| Literature DB >> 29753162 |
María Suárez-Lledó1, Núria Martínez-Cibrián2, Gonzalo Gutiérrez-García2, Veselka Dimova-Svetoslavova3, Ma Angeles Marcos3, Beatriz Martín-Antonio4, Alejandra Martínez-Trillos2, Neus Villamor5, Laura Rosiñol6, Carmen Martínez7, Francesc Fernández-Avilés7, Carolina García-Vidal8, Álvaro Urbano-Ispizua7, Montserrat Rovira7.
Abstract
This study examined the impact of prednisone (PDN) on cytomegalovirus (CMV) infection after allogeneic stem cell transplantation (allo-SCT) according to donor and recipient CMV serostatus. Seventy-five patients underwent allo-SCT from June 2010 to July 2012. The risk of CMV infection according to donor and recipient serostatus was defined as follows: high risk (HR; D-/R+), intermediate risk (IR; D+/R+ and D+/R-), and low risk (D-/R-). Forty-five patients (60%) developed CMV infection, and 46 patients (61%) received steroids (PDN ≥ 1 mg/kg/day) to treat acute graft-versus-host disease. CMV infection was more common in those treated with steroids than in those not treated with steroids (70% versus 44%, respectively, P < .05). Overall, 40% of patients had recurrent CMV infection (50% PDN versus 24% no PDN, P < .05). Steroids had no impact on the incidence of CMV infection or its recurrence in HR patients; however, steroids did prolong the need for antiviral treatment. The incidence of CMV infection in IR patients was higher in those receiving PDN (80% PDN versus 41% no PDN, P = .01); recurrence rates were also higher (55% PDN versus 18% no PDN, P = .02). We analyzed CMV-specific immune reconstitution in the first 22 patients of the series and observed that patients on steroids had lower levels of CMV-specific lymphocytes TCD8 (P < .05 on days +60, +100, and +180) and that CMV-specific immune reconstitution (defined as lymphocytes CD8/IFN ≥ 1 cell/µL) was achieved later (after day +100 post-SCT) in the steroid group.Entities:
Keywords: Allo-SCT; CMV Serology; CMV infection; CMV-specific immune response; Steroids
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Year: 2018 PMID: 29753162 DOI: 10.1016/j.bbmt.2018.05.001
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742