Using Epstein-Barr Viral Load Assays To Diagnose, Monitor, and Prevent Posttransplant Lymphoproliferative Disorder
Top Cited Papers
Open Access
- 1 April 2010
- journal article
- review article
- Published by American Society for Microbiology in Clinical Microbiology Reviews
- Vol. 23 (2) , 350-366
- https://doi.org/10.1128/cmr.00006-09
Abstract
Summary: Epstein-Barr virus (EBV) DNA measurement is being incorporated into routine medical practice to help diagnose, monitor, and predict posttransplant lymphoproliferative disorder (PTLD) in immunocompromised graft recipients. PTLD is an aggressive neoplasm that almost always harbors EBV DNA within the neoplastic lymphocytes, and it is often fatal if not recognized and treated promptly. Validated protocols, commercial reagents, and automated instruments facilitate implementation of EBV load assays by real-time PCR. When applied to either whole blood or plasma, EBV DNA levels reflect clinical status with respect to EBV-related neoplasia. While many healthy transplant recipients have low viral loads, high EBV loads are strongly associated with current or impending PTLD. Complementary laboratory assays as well as histopathologic examination of lesional tissue help in interpreting modest elevations in viral load. Circulating EBV levels in serial samples reflect changes in tumor burden and represent an effective, noninvasive tool for monitoring the efficacy of therapy. In high-risk patients, serial testing permits early clinical intervention to prevent progression toward frank PTLD. Restoring T cell immunity against EBV is a major strategy for overcoming PTLD, and novel EBV-directed therapies are being explored to thwart virus-driven neoplasia.Keywords
This publication has 205 references indexed in Scilit:
- The Impact of EBV Load on T-Cell Immunity in Pediatric Thoracic Transplant RecipientsTransplantation, 2009
- Epstein–Barr virus LMP2A accelerates MYC-induced lymphomagenesisOncogene, 2009
- Tumor-derived Variants of Epstein-Barr Virus Latent Membrane Protein 1 Induce Sustained Erk Activation and c-FosJournal of Biological Chemistry, 2008
- High levels of Epstein–Barr virus DNA in latently infected gastric adenocarcinomaLaboratory Investigation, 2008
- Current understanding of the role of Epstein–Barr virus in lymphomagenesis and therapeutic approaches to EBV-associated lymphomasLeukemia & Lymphoma, 2008
- Epstein–Barr virus nuclear protein EBNA3C is required for cell cycle progression and growth maintenance of lymphoblastoid cellsProceedings of the National Academy of Sciences, 2006
- Validation of Roche LightCycler Epstein-Barr Virus Quantification Reagents in a Clinical Laboratory SettingThe Journal of Molecular Diagnostics, 2006
- A phase 1/2 trial of arginine butyrate and ganciclovir in patients with Epstein-Barr virus–associated lymphoid malignanciesBlood, 2006
- Treatment of solid organ transplant recipients with autologous Epstein Barr virus–specific cytotoxic T lymphocytes (CTLs)Blood, 2006
- LMP1 Strain Variants: Biological and Molecular PropertiesJournal of Virology, 2006