Epstein-Barr virus infection following allogeneic hematopoietic stem cell transplantation in the era of letermovir for cytomegalovirus prophylaxis

被引:0
作者
Huang, Jingtao [1 ]
Zhou, Jing [2 ]
Zhang, Shixuan [3 ,4 ]
Zhang, Ruoxuan [2 ]
Pan, Zengkai [1 ]
Wang, Luxiang [1 ]
Jiang, Chuanhe [1 ]
Huang, Jiayu [1 ]
Zhang, Zilu [1 ]
Zhao, Yanmin [3 ,4 ]
Cao, Yang [2 ]
Hu, Xiaoxia [1 ]
机构
[1] Shanghai Jiao Tong Univ, Ruijin Hosp, Natl Res Ctr Translat Med Shanghai, Shanghai Inst Hematol,State Key Lab Med Genom,Sch, Shanghai, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Hematol, Wuhan, Hubei, Peoples R China
[3] Zhejiang Univ, Sch Med, Affiliated Hosp 1, Bone Marrow Transplantat Ctr, Hangzhou, Zhejiang, Peoples R China
[4] Zhejiang Univ, Sch Med, Liangzhu Lab, Hangzhou, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Allo-HCT; Letermovir; EBV infection; PTLD; Immune reconstitution;
D O I
10.1186/s40164-025-00665-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Letermovir is an antiviral agent that significantly decreases the frequency of cytomegalovirus (CMV) infections following allogeneic hematopoietic stem cell transplantation (allo-HCT); however, its impact on Epstein-Barr virus (EBV) infection remains unclear. This multicenter, retrospective study involved 565 patients aged >= 18 years, who underwent allo-HCT between January 2021 and December 2023, with 284 receiving letermovir prophylaxis (letermovir group) and 281 not (control group). Cumulative incidences of clinically significant CMV infection (cs-CMVi), EBV DNAemia, EBV-disease and post-transplant lymphoproliferative disorder (PTLD) were compared between the groups. The 1-year cumulative incidence of EBV DNAemia did not differ significantly between the letermovir and control groups (58.1% vs. 52.7%, P = 0.3). However, letermovir prophylaxis was associated with a significantly higher incidence of PTLD within the first year post-HCT (7.39% vs. 1.80%, P = 0.00059). Multivariate analysis identified letermovir prophylaxis as an independent risk factor for PTLD (HR [95% CI]: 4.619 [1.458-10.278], P = 0.007). Letermovir altered the early reconstitution trajectory after allo-HCT, particularly in CD8(+) T cells. Our findings emphasized that although letermovir prophylaxis did not increase the risk of EBV DNAemia in allo-HCT recipients, it was associated with a higher incidence of PTLD. Further studies focusing on immune reconstitutiom dynamics are warranted to elucidate the underlying pathophysiology of EBV-PTLD under letermovir pressure.
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页数:5
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