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首页> 外文期刊>BMC Infectious Diseases >Disseminated cytomegalovirus disease after bendamustine: a case report and analysis of circulating B- and T-cell subsets
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Disseminated cytomegalovirus disease after bendamustine: a case report and analysis of circulating B- and T-cell subsets

机译:苯达莫司汀后传播的巨细胞病毒病:一例病例报告和循环B细胞和T细胞亚群分析

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Bendamustine, used for the treatment of indolent B-cell non-Hodgkin lymphoma and chronic lymphocytic leukemia, is known to cause prolonged myelosuppression and lymphocytopenia and has been associated with the risk of developing serious and fatal infections. While reports of localized CMV infections in asymptomatic patients exist, disseminated CMV disease has not been described. We report the first case of disseminated CMV infection in a 75-year-old male diagnosed with lymphoplasmacytic lymphoma/Waldenstr?m macroglobulinemia with massive bone marrow infiltration. Despite 6-cycle R-bendamustine chemotherapy resulted in a good partial response, the patient developed persistent fever and severe weight loss. Analysis of cerebrospinal fluid and peripheral blood revealed the presence of CMV-DNA, while the fundus oculi examination revealed bilateral CMV retinitis. Treatment with induction and maintenance drugs was complicated by neutropenia and deterioration of renal function with electrolyte imbalance. From an immunological standpoint, we observed a profound imbalances in phenotype and function of B- and T-cell subsets, with a high proportion of circulating total, activated CD69+ and CD80+ B-cells, a low γ/δ T-cell frequency with a high proportion of CD69- and CD38-expressing cells, and hyperactivated/exhausted CD4+ and CD8+ T-cell phenotypes unable to face CMV challenge. We hereby describe a severe form of disseminated CMV disease after R-bendamustine treatment. Our observations strongly support the careful clinical monitoring of CMV reactivation/infection in oncologic patients undergoing this therapeutic regimen.
机译:苯达莫司汀用于治疗惰性B细胞非霍奇金淋巴瘤和慢性淋巴细胞性白血病,已知会导致长时间的骨髓抑制和淋巴细胞减少,并与发展严重和致命感染的风险有关。尽管无症状患者存在局部CMV感染的报道,但尚未描述传播性CMV疾病。我们报告了第一例传播性巨细胞病毒感染的病例,该患者是一名75岁的男性,被诊断为具有大量骨髓浸润的淋巴浆细胞性淋巴瘤/ Waldenstr?m巨球蛋白血症。尽管进行了6个周期的R-苯达莫司汀化疗导致了良好的部分反应,但患者仍持续发烧并严重体重减轻。脑脊液和外周血的分析显示存在CMV-DNA,而眼底检查则显示双侧CMV视网膜炎。中性粒细胞减少症和电解质功能失衡导致肾功能恶化使使用诱导和维持药物的治疗复杂化。从免疫学的角度来看,我们观察到B细胞和T细胞亚型的表型和功能存在严重的失衡,其中循环中的活化CD69 +和CD80 + B细胞比例很高,γ/δT细胞频率低,高比例的CD69和CD38表达细胞,以及过度活化/耗尽的CD4 +和CD8 + T细胞表型无法应对CMV挑战。我们在此描述R-苯达莫司汀治疗后的一种严重形式的传播性CMV疾病。我们的观察结果强烈支持对接受此治疗方案的肿瘤患者进行CMV重新激活/感染的仔细临床监测。

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