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Erschienen in: Journal of Clinical Immunology 6/2010

01.11.2010

Prospective Evaluation of Epstein–Barr Virus Reactivation After Stem Cell Transplantation: Association with Monoclonal Gammopathy

verfasst von: Patrizia Chiusolo, Elisabetta Metafuni, Paola Cattani, Nicola Piccirillo, Rosaria Santangelo, Stefania Manzara, Silvia Bellesi, Teresa De Michele, Giuseppe Leone, Simona Sica

Erschienen in: Journal of Clinical Immunology | Ausgabe 6/2010

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Abstract

Epstein–Barr Virus (EBV) reactivation and EBV-related post-transplant lymphoproliferative disease (PTLD) have emerged as a severe complication after stem cell transplantation (SCT). We prospectively evaluated 104 consecutive patients receiving SCT either autologous or allogeneic. Fifty-two patients (50%) presented EBV DNA-emia and five of them developed PTLD proven or probable. PTLD rate was 9.6% among patients with EBV DNA-emia. One patient developed PTLD without EBV DNA-emia (0.96%). Overall PTLD incidence was 5.7%. No PTLD developed after autologous SCT. EBV DNA-emia was significantly more frequent after allogeneic than autologous SCT (60.7% vs 17.4%, p = 0.0002). At EBV reactivation, serum protein electrophoresis and immunofixation were assessed. Global incidence of γ-peak after allogeneic SCT with EBV reactivation was 65.3% (32/49 patients) and monoclonal gammopathy (MG) was identified in 23/28 evaluable patients (82%). All patients with PTLD developed γ-peak and in five of them MG was identified. MG is consistently associated with EBV DNA-emia and may help identification of progression to PTLD after allogeneic SCT.
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Metadaten
Titel
Prospective Evaluation of Epstein–Barr Virus Reactivation After Stem Cell Transplantation: Association with Monoclonal Gammopathy
verfasst von
Patrizia Chiusolo
Elisabetta Metafuni
Paola Cattani
Nicola Piccirillo
Rosaria Santangelo
Stefania Manzara
Silvia Bellesi
Teresa De Michele
Giuseppe Leone
Simona Sica
Publikationsdatum
01.11.2010
Verlag
Springer US
Erschienen in
Journal of Clinical Immunology / Ausgabe 6/2010
Print ISSN: 0271-9142
Elektronische ISSN: 1573-2592
DOI
https://doi.org/10.1007/s10875-010-9454-x

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