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Effects of Low-Dose Rituximab Therapy in Patients With Primary Cytomegalovirus Infection

机译:小剂量利妥昔单抗治疗对原发性巨细胞病毒感染患者的影响

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Objectives: Cytomegalovirus infection is an im-portant cause of morbidity and mortality among recipients undergoing hematopoietic stem cell and solid-organ transplant. The risk of cytomegalovirus infection is high in cytomegalovirus -seronegative recipients of cytomegalovirus -seropositive organs (donor positive/recipient negative) and recipients with strong immunosuppressive status such as those receiving rituximab induction or antirejection treatment. However, it remains unclear how rituximab affects patients with primary cyto-megalovirus infection. We evaluated the effects of low-dose rituximab therapy on clinical and immunologic outcomes in recipients who were donor positive but recipient negative for primary cytomegalovirus infections. Materials and Methods: We conducted a retro-spective review of patients with primary cyto-megalovirus infections from January 2005 to March 2014. Patient outcomes were compared between groups administered given rituximab or given no intervention at the time of transplant. Results: Our study group included 49 recipients with primary cytomegalovirus infection, including 32 who received rituximab therapy (group 1) and 17 who did not (group 2). No significant differences were observed between groups in the duration of cytomegalovirus seroconversion ( P = .0570) and initial cytomegalovirus immunoglobulin G titers ( P = .8418). Conclusions: Rituximab induction therapy does not affect clinical or immunologic outcomes of primary cytomegalovirus infection, even in high-risk recipients who are donor positive but recipient negative for primary cytomegalovirus infections.
机译:目的:巨细胞病毒感染是接受造血干细胞和实体器官移植的患者发病和死亡的重要原因。巨细胞病毒血清反应阳性器官(供体阳性/受体阴性)的巨细胞病毒血清阴性受体和免疫抑制状态强的接受者,如接受利妥昔单抗诱导或抗排斥治疗的患者,发生巨细胞病毒感染的风险较高。但是,尚不清楚利妥昔单抗如何影响原发性巨细胞病毒感染的患者。我们评估了低剂量利妥昔单抗治疗对原发性巨细胞病毒感染呈供体阳性但呈阴性的受体的临床和免疫结果的影响。材料和方法:我们对2005年1月至2014年3月期间原发性巨细胞病毒感染的患者进行了回顾性研究。比较了接受利妥昔单抗治疗或移植时未进行干预的两组患者的结局。结果:我们的研究组包括49位原发性巨细胞病毒感染的接受者,其中32位接受了利妥昔单抗治疗(第1组)和17位未接受利妥昔单抗治疗(第2组)。在巨细胞病毒血清转化持续时间(P = .0570)和初始巨细胞病毒免疫球蛋白G滴度(P = .8418)之间,两组之间没有观察到显着差异。结论:利妥昔单抗诱导疗法不影响原发性巨细胞病毒感染的临床或免疫学结果,即使在高风险接受者中,原发性巨细胞病毒感染的供者为阳性但接受者为阴性。

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