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病例报告:造血干细胞移植后肝移植中肝脏作为造血干细胞来源

Case Report: Liver as a Source of Hematopoietic Stem Cells After Liver Transplantation Following Hematopoietic Stem Cell Transplantation.

作者信息

Jarmoliński Tomasz, Rosa Monika, Rybka Blanka, Ryczan-Krawczyk Renata, Gajek Kornelia, Bogunia-Kubik Katarzyna, Klaudel-Dreszler Maja, Czubkowski Piotr, Kaliciński Piotr, Teisseyre Joanna, Stefanowicz Marek, Gorczyńska Ewa, Kałwak Krzysztof, Ussowicz Marek

机构信息

Department and Clinic of Pediatric Oncology, Hematology and Bone Marrow Transplantation, Wrocław Medical University, Wrocław, Poland.

Laboratory of Clinical Immunogenetics and Pharmacogenetics, Laboratory of Tissue Immunology of the Medical Center, Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland.

出版信息

Front Pediatr. 2022 Mar 23;10:861692. doi: 10.3389/fped.2022.861692. eCollection 2022.

Abstract

We report a child with Fanconi anemia who, after hematopoietic stem cell transplantation (HSCT) complicated by acute graft-versus-host disease (GVHD), underwent orthotopic liver transplantation (OLT). Approximately 1 month after OLT, the presence of third-party genetic material from the liver donor was noted and in the next few weeks, the chimerism assessment revealed 100% liver donor leukocytes in the peripheral blood. The rapidly progressing GVHD with gut involvement resulted in patient's death 6 months after OLT. The liver can act as a clinically significant source of hematopoietic stem cells, and the liver donor's young age must be emphasized as potentially predisposing to this phenomenon. Transfer of OLT hematopoietic stem cells may not have clinical significance unless the patient is not immunocompetent or develops liver-transplantation associated GVHD, that can result in lymphocyte mediated elimination of original hematopoiesis. Patients with preexisting immunity disorder (such as primary or secondary immunodeficiency) might require intensified immunosuppressive therapy in peritransplant period as a prevention of liver-transplantation associated GVHD. Close monitoring of hematopoietic chimerism after OLT is warranted in patients at risk, because cytopenia or OLT hematopoiesis can reflect subclinical GVHD and further studies are necessary to elucidate this phenomenon.

摘要

我们报告了一名患有范可尼贫血的儿童,该患儿在造血干细胞移植(HSCT)并发急性移植物抗宿主病(GVHD)后,接受了原位肝移植(OLT)。OLT术后约1个月,发现外周血中存在来自肝脏供体的第三方遗传物质,在接下来的几周内,嵌合体评估显示外周血中100%为肝脏供体白细胞。快速进展且累及肠道的GVHD导致患者在OLT术后6个月死亡。肝脏可成为具有临床意义的造血干细胞来源,必须强调肝脏供体年龄较小可能是导致这一现象的潜在因素。OLT造血干细胞的转移可能没有临床意义,除非患者免疫功能不全或发生与肝移植相关的GVHD,后者可导致淋巴细胞介导的原始造血消除。患有既往免疫障碍(如原发性或继发性免疫缺陷)的患者在移植期间可能需要强化免疫抑制治疗,以预防与肝移植相关的GVHD。对于有风险的患者,OLT术后密切监测造血嵌合体是必要的,因为血细胞减少或OLT造血可能反映亚临床GVHD,需要进一步研究以阐明这一现象。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c97/8984257/52f0e7b4d84e/fped-10-861692-g001.jpg

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