Wreghitt T
Clinical Microbiology and Public Health Laboratory, Addenbrooke's Hospital, Cambridge, UK.
J Antimicrob Chemother. 1989 Jun;23 Suppl E:49-60. doi: 10.1093/jac/23.suppl_e.49.
Of the first 250 heart and 41 heart-lung transplant recipients in the Papworth series, 244 who survived for longer than one month after transplantation were studied for evidence of cytomegalovirus (CMV) infection by serological methods. Overall, 43 (17.6%) patients acquired primary CMV infection and 76 (31.1%) had evidence of CMV reactivation or reinfection. The source of CMV infection was found to be important. CMV infection was more severe when acquired from the donor organ than from blood or blood products and all seven fatal primary CMV infections were associated with CMV antibody-positive donors. Thus, we now have a CMV matching policy in our unit; whenever possible organs from CMV antibody-positive donors are not given to CMV antibody-negative recipients. Those CMV antibody-positive recipients who received organs from CMV antibody-positive donors had more severe CMV reactivation or reinfection than those who received organs from CMV antibody-negative donors. The severity of CMV disease was found to be dependent on the degree of immunosuppression patients received and heart-lung transplant recipients had more serious CMV infections than heart transplant patients. The severity of CMV infections in heart-lung transplant recipients was modified in the later part of the series by the use of prophylactic anti-CMV hyperimmune globulin and treatment of CMV infection with ganciclovir. While 75% of heart-lung transplant recipients who did not receive this treatment died of primary donor-acquired CMV infection, all three comparable patients given CMV hyperimmune globulin and ganciclovir survived. The outcome of CMV infections in the Papworth heart and heart-lung transplant recipients is compared with that in other comparable transplant centres.
在帕普沃思系列研究的首批250例心脏移植受者和41例心肺移植受者中,对移植后存活超过1个月的244例患者采用血清学方法研究巨细胞病毒(CMV)感染证据。总体而言,43例(17.6%)患者发生原发性CMV感染,76例(31.1%)有CMV再激活或再感染证据。发现CMV感染的来源很重要。从供体器官获得的CMV感染比从血液或血液制品获得的更严重,所有7例致命的原发性CMV感染均与CMV抗体阳性供体有关。因此,我们科室现在有一项CMV配型政策;只要有可能,不将来自CMV抗体阳性供体的器官给予CMV抗体阴性受者。那些接受来自CMV抗体阳性供体器官的CMV抗体阳性受者,其CMV再激活或再感染比接受来自CMV抗体阴性供体器官的受者更严重。发现CMV疾病的严重程度取决于患者接受的免疫抑制程度,心肺移植受者的CMV感染比心脏移植患者更严重。在该系列研究的后期,通过使用预防性抗CMV高效价免疫球蛋白和用更昔洛韦治疗CMV感染,改变了心肺移植受者CMV感染的严重程度。未接受这种治疗的心肺移植受者中有75%死于原发性供体获得性CMV感染,而给予CMV高效价免疫球蛋白和更昔洛韦的3例对照患者均存活。将帕普沃思心脏和心肺移植受者中CMV感染的结果与其他类似移植中心的结果进行了比较。