CHRONIC ANEMIA DUE TO PARVOVIRUS B19 INFECTION IN A BONE-MARROW TRANSPLANT PATIENT AFTER PLATELET TRANSFUSION

Citation
Bj. Cohen et al., CHRONIC ANEMIA DUE TO PARVOVIRUS B19 INFECTION IN A BONE-MARROW TRANSPLANT PATIENT AFTER PLATELET TRANSFUSION, Transfusion, 37(9), 1997, pp. 947-952
Citations number
26
Categorie Soggetti
Hematology
Journal title
ISSN journal
00411132
Volume
37
Issue
9
Year of publication
1997
Pages
947 - 952
Database
ISI
SICI code
0041-1132(1997)37:9<947:CADTPB>2.0.ZU;2-S
Abstract
BACKGROUND: Many reports document the transmission of human parvovirus B19 (B19) infection by clotting factor concentrates manufactured from large plasma pools. Transmission via other blood components originati ng from a single donor or a small number of donors, however, seems to occur only rarely. The study reported here identifies a B19 infection that was transmitted via a platelet donation. CASE REPORT: A multiply transfused allogeneic bone marrow transplant patient developed chronic anemia due to persistent B19 infection. The anemia responded to thera py with intravenous immunoglobulin. It was postulated that a transfusi on was the source of the B19 infection. Archived sera from 90 implicat ed blood donors were tested for B19 IgM and DNA by the use of dot-blot hybridization and a nested polymerase chain reaction with primers fro m the B19 nonstructural gene. B19 DNA from patient and donor sera were sequenced. One of the 90 blood donors (Donor A) was B19 IgM positive and had a high level of B19 DNA. The patient was viremic 3 days after transfusion of platelets from this donor, and the sequence of B19 DNA from the patient exactly matched that of B19 DNA from the donor. A sec ond blood donor (Donor B) had a low level of B19 DNA but was IgM negat ive. The patient showed no evidence of B19 infection after the transfu sion of red cells from Donor B, and the sequence of this donor's B19 D NA was different from that in the patient. CONCLUSION: Blood Donor A w ith asymptomatic acute B19 infection was the source of B19 infection i n the bone marrow transplant patient. Donor B with a low level of B19 DNA was not the source of infection.