Neval Ete Wareham,Victoria S Kjærgaard,Mohammed Habib,Joanne Reekie,Kasper Rossing,Henrik Sengeløv,Marlyse Buisson,Jean-Luc Lenormand,Michael Perch,Nicolai Schultz,Nikolai Kirkby,Søren S Sørensen,Julien Lupo,Jens D Lundgren,Daniel D Murray,Emmanuel Drouet
{"title":"可溶性eb病毒BZLF1蛋白(sZEBRA)在检测实体器官(SOT)和造血细胞(HSCT)移植后淋巴细胞增生性疾病(PTLD)中的诊断价值","authors":"Neval Ete Wareham,Victoria S Kjærgaard,Mohammed Habib,Joanne Reekie,Kasper Rossing,Henrik Sengeløv,Marlyse Buisson,Jean-Luc Lenormand,Michael Perch,Nicolai Schultz,Nikolai Kirkby,Søren S Sørensen,Julien Lupo,Jens D Lundgren,Daniel D Murray,Emmanuel Drouet","doi":"10.1093/infdis/jiaf477","DOIUrl":null,"url":null,"abstract":"BACKGROUND\r\nPost-transplant lymphoproliferative disorder (PTLD) is a serious complication of solid organ transplant (SOT) and hematopoietic stem cell transplant (HSCT) recipients and is often associated with Epstein-Barr virus (EBV) reactivation. The sZEBRA protein, a soluble form of the EBV nuclear Immediate-early antigen BZLF1 (also called Zta), plays a crucial role in EBV reactivation and immune evasion. This study aimed to externally validate an association between sZEBRA and the diagnosis of PTLD.\r\n\r\nMETHODS\r\nIn this retrospective case-control study, the relative odds of having PTLD according to sZEBRA plasma levels at diagnosis of PTLD and comparable follow-up for controls was analyzed using logistic regression adjusting for demographics, transplant information and sample timing. The model was further also adjusted for corresponding EBV PCR plasma levels. Levels of sZEBRA was fitted in the model either as present/absent or in quartiles.\r\n\r\nRESULTS\r\n33 (17%) PTLD cases and 161 (83%) controls were included. The adjusted odds ratio (aOR) of a positive versus negative sZEBRA test for PTLD diagnosis was 2.82 (95% CI 1.37-7.68); after additional adjustment for EBV PCR levels, the aOR was 4.15 (95% CI 1.31-13.14). Separating sZEBRA levels into quartiles, aOR of sZEBRA in the 4th quartile was 12.43 (95% CI 1.99-77.55) compared to a negative result in the fully adjusted model.\r\n\r\nCONCLUSION\r\nElevated sZEBRA levels, especially those in the highest quartile and when combined with EBV PCR, were associated with PTLD and may serve as a complementary biomarker to EBV PCR to identify patients with PTLD.","PeriodicalId":501010,"journal":{"name":"The Journal of Infectious Diseases","volume":"16 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The diagnostic value of soluble Epstein-Barr Virus BZLF1 protein (sZEBRA) in the Detection of Post-transplant lymphoproliferative Disease (PTLD) among Solid Organ (SOT) and Haematopoietic Cell (HSCT) Transplant Recipients.\",\"authors\":\"Neval Ete Wareham,Victoria S Kjærgaard,Mohammed Habib,Joanne Reekie,Kasper Rossing,Henrik Sengeløv,Marlyse Buisson,Jean-Luc Lenormand,Michael Perch,Nicolai Schultz,Nikolai Kirkby,Søren S Sørensen,Julien Lupo,Jens D Lundgren,Daniel D Murray,Emmanuel Drouet\",\"doi\":\"10.1093/infdis/jiaf477\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"BACKGROUND\\r\\nPost-transplant lymphoproliferative disorder (PTLD) is a serious complication of solid organ transplant (SOT) and hematopoietic stem cell transplant (HSCT) recipients and is often associated with Epstein-Barr virus (EBV) reactivation. The sZEBRA protein, a soluble form of the EBV nuclear Immediate-early antigen BZLF1 (also called Zta), plays a crucial role in EBV reactivation and immune evasion. This study aimed to externally validate an association between sZEBRA and the diagnosis of PTLD.\\r\\n\\r\\nMETHODS\\r\\nIn this retrospective case-control study, the relative odds of having PTLD according to sZEBRA plasma levels at diagnosis of PTLD and comparable follow-up for controls was analyzed using logistic regression adjusting for demographics, transplant information and sample timing. The model was further also adjusted for corresponding EBV PCR plasma levels. Levels of sZEBRA was fitted in the model either as present/absent or in quartiles.\\r\\n\\r\\nRESULTS\\r\\n33 (17%) PTLD cases and 161 (83%) controls were included. The adjusted odds ratio (aOR) of a positive versus negative sZEBRA test for PTLD diagnosis was 2.82 (95% CI 1.37-7.68); after additional adjustment for EBV PCR levels, the aOR was 4.15 (95% CI 1.31-13.14). Separating sZEBRA levels into quartiles, aOR of sZEBRA in the 4th quartile was 12.43 (95% CI 1.99-77.55) compared to a negative result in the fully adjusted model.\\r\\n\\r\\nCONCLUSION\\r\\nElevated sZEBRA levels, especially those in the highest quartile and when combined with EBV PCR, were associated with PTLD and may serve as a complementary biomarker to EBV PCR to identify patients with PTLD.\",\"PeriodicalId\":501010,\"journal\":{\"name\":\"The Journal of Infectious Diseases\",\"volume\":\"16 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-09-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Infectious Diseases\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1093/infdis/jiaf477\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Infectious Diseases","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/infdis/jiaf477","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
移植后淋巴细胞增生性疾病(PTLD)是实体器官移植(SOT)和造血干细胞移植(HSCT)受者的严重并发症,通常与eb病毒(EBV)再激活有关。sZEBRA蛋白是EBV核即刻早期抗原BZLF1(也称为Zta)的可溶性形式,在EBV再激活和免疫逃避中起着至关重要的作用。本研究旨在从外部验证sZEBRA与PTLD诊断之间的关联。方法在本回顾性病例对照研究中,采用logistic回归对人口统计学、移植信息和样本时间进行调整,分析PTLD诊断时sZEBRA血浆水平和对照随访时PTLD发生的相对几率。该模型还进一步调整了相应的EBV PCR血浆水平。sZEBRA的水平以存在/不存在或四分位数的形式拟合在模型中。结果共纳入33例(17%)PTLD患者和161例(83%)对照组。sZEBRA检测阳性与阴性诊断PTLD的校正优势比(aOR)为2.82 (95% CI 1.37-7.68);在进一步调整EBV PCR水平后,aOR为4.15 (95% CI 1.31-13.14)。将sZEBRA水平分成四分位数,第4四分位数的aOR为12.43 (95% CI 1.99-77.55),而完全调整模型的结果为负。结论sZEBRA水平升高,特别是最高四分位的sZEBRA水平升高,与EBV PCR相结合,与PTLD相关,可作为EBV PCR鉴别PTLD患者的补充生物标志物。
The diagnostic value of soluble Epstein-Barr Virus BZLF1 protein (sZEBRA) in the Detection of Post-transplant lymphoproliferative Disease (PTLD) among Solid Organ (SOT) and Haematopoietic Cell (HSCT) Transplant Recipients.
BACKGROUND
Post-transplant lymphoproliferative disorder (PTLD) is a serious complication of solid organ transplant (SOT) and hematopoietic stem cell transplant (HSCT) recipients and is often associated with Epstein-Barr virus (EBV) reactivation. The sZEBRA protein, a soluble form of the EBV nuclear Immediate-early antigen BZLF1 (also called Zta), plays a crucial role in EBV reactivation and immune evasion. This study aimed to externally validate an association between sZEBRA and the diagnosis of PTLD.
METHODS
In this retrospective case-control study, the relative odds of having PTLD according to sZEBRA plasma levels at diagnosis of PTLD and comparable follow-up for controls was analyzed using logistic regression adjusting for demographics, transplant information and sample timing. The model was further also adjusted for corresponding EBV PCR plasma levels. Levels of sZEBRA was fitted in the model either as present/absent or in quartiles.
RESULTS
33 (17%) PTLD cases and 161 (83%) controls were included. The adjusted odds ratio (aOR) of a positive versus negative sZEBRA test for PTLD diagnosis was 2.82 (95% CI 1.37-7.68); after additional adjustment for EBV PCR levels, the aOR was 4.15 (95% CI 1.31-13.14). Separating sZEBRA levels into quartiles, aOR of sZEBRA in the 4th quartile was 12.43 (95% CI 1.99-77.55) compared to a negative result in the fully adjusted model.
CONCLUSION
Elevated sZEBRA levels, especially those in the highest quartile and when combined with EBV PCR, were associated with PTLD and may serve as a complementary biomarker to EBV PCR to identify patients with PTLD.