A linked donor-recipient study to evaluate parvovirus B19 transmission by blood component transfusion.

Pubmed ID: 19687508

Pubmed Central ID: PMC2766683

Journal: Blood

Publication Date: Oct. 22, 2009

Affiliation: Westat Inc, Rockville, MD, USA. skleinman@shaw.ca

MeSH Terms: Humans, Aged, Case-Control Studies, Middle Aged, Blood Component Transfusion, Blood Donors, DNA, DNA, Viral, Mass Screening, Parvoviridae Infections, Parvovirus B19, Human, Polymerase Chain Reaction, Viremia

Grants: N01-HB-47175, N01-HB-57181, N01HB47175, N01HB57181

Authors: Busch MP, Busch MP, Busch MP, Kleinman SH, Glynn SA, Lee TH, Tobler LH, Schlumpf KS, Todd DS, Qiao H, Yu MY, Cable R, Rios J, Benjamin R, Hillyer CD, Hillyer KL, Roback JD, Gottschall J, Mast AE, Sacher RA, Wilkinson SL, Carey PM, Murphy EL, Custer B, Triulzi D, Kakaiya R, Kiss J, Norris P, Schulman J, King M, Nemo GJ, Glynn S, Dodd RY, Nass CC, Ness P, Higgins M, Garratty G, Hutching S, Hirose T, LeParc G, Gilcher RO, Smith JW, Juengal R, Irwin D, Viele M, Toy P, Schreiber GB, Zuck TE

Cite As: Kleinman SH, Glynn SA, Lee TH, Tobler LH, Schlumpf KS, Todd DS, Qiao H, Yu MY, Busch MP, National Heart Lung and Blood Institute Retrovirus Epidemiology Donor Study-II (NHLBI REDS-II). A linked donor-recipient study to evaluate parvovirus B19 transmission by blood component transfusion. Blood 2009 Oct 22;114(17):3677-83. Epub 2009 Aug 17.

Studies:

Abstract

Parvovirus B19V infection can be a serious infection for hematology patients with underlying hemolysis or compromised erythropoiesis syndromes. Although case reports of B19V transmission by blood component transfusion (as contrasted to manufactured plasma derivatives) are rare, no studies have systematically determined a rate of transmission to recipients transfused with B19V DNA-positive components. We used a linked donor and recipient repository and a sensitive, quantitative B19V DNA polymerase chain reaction (PCR) assay to assess such transmission in B19V-susceptible (ie, anti-B19V immunoglobulin G [IgG] negative) recipients. We assessed 112 B19V DNA-positive components from 105 donors (of 12 529 tested donations) transfused into a population of surgical patients with a pretransfusion B19V IgG seroprevalence of 78%. We found no transmission to 24 susceptible recipients from transfusion of components with B19V DNA at concentrations less than 10(6) IU/mL (upper 95% confidence interval, 11.7%). We found an anamnestic IgG response in one pretransfusion seropositive recipient transfused with a component containing greater than 10(10) IU/mL B19V DNA. These findings show either that transmission from components with less than 10(6) IU/mL does not occur, or, if it does, it is an uncommon event. These data do not support the need to routinely screen blood donations with a sensitive B19V DNA nucleic acid assay.