Klinická rezistence lidského cytomegaloviru při léčbě gancyklovirem u pacientů po alogenní transplantaci hematopoetických buněk--zkušenosti jednoho centra
[Ganciclovir treatment failure in adult allogeneic hematopoietic stem cell transplant recipients with cytomegalovirus infection--a single centre experience]
Jazyk čeština Země Česko Médium print
Typ dokumentu časopisecké články
PubMed
26448304
PII: 56018
- MeSH
- antivirové látky terapeutické užití MeSH
- cytomegalovirové infekce farmakoterapie etiologie virologie MeSH
- Cytomegalovirus účinky léků genetika růst a vývoj fyziologie MeSH
- dospělí MeSH
- ganciklovir terapeutické užití MeSH
- homologní transplantace škodlivé účinky MeSH
- incidence MeSH
- lidé středního věku MeSH
- lidé MeSH
- mutace MeSH
- neúspěšná terapie MeSH
- pooperační komplikace farmakoterapie etiologie virologie MeSH
- transplantace hematopoetických kmenových buněk škodlivé účinky MeSH
- virová léková rezistence * MeSH
- virová nálož účinky léků MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antivirové látky MeSH
- ganciklovir MeSH
OBJECTIVE: To determine the incidence of infection with ganciclovir-resistant cytomegalovirus (CMV) in adult allogeneic hematopoietic stem cell transplant (HSCT) recipients. Clinical resistance or treatment failure was defined as persistent DNAemia or increasing viral load in peripheral blood after 2 weeks of virostatic treatment. The association between the treatment failure and viral resistance was analysed. The presence of ganciclovir-resistant CMV strains was confirmed by genotypic testing able to detect mutations conferring resistance. METHODS: In 2012 and 2014, 40 patients who underwent allogeneic HSCT for hematologic malignancies and were treated for human CMV reactivation/disease were followed up prospectively. In patients with treatment failure, CMV DNA was isolated and analysed by nucleotide sequence analysis of the UL 97 and UL 54 genes conferring resistance to the virostatic agent. RESULTS: The treatment failure occurred in seven patients, but ganciclovir resistance conferring mutations were only detected in two of them (mutations L595F and M460I in the UL 97 gene). Another mutation in the UL 97 gene (N510S) was found in a patient with recurrent CMV replication who needed to be retreated but did not meet the criteria for treatment failure. CONCLUSION: The low incidence of genetically confirmed ganciclovir-resistant CMV isolates in HSCT recipients with relatively common clinical treatment failure suggests that the mechanism underlying slower viral clearance is often other than mutations conferring ganciclovir resistance to the virus.