Zekri Abdel-Rahman N, Mohamed Waleed S, Samra Mohamed A, Sherif Ghada M, El-Shehaby Amal M R, El-Sayed Manal H
Virology and Immunology Unit, Cancer Biology Department, National Cancer Institute, Fom El-Khalig, Cairo 11796, Egypt.
Transpl Immunol. 2004 Dec;13(4):305-11. doi: 10.1016/j.trim.2004.10.001.
To derive guidelines for a safer bone marrow transplantation (BMT) policy, we have to study pre-BMT risk factors that may be associated with an increased post-BMT death. Among those factors, the importance of pre-BMT viral hepatitis markers in BMT donors and recipients remains unsettled. In the present study, we have determined the effect of prior donor and recipient cytomegalovirus (CMV), hepatitis B virus (HBV), and hepatitis C virus (HCV) exposure on the incidence of those viral infections after bone marrow transplantation (BMT). The study included 63 patients presented to the BMT unit; 28 of them underwent transplantation and 35 were not transplanted. All serum markers of CMV, HBV, and HCV infections were monitored using ELISA technique, as well as PCR-DNA for CMV, HBV and HCV RT-PCR techniques for HCV. The incidence of active CMV and HCV was 11/28 (39%) and 6/28 (21%) in post-BMT recipients compared to 2/35 (6%) and 2/35 (6%) in the 35 untransplanted patients (P=0.00003 and P=0.05). Whereas active HBV infection was non significantly (P=0.13) higher 3/28 (11%) in the BMT patients in comparison to 1/35 (3%) in untransplanted patients. Ten out of the 19 (53%) of the CMV-seropositive recipients developed CMV reactivation compared to 1/9 (11%) of the CMV-seronegative recipients who developed CMV seroconversion. In addition, 3/8 (38%) of the HBV-seropositive recipients developed HBV reactivation in comparison to 0/20 of the HBV-seronegative recipients. Moreover, 5/13 (39%) of the HCV-seropositive recipients developed HCV reactivation in comparison to 1/16 (6%) of the HCV-seronegative recipients who developed HCV seroconversion. In conclusion, previous exposure to CMV, HBV, and HCV infections in the recipients of BMT patients were found to influence the risk of developing those viral infections.
为制定更安全的骨髓移植(BMT)政策指南,我们必须研究可能与BMT后死亡风险增加相关的BMT前危险因素。在这些因素中,BMT供者和受者的BMT前病毒性肝炎标志物的重要性仍未明确。在本研究中,我们确定了供者和受者既往巨细胞病毒(CMV)、乙型肝炎病毒(HBV)和丙型肝炎病毒(HCV)感染对骨髓移植(BMT)后这些病毒感染发生率的影响。该研究纳入了63名到BMT科室就诊的患者;其中28人接受了移植,35人未接受移植。使用ELISA技术监测CMV、HBV和HCV感染的所有血清标志物,以及用于CMV的PCR-DNA、用于HBV的PCR技术和用于HCV的HCV RT-PCR技术。BMT后受者中活动性CMV和HCV的发生率分别为11/28(39%)和6/28(21%),而35名未移植患者中分别为2/35(6%)和2/35(6%)(P=0.00003和P=0.05)。而BMT患者中活动性HBV感染率为3/28(11%),略高于未移植患者中的1/35(3%),但差异无统计学意义(P=0.13)。19名CMV血清阳性受者中有10名(53%)发生了CMV再激活,而9名CMV血清阴性受者中只有1名(11%)发生了CMV血清转化。此外,8名HBV血清阳性受者中有3名(38%)发生了HBV再激活,而20名HBV血清阴性受者中无1名发生。此外,13名HCV血清阳性受者中有5名(39%)发生了HCV再激活,而16名HCV血清阴性受者中只有1名(6%)发生了HCV血清转化。总之,发现BMT患者受者既往接触CMV、HBV和HCV感染会影响发生这些病毒感染的风险。