再生障碍性贫血
巨细胞病毒
免疫学
球蛋白
病毒学
医学
病毒
爱泼斯坦-巴尔病毒
疱疹病毒科
病毒性疾病
骨髓
作者
Sung‐Soo Park,Sung‐Yeon Cho,Eunhee Han,Gi June Min,Silvia Park,Jae‐Ho Yoon,Sung‐Eun Lee,Byung‐Sik Cho,Ki‐Seong Eom,Yoo‐Jin Kim,Seok Lee,Hee‐Je Kim,Chang‐Ki Min,Seok‐Goo Cho,Jong Wook Lee
摘要
This study aimed to identify the natural course of cytomegalovirus (CMV)/Epstein-Barr virus (EBV) after rabbit antithymocyte globulin and cyclosporine (rATG-CsA) for aplastic anemia (AA).In 113 prospectively observed AA patients treated with rATG-CsA, the CMV/EBV cohort was classified into two groups by baseline viremic status: no viremia (CMV-G1, n = 112; EBV-G1, n = 98) and the presence of viremia (CMV-G2, n = 1; EBV-G2, n = 13).In CMV-G1, the mean CMV load increased up to 3 months but was completely resolved from 6 months. The mean EBV load of EBV-G1 showed a peak at 1 month and then gradually decreased over time but remained detectable throughout the observation period. EBV-G2 showed fluctuating EBV dynamics. With reactivation rates of 38.4% in CMV-G1 and 62.2% in EBV-G1, a longer time to rATG-CsA from diagnosis and a lower absolute lymphocyte count at 1 month from rATG-CsA were significantly associated with CMV and EBV reactivation, respectively. The mean peak CMV and EBV loads of patients with CMV-related (3.5%) and EBV-related (0.9%) diseases were evidently higher than those of the remaining patients without CMV and EBV diseases in the respective cohort.Considering frequent reactivation and distinct courses of CMV/EBV, virologic surveillance is recommended after rATG-CsA for AA.
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