Predictive Value of Quantitative PCR-Based Viral Burden Analysis for Eight Human Herpesviruses in Pediatric Solid Organ Transplant Patients  Xin Bai,

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Predictive Value of Quantitative PCR-Based Viral Burden Analysis for Eight Human Herpesviruses in Pediatric Solid Organ Transplant Patients  Xin Bai, Beverly Barton Rogers, Paul C. Harkins, John Sommerauer, Robert Squires, Kathleen Rotondo, Albert Quan, D. Brian Dawson, Richard H. Scheuermann  The Journal of Molecular Diagnostics  Volume 2, Issue 4, Pages 191-201 (November 2000) DOI: 10.1016/S1525-1578(10)60637-X Copyright © 2000 American Society for Investigative Pathology and Association for Molecular Pathology Terms and Conditions

Figure 1 Quantitative ICS-PCR analysis of eight human herpesviruses in patient samples. PCR reactions containing purified DNA derived from 10 μl whole blood and 20 molecules of the HHVQ-1 ICS standard were amplified as described in Materials and Methods. DNA isolated from three different patients (A, B, and C) was amplified with primers specific for HSV-1 (lanes 2), HSV-2 (lanes 3), VZV (lanes 4), EBV (lanes 5), CMV (lanes 6), HHV-6 (lanes 7), HHV-7 (lanes 8), and KSHV (lanes 9). The sizes of the predicted PCR products derived from the HHVQ-1 standard and the specific viruses are given inTable 1. PCR products derived from the HHVQ-1 ICS using the virus-specific primers are bracketed as standard bands.Arrowheads indicate PCR products derived from the viral targets. The weak bands observed with the HSV-2 primers in Aand C, lanes 3 are nonspecific. D: DNA from the patient analyzed in C was re-analyzed by amplification with CMV-specific PCR primers and the amount of whole blood DNA indicated. In each panel, lane 1 contains a 123-bp DNA ladder as a size marker; the 123-bp fragment is indicated with an asterisk. The Journal of Molecular Diagnostics 2000 2, 191-201DOI: (10.1016/S1525-1578(10)60637-X) Copyright © 2000 American Society for Investigative Pathology and Association for Molecular Pathology Terms and Conditions

Figure 2 Quantification of herpesvirus targets by ICS-PCR in a reference pediatric population. The levels of eight human herpesviruses in the blood of 51 pediatric emergency room patients was determined by ICS-PCR as described in Figure 1. The diamonds indicate values (in VT/ml blood) for all samples that gave detectable virus-specific bands. The proportion of samples that gave detectable bands is indicated above each virus designation. Green diamonds are values from the subset of patients presenting with fever in this group. The red triangles indicate the average limits of detection for each virus in all negative samples analyzed in this study. The Journal of Molecular Diagnostics 2000 2, 191-201DOI: (10.1016/S1525-1578(10)60637-X) Copyright © 2000 American Society for Investigative Pathology and Association for Molecular Pathology Terms and Conditions

Figure 3 Quantification of herpesvirus targets by ICS-PCR in pediatric solid organ transplant patients. The levels of eight human herpesviruses in 264 blood samples from 27 pediatric solid organ transplant recipients was determined by ICS-PCR as described in Figure 1. The diamonds indicate values (in VT/ml blood) for all samples that gave detectable virus-specific bands. The proportion of samples and patients with positive results for each virus can be found in Table 2. The green diamonds indicate the levels in samples from patients with clinical or laboratory evidence of an acute viral infection within 5 weeks of the date of sample harvest (see text for details). The red trianglesindicate the average limits of detection for each virus in all negative samples analyzed in this study. The Journal of Molecular Diagnostics 2000 2, 191-201DOI: (10.1016/S1525-1578(10)60637-X) Copyright © 2000 American Society for Investigative Pathology and Association for Molecular Pathology Terms and Conditions

Figure 4 CMV levels in sequential samples from selected patients with evidence of acute infection. CMV levels were determined by ICS-PCR in multiple samples from three patients who developed clinical disease apparently associated with an acute CMV infection. Evidence for CMV infection included changes in CMV serology, histological detection of CMV inclusions, or other evidence of tissue damage. CMV levels are plotted against the time the sample was harvested after organ transplantation.Open symbols indicate samples in which no viral band was detected; the viral burdens indicated represent the limits of detection for that PCR reaction. The significant clinical findings are as follows. A: Patient 1. a: High creatinine levels were noted during routine laboratory studies. b: Cells containing viral inclusion bodies were identified in kidney biopsies leading to a diagnosis of CMV nephritis. Retinitis was also detected by clinical examination. The levels of cyclosporin were lowered; mycophenolate treatment was discontinued; treatment with ganciclovir and cytogam was begun. B: Patient 6. c: Elevated liver enzymes were noted during retrospective chart review. d: Cyclosporin and prednisone levels were reduced. e: Acyclovir treatment was begun. C:Patient 7. f: Patient was admitted to the hospital with complaint of recurrent fever. CMV serology was positive in the patient that was previously negative. Lymphopenia was noted. Patient was switched from acyclovir to ganciclovir and cytogam. Mycophenolate treatment was discontinued. g: Evidence of acute cellular rejection (tubulitis) from kidney biopsy was noted. Patient was treated with mycophenolate. The Journal of Molecular Diagnostics 2000 2, 191-201DOI: (10.1016/S1525-1578(10)60637-X) Copyright © 2000 American Society for Investigative Pathology and Association for Molecular Pathology Terms and Conditions

Figure 5 Clinical correlations in selected patients with high EBV levels. EBV levels were determined by ICS-PCR in samples from two representative patients that showed relatively high EBV levels. EBV levels are plotted against the time the sample was harvested after organ transplantation.Open symbol indicates sample in which no viral band was detected; viral burden represents the limits of detection for that PCR reaction. The significant clinical findings are as follows.A: Patient 17. a: Cyclosporin levels were increased. b: Mild gastrointestinal symptoms developed; the patient was treated with intravenous prednisone. c: Mild lymphadenopathy was noted on chest X-ray. Treatment with ganciclovir and cytogam was begun. Immunosuppression was reduced slightly. d: Patient presented with gastroenteritis. e, f: CT scans show increasing lymph node size and number. B: Patient 5. g: Patient was admitted to hospital with complaints of nausea, vomiting, and diarrhea. h: Patient was admitted to hospital with pneumonia. Elevated liver enzymes were noted. High EBV and CMV IgG were detected by serological evaluation. i: Immunosuppression was tapered down threefold. The Journal of Molecular Diagnostics 2000 2, 191-201DOI: (10.1016/S1525-1578(10)60637-X) Copyright © 2000 American Society for Investigative Pathology and Association for Molecular Pathology Terms and Conditions