Peterson Michael R, Emery Shawn C, Yung Gordon L, Masliah Eliezer, Yi Eunhee S
Department of Pathology, University of California, Medical Center, San Diego, CA 92103-8720, USA.
Arch Pathol Lab Med. 2006 Feb;130(2):176-80. doi: 10.5858/2006-130-176-EVPLDF.
Posttransplantation lymphoproliferative disorder (PTLD) in patients who have undergone solid organ transplantation is thought to be mostly of host (ie, transplant recipient) origin, as opposed to being predominantly of donor origin, which is observed in patients who have undergone bone marrow transplantation. Donor-origin PTLDs reportedly follow a more indolent course than host-origin PTLDs.
To determine the origin of PTLD and its clinical implications in patients who have undergone lung transplantation.
Patients' medical records were reviewed for clinical data. We performed a molecular study to determine the origin of abnormal lymphoid cells in 4 PTLD cases identified from our autopsy files. Each case underwent restriction fragment length polymorphism analysis using polymerase chain reaction-based genotyping for CYP2D6. Epstein-Barr virus (latent membrane protein 1) immunostaining and polymerase chain reaction analysis were performed on PTLD-involved tissues.
Three of 4 PTLD cases were of host origin, and the remaining case was of donor origin. Epstein-Barr virus was detected by immunohistochemical and polymerase chain reaction methods in all PTLD-involved tissues that were examined. There was no apparent difference in clinical manifestations between host-origin and donor-origin PTLD cases in our study.
The PTLDs in our patients who had undergone lung transplantation were Epstein-Barr virus-positive and mostly of host origin, without any notable clinical difference from donor-origin PTLD.
实体器官移植患者发生的移植后淋巴细胞增生性疾病(PTLD)被认为大多起源于宿主(即移植受者),这与骨髓移植患者中主要起源于供者的情况相反。据报道,供者起源的PTLD病程比宿主起源的PTLD更为惰性。
确定肺移植患者中PTLD的起源及其临床意义。
查阅患者病历以获取临床数据。我们对从尸检档案中确定的4例PTLD病例进行了分子研究,以确定异常淋巴细胞的起源。每例病例均使用基于聚合酶链反应的CYP2D6基因分型进行限制性片段长度多态性分析。对PTLD累及组织进行了爱泼斯坦-巴尔病毒(潜伏膜蛋白1)免疫染色和聚合酶链反应分析。
4例PTLD病例中有3例起源于宿主,其余1例起源于供者。在所有接受检查的PTLD累及组织中,通过免疫组织化学和聚合酶链反应方法检测到爱泼斯坦-巴尔病毒。在我们的研究中,宿主起源和供者起源的PTLD病例在临床表现上没有明显差异。
我们的肺移植患者中的PTLD为爱泼斯坦-巴尔病毒阳性,且大多起源于宿主,与供者起源的PTLD在临床上没有显著差异。