Monitoring human cytomegalovirus infection in pediatric hematopoietic stem cell transplant recipients: using an affordable in‐house qPCR assay for management of HCMV infection under limited resources. (6th March 2015)

• Record Type: Journal Article
• Authors: Khansarinejad, Behzad; Soleimanjahi, Hoorieh; Mirab Samiee, Siamak; Hamidieh, Amir Ali; Paryan, Mahdi; Sanahmadi, Yadollah; Karami, Manoochehr; Mondanizadeh, Mahdieh
• Is Part Of: Transplant international. Volume 28:Number 5(2015:May)
• Page Start: 594
• Page End: 603
• Publication Date: 2015-03-06
• Subjects: antigenemia -- cytomegalovirus -- pediatric -- pp65 -- qPCR -- transplantation; Transplantation of organs, tissues, etc -- Periodicals; 617.95405
• DOI: 10.1111/tri.12545
• Languages: English
• ISSNs: 0934-0874

Abstract

Summary: Quantitative real‐time PCR (qPCR) assay is accepted as the method of choice for monitoring human cytomegalovirus (HCMV) infection in hematopoietic stem cell transplant recipients, but the high cost of commercial kits has hampered its use in many developing countries. In this study, an affordable in‐house qPCR was used to manage HCMV infection in pediatric patients and the diagnostic value of this method was compared with the conventional pp65 antigenemia assay. A total number of 1179 samples from 82 recipients were used in this study, and the effect of some potential risk factors on HCMV reactivation was evaluated. The qPCR was able to detect HCMV reactivation earlier and with higher sensitivity than antigenemia assay. Forty‐six episodes of reactivation were detected in 39 patients, of which all were detected by the qPCR assay, while only 21 episodes were diagnosed by antigenemia. The DNAemia level of 1284 IU/ml plasma was defined as the optimal cutoff value for starting pre‐emptive therapy. It was shown that the acute GVHD severity and the relationship of donor and recipient are the most significant risk factors for HCMV reactivation. The data suggest that the antigenemia method for monitoring HCMV reactivation could be substituted by the qPCR assay.