/01/10(内容时间) Int J Hematol Q3 · IF 1.9(JCR 2025)

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中文摘要

慢性活动性Epstein-Barr病毒感染(CAEBV)是一种由EB病毒(EBV)引起的系统性T细胞或自然杀伤(NK)细胞淋巴增殖性疾病(LPD)。异基因造血干细胞移植(HSCT)是CAEBV唯一的根治性治疗,但仍可能复发。复发通常被认为与受者来源的CAEBV细胞增殖有关。本文报告一例病例:一名41岁女性因CAEBV接受HLA匹配的同胞供者首次异基因HSCT后,发生供者来源的CAEBV样NK细胞移植后淋巴增殖性疾病(PTLD)。随后接受HLA匹配的无关供者第二次HSCT,疾病得到控制,但仍持续检测到第二位供者来源细胞感染EBV。尽管CAEBV及CAEBV样NK细胞PTLD的发病机制尚未得到详细阐明,本病例提示,包括家族因素在内的宿主遗传因素可能参与疾病发生。

展开英文摘要原文

Chronic active Epstein-Barr virus infection (CAEBV) is a systemic T- or NK-lymphoproliferative disorder (LPD) caused by EBV. Allogenic hematopoietic stem cell transplantation (HSCT) is the only curative therapy for CAEBV, but relapse sometimes occurs. Relapse is generally attributed to proliferation of recipient-derived CAEBV cells.

We herein report a case of donor-derived CAEBV-like NK-cell post-transplant lymphoproliferative disease (PTLD) in a 41-year-old female after the first allogenic HSCT for CAEBV from an HLA-matched sibling donor. A second HSCT from an HLA-matched unrelated donor successfully controlled the disease, but EBV infection of cells derived from the second donor continued to be detected.

Although the mechanisms underlying CAEBV and CAEBV-like NK-cell PTLD have not yet been elucidated in detail, the findings of the present case imply that host genetic factors, including familial factors, may be important in disease development.

论文信息

作者
Shibata S、Takiuchi Y、Kawasaki N、Okamoto Y、Inano S、Fukunaga A、Tabata S、Arai A
第一作者单位
Department of Hematology, Kitano hospital, Medical Research Institute, 2-4-20, Ougimachi, Kita-ku, Osaka, Japan.Japan
通讯作者单位
Department of Hematology, Kitano hospital, Medical Research Institute, 2-4-20, Ougimachi, Kita-ku, Osaka, Japan. youtak@kuhp.kyoto-u.ac.jp.Japan
文献类型
病例报告
期刊
International journal of hematology2022 Apr
原文标识
PubMed 35001347 · DOI 10.1007/s12185-021-03271-y