Cytomegalovirus Infection and Rates of Antiviral Resistance Following Intestinal and Multivisceral Transplantation

被引:19
作者
Ambrose, T. [1 ]
Sharkey, L. M. [1 ]
Louis-Auguste, J. [1 ]
Rutter, C. S. [1 ]
Duncan, S. [1 ]
English, S. [2 ]
Gkrania-Klotsas, E. [3 ]
Carmichae, A. [3 ]
Woodward, J. M. [1 ]
Russell, N. [4 ]
Massey, D. [1 ]
Butler, A. [4 ]
Middleton, S. [1 ]
机构
[1] Addenbrookes Hosp, Dept Gastroenterol, Box 133,Hills Rd, Cambridge CB2 2QQ, England
[2] Addenbrookes Hosp, Dept Clin Virol, Box 133,Hills Rd, Cambridge CB2 2QQ, England
[3] Addenbrookes Hosp, Dept Infect Dis, Box 133,Hills Rd, Cambridge CB2 2QQ, England
[4] Addenbrookes Hosp, Dept Transplant Surg, Box 133,Hills Rd, Cambridge CB2 2QQ, England
基金
英国医学研究理事会;
关键词
T-CELL IMMUNOTHERAPY; CMV DISEASE; RISK-FACTORS; GANCICLOVIR; PREVENTION; EFFICACY; VALGANCICLOVIR; MANAGEMENT; PATIENT;
D O I
10.1016/j.transproceed.2015.09.070
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Cytomegalovirus (CMV) disease is a common and clinically significant complication following intestinal or multivisceral transplantation. CMV disease is more common in cases of serologic mismatch between donor and recipient. Though in some cases it may be asymptomatic, in the immunosuppressed population it often manifests with evidence of systemic infection or end-organ disease. Methods. We conducted a retrospective review of all patients undergoing intestinal or multivisceral transplantation over 8 years at our institution. Results. Forty-eight transplantations were performed, with 40% of the patients (19/48) having >= 1 episode of CMV viremia, which rose to 90% in the "donor-positive, recipient-negative" (DPRN) serologic mismatch group. The median time to 1st episode following transplantation was 22.3 weeks (range, 1-78) and median duration of each episode was 4.9 weeks (range, 1.6-37.4). Six of the 19 viremic patients (31.6%) developed virologic resistance with 4 of these occurring in the DPRN group. Four of the 6 patients with drug resistant CMV died with CMV viremia. All patients with drug resistance acquired ganciclovir resistance; these patients were more challenging to manage with second-line toxicity-limited treatments, including foscarnet, cidofovir, and leflunomide. CMV immunoglobulin has been used and we briefly discuss the use of CMV-specific adoptive T-lymphocyte transfer in the management of 1 case. Conclusions. Post-transplantation CMV disease continues to be challenging to manage, and there is little consensus on optimal management strategies in this patient group, with a significant requirement for novel therapies; these may be pharmacologic or cell based. Extensive multidisciplinary discussion is important for most cases, but particularly for those patients who acquire virologic resistance.
引用
收藏
页码:492 / 496
页数:5
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