Literature DB >> 30369733

A Low Incidence of Cytomegalo Virus Infection Following Allogeneic Hematopoietic Stem Cell Transplantation Despite a High Seroprevalence.

Anup J Devasia1, Shoba Mammen2, Anu Korula1, Aby Abraham1, N A Fouzia1, Kavitha M Lakshmi1, Asha Mary Abraham2, Alok Srivastava1, Vikram Mathews1, Biju George1.   

Abstract

Cytomegalovirus (CMV) infection remains an important cause of morbidity and mortality following allogeneic stem cell transplantation (SCT). We wanted to study if the high sero-prevalence seen in our population translated into a high incidence of CMV infection following SCT. This is a retrospective analysis of patients who underwent allogeneic SCT between January 2008 and December 2012 at our centre. 475 patients underwent allogeneic SCT for malignant (46.5%) and non-malignant (53.5%) haematological disorders. 463 (97.4%) SCT recipients and 403 (84.8%) SCT donors were IgG seropositive for CMV. CMV reactivation within 100 days post SCT was seen in 174 (36.6%) at a median of 41 days (range 10-100) post SCT. Ganciclovir was used in 166 patients (95.4%) for a mean duration of 16 days (range 5-32). 157 patients (90%) responded to therapy. Sixty-six patients (42.3%) had secondary reactivation of the virus. Use of a male donor (p = 0.000), donor and recipient age > 15 (p = 0.005 and 0.000), unrelated donor (p = 0.000), degree of HLA mismatch (p = 0.000), occurrence of acute GVHD (p = 0.000) and steroid refractory acute GVHD (p = 0.026) were identified as risk factors for CMV reactivation while early neutrophil recovery (< 15 days) was found to be protective (p = 0.004). On multivariate analysis, male donor (p = 0.042), degree of HLA mismatch (p = 0.006), the occurrence of acute GVHD (p = 0.000) and steroid refractory acute GVHD (p = 0.031) continued to remain significant. 5-year overall survival was significantly better in patients without CMV reactivation compared to those who developed reactivation of CMV (68.9 ± 3.7 vs 58.2 ± 4.9% p = 0.004). The incidence of CMV infection does not seem to be higher despite a high sero-prevalence of CMV. However, patients who developed CMV infection post SCT had inferior outcomes.

Entities:  

Keywords:  Cytomegalo virus; Seroprevalence; Stem cell transplantation

Year:  2018        PMID: 30369733      PMCID: PMC6186215          DOI: 10.1007/s12288-018-0960-y

Source DB:  PubMed          Journal:  Indian J Hematol Blood Transfus        ISSN: 0971-4502            Impact factor:   0.900


  27 in total

1.  Seroprevalence of cytomegalovirus among voluntary blood donors in Delhi, India.

Authors:  Atul Kothari; V G Ramachandran; Piyush Gupta; Bharat Singh; Vibha Talwar
Journal:  J Health Popul Nutr       Date:  2002-12       Impact factor: 2.000

2.  Cytomegalovirus reactivation following hematopoietic stem cell transplantation.

Authors:  Sanjeev Kumar Sharma; Suman Kumar; Narendra Agrawal; Lavleen Singh; Anjan Mukherjee; Tulika Seth; Pravas Mishra; Sandeep Mathur; Lalit Dar; Manoranjan Mahapatra
Journal:  J Infect Dev Ctries       Date:  2013-12-15       Impact factor: 0.968

3.  The human cytomegalovirus US11 gene product dislocates MHC class I heavy chains from the endoplasmic reticulum to the cytosol.

Authors:  E J Wiertz; T R Jones; L Sun; M Bogyo; H J Geuze; H L Ploegh
Journal:  Cell       Date:  1996-03-08       Impact factor: 41.582

4.  Influence of donor cytomegalovirus (CMV) status on severity of viral reactivation after allogeneic stem cell transplantation in CMV-seropositive recipients.

Authors:  Floor L Pietersma; Suzanne van Dorp; Monique C Minnema; Jürgen Kuball; Ellen Meijer; Rob Schuurman; Debbie van Baarle
Journal:  Clin Infect Dis       Date:  2011-04-01       Impact factor: 9.079

Review 5.  Cytomegalovirus diseases after hematopoietic stem cell transplantation: a mini-review.

Authors:  Ella J Ariza-Heredia; Lior Nesher; Roy F Chemaly
Journal:  Cancer Lett       Date:  2013-09-13       Impact factor: 8.679

6.  Deficiency of cytomegalovirus (CMV)-specific CD8+ T cells in patients presenting with late-onset CMV disease several years after transplantation.

Authors:  N W Cummins; P J Deziel; R S Abraham; R R Razonable
Journal:  Transpl Infect Dis       Date:  2008-09-21       Impact factor: 2.228

7.  Validation of a DNAemia cutoff for preemptive therapy of cytomegalovirus infection in adult hematopoietic stem cell transplant recipients.

Authors:  G Gerna; D Lilleri; D Caldera; M Furione; L Zenone Bragotti; E P Alessandrino
Journal:  Bone Marrow Transplant       Date:  2008-01-21       Impact factor: 5.483

8.  Risk factors for late cytomegalovirus infection after allogeneic stem cell transplantation using HLA-matched sibling donor: donor lymphocyte infusion and previous history of early CMV infection.

Authors:  D H Kim; J G Kim; N Y Lee; W J Sung; S K Sohn; J S Suh; K S Lee; K B Lee
Journal:  Bone Marrow Transplant       Date:  2004-07       Impact factor: 5.483

Review 9.  CMV-specific T cell therapy.

Authors:  Hermann Einsele; Markus Kapp; Götz Ulrich Grigoleit
Journal:  Blood Cells Mol Dis       Date:  2007-09-11       Impact factor: 3.039

10.  Low-dose short-course intravenous ganciclovir as pre-emptive therapy for CMV viremia post allo-PBSC transplantation.

Authors:  R Vij; H Khoury; R Brown; L T Goodnough; S M Devine; W Blum; D Adkins; J F DiPersio
Journal:  Bone Marrow Transplant       Date:  2003-10       Impact factor: 5.483

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  1 in total

1.  Cytomegalovirus infection may be oncoprotective against neoplasms of B-lymphocyte lineage: single-institution experience and survey of global evidence.

Authors:  Marko Janković; Aleksandra Knežević; Milena Todorović; Irena Đunić; Biljana Mihaljević; Ivan Soldatović; Jelena Protić; Nevenka Miković; Vera Stoiljković; Tanja Jovanović
Journal:  Virol J       Date:  2022-09-29       Impact factor: 5.913

  1 in total

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