Ganciclovir treatment failure in adult allogeneic hematopoietic stem cell transplant recipients with cytomegalovirus infection - a single centre experience

被引:0
|
作者
Vejrazkova, E. [1 ]
Hubacek, P. [2 ,3 ,4 ]
Kutova, R. [5 ,6 ]
Pliskova, L. [5 ,6 ]
Kostal, M. [1 ]
Stepanova, V [6 ,7 ]
Zavrelova, A. [1 ]
Radocha, J. [1 ]
Mala, E. [6 ,8 ]
Zak, P. [1 ]
机构
[1] Hradci Kralove Univ Karlovy, Hradci Kralove & Lekarska Fak, Fak Nemocnice, Interni Hematol Klin 4, Prague, Czech Republic
[2] Univ Karlovy, Fak Nemocnice Motole, Klin Detske Hematol & Onkol, Prague, Czech Republic
[3] Univ Karlovy, Fak Nemocnice Motole, Ustav Lekarske Mikrobiol, Prague, Czech Republic
[4] Univ Karlovy, Lekarska Fak 2, Prague, Czech Republic
[5] Hradci Kralove Univ Karlovy, Fak Nemocnice Hradci Kralove, Ustav Klin Biochem & Diagnost, Prague, Czech Republic
[6] Hradci Kralove Univ Karlovy, Lekarska Fak, Prague, Czech Republic
[7] Hradci Kralove Univ Karlovy, Fak Nemocnice Hradci Kralove, Ustav Klin Mikrobiol, Prague, Czech Republic
[8] Hradci Kralove Univ Karlovy, Fak Nemocnice Hradci Kralove, Ustav Klin Imunol & Alergol, Prague, Czech Republic
来源
关键词
human cytomegalovirus; ganciclovir; valganciclovir viral; resistance; hematopoietic stem cell transplantation; UL97 PHOSPHOTRANSFERASE MUTATIONS; DRUG-RESISTANT CYTOMEGALOVIRUS; ANTIVIRAL RESISTANCE; THERAPY; EMERGENCE; DISEASE; LOAD; CMV;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
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页码:160 / 168
页数:9
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