Factors Associated with Cytomegalovirus Reactivation Following Allogeneic Hematopoietic Stem Cell Transplantation: Human Leukocyte Antigens Might Be Among the Risk Factors

被引:1
作者
Acar, Kadir [1 ]
Aki, Sahika Zeynep [1 ]
Ozkurt, Zubeyde Nur [1 ]
Bozdayi, Gulendam [2 ]
Rota, Seyyal [2 ]
Sucak, Gulsan Turkoz [1 ]
机构
[1] Gazi Univ, Fac Med, Dept Hematol, Ankara, Turkey
[2] Gazi Univ, Fac Med, Dept Microbiol, Ankara, Turkey
关键词
Cytomegalovirus reactivation; Human leukocyte antigens; Allogeneic stem cell transplantation; Graft-versus-host disease; Prognosis; CMV scoring index; CYTOTOXIC T-LYMPHOCYTES; VERSUS-HOST-DISEASE; ADOPTIVE IMMUNOTHERAPY; PREEMPTIVE GANCICLOVIR; PREGNANT-WOMEN; CMV INFECTION; VIRUS; DONOR; RECIPIENT; PROPHYLAXIS;
D O I
10.4274/Tjh.2013.0244
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Cytomegalovirus (CMV) is a significant cause of morbidity and mortality in allogeneic hematopoietic stem cell transplantation (AHSCT) recipients. Current practice includes prophylactic and preemptive treatment modalities, which have risks, side effects, and costs of their own. There is no established risk scoring system that applies to all patients. We aimed to investigate the risk factors for CMV reactivation in AHSCT recipients. Materials and Methods: We retrospectively analyzed the risk factors for CMV reactivation in 185 consequent AHSCT recipients transplanted between September 2003 and December 2009 at the Stem Cell Transplantation Unit of Gazi University. Besides the standard transplant-related parameters, HLA antigens were also included among the variables analyzed. Results: Despite the very high rate of donor (94.6%) and recipient (100%) seropositivity, which are the so-called major risk factors in previous reports, our reactivation rate was much lower, with a frequency of 24.9%. The underlying disease, sex, conditioning regimen, and presence of antithymocyte globulin or fludarabine in the conditioning regimen had no impact on reactivation rate. CMV reactivation was significantly more frequent in recipients with graft-versus-host disease (GVHD) compared to those without GVHD (p<0.0001). CMV reactivation was significantly more frequent (p<0.05) in patients with HLA-B14, HLA-DRB1*01, and HLA-DRB1*13 antigens and less frequent in recipients with HLA-A11 and HLA-DRB1*04 antigens (p<0.05). Conclusion: Universal risk factors/scores that apply to all transplant recipients are required for tailored prophylaxis and/or treatment strategies for CMV reactivation. Uncovering the role of genetic factors, including HLA antigens, as possible risk factors might lead the way to risk-adaptive strategies for adoptive cellular therapy and/or vaccination.
引用
收藏
页码:276 / 285
页数:10
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