Cytomegalovirus (CMV) infection represents one of the main cause mortality after Stem Cell Transplantation. Recently, a protective effect of the T allele of rs12979860 IL28B Single Nucleotide Polymorphisms (SNPs) against CMV infection in the allogenic stem cell transplantation was suggested. We investigate whether the rs12979860 IL28B SNP and the relative rs368234815 (IFN lambda 4) genotype may affect the incidence of active CMV infection in Autologous stem cell transplantation (Auto-SCT) setting. The study included 99 patients who underwent to Auto-SCT. 1L28 and IFN Delta 4 SNPs were correlated with CMV reactivation along with other clinical and treatment parameters. CMV reactivation by CMV DNAemia was evaluated once a week until day 100 from Auto-SCT. CMV reactivation was documented in 50% (TT-Delta G/Delta G), 35% (CC-TT/TT) and 29.2% (CT-TT/Delta G) of the patients respectively. No differences in CMV copies number were recorded at reactivation between different IL28/IFN lambda 4 genotypes. The analysis of patients older than 60 years showed a significantly higher incidence of active CMV infection in the TT-Delta G/Delta G (83%) population with respect to CC-TT/TT (21%) and CT-TT/Delta G (40%) patients. Our data suggest a negative role of TT-Delta G/Delta G genotype in the CMV reactivation in Auto-SCT. The exposure to rituximab and the pre-infusion presence of anti CMV IgG also significantly influenced CMV reactivation.

Annibali, O., Piccioni, L., Tomarchio, V., Circhetta, E., Sarlo, C., Franceschini, L., et al. (2018). Impact of IFN lambda 3/4 single nucleotide polymorphisms on the cytomegalovirus reactivation in autologous stem cell transplant patients. PLOS ONE, 13(7), e0200221 [10.1371/journal.pone.0200221].

Impact of IFN lambda 3/4 single nucleotide polymorphisms on the cytomegalovirus reactivation in autologous stem cell transplant patients

Annibali O.;Sarlo C.;Franceschini L.;Cantonetti M.;Rizzo E.;Riva E.
2018-01-01

Abstract

Cytomegalovirus (CMV) infection represents one of the main cause mortality after Stem Cell Transplantation. Recently, a protective effect of the T allele of rs12979860 IL28B Single Nucleotide Polymorphisms (SNPs) against CMV infection in the allogenic stem cell transplantation was suggested. We investigate whether the rs12979860 IL28B SNP and the relative rs368234815 (IFN lambda 4) genotype may affect the incidence of active CMV infection in Autologous stem cell transplantation (Auto-SCT) setting. The study included 99 patients who underwent to Auto-SCT. 1L28 and IFN Delta 4 SNPs were correlated with CMV reactivation along with other clinical and treatment parameters. CMV reactivation by CMV DNAemia was evaluated once a week until day 100 from Auto-SCT. CMV reactivation was documented in 50% (TT-Delta G/Delta G), 35% (CC-TT/TT) and 29.2% (CT-TT/Delta G) of the patients respectively. No differences in CMV copies number were recorded at reactivation between different IL28/IFN lambda 4 genotypes. The analysis of patients older than 60 years showed a significantly higher incidence of active CMV infection in the TT-Delta G/Delta G (83%) population with respect to CC-TT/TT (21%) and CT-TT/Delta G (40%) patients. Our data suggest a negative role of TT-Delta G/Delta G genotype in the CMV reactivation in Auto-SCT. The exposure to rituximab and the pre-infusion presence of anti CMV IgG also significantly influenced CMV reactivation.
2018
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore MED/15 - MALATTIE DEL SANGUE
English
Adolescent; Adult; Aged; Alleles; Cytomegalovirus; Cytomegalovirus Infections; Female; Genotype; Hematopoietic Stem Cell Transplantation; Humans; Interferons; Interleukins; Lymphoma, Non-Hodgkin; Male; Middle Aged; Multiple Myeloma; Transplantation, Autologous; Virus Activation; Young Adult; Polymorphism, Single Nucleotide
Annibali, O., Piccioni, L., Tomarchio, V., Circhetta, E., Sarlo, C., Franceschini, L., et al. (2018). Impact of IFN lambda 3/4 single nucleotide polymorphisms on the cytomegalovirus reactivation in autologous stem cell transplant patients. PLOS ONE, 13(7), e0200221 [10.1371/journal.pone.0200221].
Annibali, O; Piccioni, L; Tomarchio, V; Circhetta, E; Sarlo, C; Franceschini, L; Cantonetti, M; Rizzo, E; Angeletti, S; Tirindelli, Mc; Scagnolari, C;...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/242778
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