Mousavi-Jazi M, Hökeberg I, Schloss L, Zweygberg-Wirgart B, Grillner L, Linde A, Brytting M
Department of Virology, Swedish Institute for Infectious Disease Control, Solna, Sweden.
Transpl Infect Dis. 2001 Dec;3(4):195-202. doi: 10.1034/j.1399-3062.2001.30403.x.
The frequency of infections caused by drug-resistant cytomegalovirus (CMV) in solid-organ transplant recipients is not known. Only a few resistant strains have been described in transplant recipients. Antiviral susceptibility to ganciclovir (GCV) and foscarnet (PFA) of CMV isolates from 24 renal transplant patients with CMV viremia and CMV disease before and after therapy were investigated by a solid phase ELISA. The CMV DNA polymerase (UL54) and viral phosphotransferase (UL97) genes were also sequenced. Ten patients did not receive antiviral treatment; five and nine patients were treated with PFA and GCV, respectively. No appearance of drug-resistant viruses was observed in the present study, but one isolate showed a reduced sensitivity to PFA after treatment with GCV. This finding could not be explained by the presence or development of mutations that have been associated with drug resistance in UL54. We found no evidence that short-term treatment of CMV with PFA- or GCV-induced resistance.
实体器官移植受者中由耐药巨细胞病毒(CMV)引起的感染频率尚不清楚。在移植受者中仅描述了少数耐药菌株。通过固相酶联免疫吸附测定法(ELISA)研究了24例肾移植患者在治疗前后患有CMV病毒血症和CMV疾病的CMV分离株对更昔洛韦(GCV)和膦甲酸钠(PFA)的抗病毒敏感性。还对CMV DNA聚合酶(UL54)和病毒磷酸转移酶(UL97)基因进行了测序。10例患者未接受抗病毒治疗;5例和9例患者分别接受了PFA和GCV治疗。在本研究中未观察到耐药病毒的出现,但有1株分离株在接受GCV治疗后对PFA的敏感性降低。这一发现无法用与UL54中耐药相关的突变的存在或发生来解释。我们没有发现证据表明用PFA或GCV对CMV进行短期治疗会诱导耐药。