Characterization of Markers of the Progression of Human Parvovirus B19 Infection in Virus DNA-Positive Plasma Samples

被引:6
作者
Bonjoch, Xavier [1 ]
Obispo, Francesc [1 ]
Alemany, Cristina [1 ]
Pacha, Ana [1 ]
Rodriguez, Esteban [1 ]
Xairo, Dolors [1 ]
机构
[1] Biomat SA, Grifols, Div Anal, Barcelona 08150, Spain
关键词
Antibodies; Blood safety; Donation deferral period; Immune response; Parvovirus B19; Plasma donation; Transfusion-associated infections; POLYMERASE-CHAIN-REACTION; HUMAN ERYTHROVIRUS B19; SICKLE-CELL-DISEASE; DRY-HEAT-TREATMENT; RED-BLOOD-CELLS; REAL-TIME PCR; NONENVELOPED VIRUSES; DONORS; PREVALENCE; VIREMIA;
D O I
10.1159/000381979
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Accurate characterization of the infection stage in parvovirus B19(B19V)-positive plasma donations would help establish the donation deferral period to contribute to a safe fractionation pool of plasma. Methods: Viral DNA load of 74 B19V DNA-positive plasma samples from whole blood donations was determined by titration using nucleic acid testing. Markers of cellular (neopterin) and humoral (B19V-specific IgM and IgG) immune response were determined by ELISA in 32 B19V DNA-positive samples and in 13 B19V DNA-negative samples. The infection progression profile was estimated according to B19V DNA load and the presence of immune response markers. Results: B19V DNA load in the 74 samples was 10(6)-10(13) IU/ml. The distribution of 14 out of 32 selected B19V DNA-positive samples plus 2 B19V DNA-negative samples with no immune response marker followed along an upward curve according to B19V DNA load. After the peak, the distribution of 18 immune marker-positive samples followed along a downward curve according to their B19V DNA load and was grouped as follows: neopterin In = 4), neopterin+ IgM (n = 8), neopterin + IgM + IgG In = 3), IgM + IgG (n = 2), IgM (n = 1). There were 11 B19V DNA-negative IgG-positive samples. Conclusion: This study of B19V-DNA load and levels of neopterin, IgM, and IgG allows for reliable characterization and distribution into the different stages of B19V infection. (C) 2015 S. Karger GmbH, Freiburg
引用
收藏
页码:233 / 238
页数:8
相关论文
共 48 条
[1]   Collaborative study to establish a World Health Organization International genotype panel for parvovirus B19 DNA nucleic acid amplification technology (NAT)-based assays [J].
Baylis, S. A. ;
Ma, L. ;
Padley, D. J. ;
Heath, A. B. ;
Yu, M. W. .
VOX SANGUINIS, 2012, 102 (03) :204-211
[2]   Evaluation of different assays for the detection of parvovirus B19 DNA in human plasma [J].
Baylis, SA ;
Shah, N ;
Minor, PD .
JOURNAL OF VIROLOGICAL METHODS, 2004, 121 (01) :7-16
[3]   Kinetics of inactivating human parvovirus B19 and porcine parvovirus by dry-heat treatment [J].
Bluemel, Johannes ;
Stuehler, Albert ;
Dichtelmueller, Herbert .
TRANSFUSION, 2008, 48 (04) :790-791
[4]   Inactivation of parvovirus B19 during pasteurization of human serum albumin [J].
Blümel, J ;
Schmidt, I ;
Willkommen, H ;
Löwer, J .
TRANSFUSION, 2002, 42 (08) :1011-1018
[5]   False-negative serology in patients with acute parvovirus B19 infection [J].
Bredl, Simon ;
Plentz, Annelie ;
Wenzel, Juergen J. ;
Pfister, Heiko ;
Moest, Johannes ;
Modrow, Susanne .
JOURNAL OF CLINICAL VIROLOGY, 2011, 51 (02) :115-120
[6]   Antibody-mediated opsonization of red blood cells in parvovirus B19 infection [J].
Chehadeh, Wassim ;
Halim, Medhat A. ;
Al-Nakib, Widad .
VIROLOGY, 2009, 390 (01) :56-63
[7]   Multiplex real-time PCR for the detection and quantification of latent and persistent viral genomes in cellular or plasma blood fractions [J].
Compston, Lara Isobel ;
Sarkobie, Francis ;
Li, Chengyao ;
Candotti, Daniel ;
Opare-Sem, Ohene ;
Allain, Jean-Pierre .
JOURNAL OF VIROLOGICAL METHODS, 2008, 151 (01) :47-54
[8]   Advances in the biology, diagnosis and host-pathogen interactions of parvovirus B19 [J].
Corcoran, A ;
Doyle, S .
JOURNAL OF MEDICAL MICROBIOLOGY, 2004, 53 (06) :459-475
[9]  
Council of Europe Human Plasma (Pooled and Treated for Virus Inactivation), 2006, COUNC EUR HUM PLASM
[10]   Prolonged parvovirus B19 viremia in spite of neutralizing antibodies after erythema infectiosum in pregnancy [J].
Dobec, Marinko ;
Juchler, Antoinette ;
Flaviano, Alois ;
Kaeppeli, Franz .
GYNECOLOGIC AND OBSTETRIC INVESTIGATION, 2007, 63 (01) :53-54