Virology Division, Department of Microbiology, SEALS, Prince of Wales Hospital, Sydney, Australia.
J Clin Virol. 2011 Aug;51(4):229-33. doi: 10.1016/j.jcv.2011.05.012. Epub 2011 Jun 8.
Cytomegalovirus (CMV) remains the leading viral cause of disease following orthotopic liver transplantation (OLT) despite the availability of antiviral agents for prophylaxis and therapy.
Examine the viral factors that influence the outcome of CMV infection following valganciclovir prophylaxis or laboratory-guided preemptive therapy in OLT recipients.
The value of valganciclovir prophylaxis and laboratory-guided preemptive therapy for the prevention of CMV infection and disease was observed in 64 OLT recipients. Prophylaxis was given to all CMV seronegative recipients receiving a liver from a seropositive donor (D+R-; n=15), and all other recipients were randomised to receive either prophylaxis (n=24) or laboratory-guided preemptive therapy (n=25). Recipients were monitored for CMV DNAemia, viral load, emergence of antiviral resistant strains and co-infections.
CMV end-organ disease and antiviral resistant strains only occurred in D+R- recipients despite the use of prophylaxis in these patients. The D+R- recipients commencing prophylaxis immediately following transplantation had better outcomes compared to those for whom prophylaxis was delayed due to renal impairment. Prophylaxis reduced the incidence of CMV DNAemia, persistent infection, and high viral loads for CMV seropositive (D-R+and D+R+) recipients, but laboratory-guided preemptive therapy effectively controlled CMV infection and prevented disease in these OLT recipients.
Delaying the commencement of valganciclovir prophylaxis may be associated with worse outcomes for high-risk OLT recipients. Laboratory-guided pre-emptive therapy remains an alternative approach for seropositive recipients at lower risk of CMV disease.
尽管有抗病毒药物用于预防和治疗,但巨细胞病毒(CMV)仍然是原位肝移植(OLT)后疾病的主要病毒原因。
研究影响 OLT 受者更昔洛韦预防或实验室指导的抢先治疗后 CMV 感染结局的病毒因素。
观察了 64 名 OLT 受者使用缬更昔洛韦预防和实验室指导的抢先治疗预防 CMV 感染和疾病的效果。所有接受 CMV 血清阴性供体(D+R-;n=15)肝脏的受者均给予预防治疗,所有其他受者随机接受预防治疗(n=24)或实验室指导的抢先治疗(n=25)。监测受者 CMV DNA 血症、病毒载量、抗病毒耐药株和合并感染的情况。
尽管这些患者使用了预防治疗,但只有 D+R-受者才会发生 CMV 终末器官疾病和抗病毒耐药株。与因肾功能损害而延迟预防治疗的患者相比,立即在移植后开始预防治疗的 D+R-受者结局更好。预防治疗降低了 CMV 血清阳性(D-R+和 D+R+)受者 CMV DNA 血症、持续感染和高病毒载量的发生率,但实验室指导的抢先治疗有效地控制了这些 OLT 受者的 CMV 感染并预防了疾病。
延迟开始缬更昔洛韦预防治疗可能与高危 OLT 受者的结局更差有关。对于 CMV 疾病风险较低的血清阳性受者,实验室指导的抢先治疗仍然是一种替代方法。