Wolf Dana G, Lurain Nell S, Zuckerman Tsila, Hoffman Ron, Satinger Judith, Honigman Alik, Saleh Niveen, Robert Emanuel S, Rowe Jacob M, Kra-Oz Zipora
Hadassah University Hospital, Jerusalem, Israel.
Blood. 2003 Jan 15;101(2):463-5. doi: 10.1182/blood-2002-07-1982. Epub 2002 Aug 22.
Preemptive ganciclovir therapy has reduced the occurrence of early cytomegalovirus (CMV) disease after hematopoietic stem cell (HSC) transplantation. However, late disease is increasingly reported. We describe 2 patients who developed late CMV central nervous system (CNS) disease after haploidentical HSC transplantation. Direct genotypic analysis was used to examine the presence of ganciclovir resistance. One patient had a mixed viral population in the cerebrospinal fluid (CSF), with coexistent wild-type and mutant UL97 sequences. The presence of 2 different strains was confirmed by subclone sequencing of the UL54 gene. One of the strains was different from the concurrent blood strain. The second patient had resistant variant in the lungs. These cases raise concern about the changing natural history of CMV disease in HSC transplantation, with emergence of previously uncommon manifestations following prolonged prophylaxis. Under these circumstances the CNS may be a sanctuary site, where viral persistence and antiviral drug resistance could result from limited drug penetration.
抢先使用更昔洛韦治疗已降低了造血干细胞(HSC)移植后早期巨细胞病毒(CMV)疾病的发生率。然而,晚期疾病的报道日益增多。我们描述了2例在单倍体HSC移植后发生晚期CMV中枢神经系统(CNS)疾病的患者。采用直接基因分型分析来检测更昔洛韦耐药性的存在。1例患者脑脊液(CSF)中存在混合病毒群体,同时存在野生型和突变型UL97序列。通过对UL54基因进行亚克隆测序证实了2种不同毒株的存在。其中一种毒株与同时期血液中的毒株不同。第2例患者肺部存在耐药变异株。这些病例引发了人们对HSC移植中CMV疾病自然史变化的关注,长期预防后出现了以前不常见的表现。在这种情况下,中枢神经系统可能是一个庇护场所,药物渗透受限可能导致病毒持续存在和抗病毒药物耐药性。