Cytomegalovirus infectivity in whole blood following leukocyte reduction by filtration
- PMID: 11447751
- DOI: 10.1309/PVFR-DDWE-302T-WFA1
Cytomegalovirus infectivity in whole blood following leukocyte reduction by filtration
Abstract
Cytomegalovirus (CMV) may be transmitted by transfusion of whole blood and cellular components processed according to standard processing procedures. A need exists to develop new procedures to remove CMV and other leukocyte-borne viruses from donor blood. Ten patients (AIDS/bone marrow transplants) who were CMV antigenemic (virus subsequently confirmed by isolation), donated 50 mL of venous blood within 24 to 72 hours of the initial antigen detection. Twenty-five-milliliter aliquots of each specimen were passed through Purecell Neo Neonatal Leukocyte Reduction Filters (Pall, East Hills, NY). The remaining 25-mL nonfiltered aliquots, as well as the blood filtrates, were subjected to infectivity endpoint determinations. The Purecell Neo filter effected a 3 to 4 log10 leukocyte reduction. CMV input titers ranged from less than 10 to 7.3 x 10(1) median tissue culture infectious dose (TCID50) per milliliter. CMV was not isolated from any postfiltration effluent (i.e., leukocytes, erythrocytes, or plasma). CMV DNA was not detected by nested polymerase chain reaction in 8 of 10 postfiltrate blood specimens. The Purecell Neo filter was efficacious in eliminating or significantly reducing viral (CMV) load in venous blood.
Similar articles
-
High prevalence of cytomegalovirus DNA in plasma samples of blood donors in connection with seroconversion.Transfusion. 2007 Nov;47(11):1972-83. doi: 10.1111/j.1537-2995.2007.01420.x. Transfusion. 2007. PMID: 17958525
-
Transfusion-transmitted cytomegalovirus: behaviour of cell-free virus during blood component processing. A study on the safety of labile blood components in Switzerland.Blood Transfus. 2020 Nov;18(6):446-453. doi: 10.2450/2020.0241-19. Epub 2020 Feb 28. Blood Transfus. 2020. PMID: 32203012 Free PMC article.
-
Once daily ganciclovir as initial pre-emptive therapy delayed until threshold CMV load > or =10000 copies/ml: a safe and effective strategy for allogeneic stem cell transplant patients.Bone Marrow Transplant. 2006 Jan;37(1):51-6. doi: 10.1038/sj.bmt.1705213. Bone Marrow Transplant. 2006. PMID: 16284613
-
Transfusion-transmitted cytomegalovirus infection.Hematol Oncol Clin North Am. 1995 Feb;9(1):155-66. Hematol Oncol Clin North Am. 1995. PMID: 7737939 Review.
-
[Leukocyte depletion and infection by cytomegalovirus].Transfus Clin Biol. 2000 Jun;7 Suppl 1:31s-35s. doi: 10.1016/s1246-7820(00)80013-0. Transfus Clin Biol. 2000. PMID: 10919221 Review. French.
Cited by
-
Determination of the Biological Form of Human Cytomegalovirus DNA in the Plasma of Solid-Organ Transplant Recipients.J Infect Dis. 2017 Apr 1;215(7):1094-1101. doi: 10.1093/infdis/jix069. J Infect Dis. 2017. PMID: 28407149 Free PMC article.
-
Pathogen at the Gates: Human Cytomegalovirus Entry and Cell Tropism.Viruses. 2018 Dec 11;10(12):704. doi: 10.3390/v10120704. Viruses. 2018. PMID: 30544948 Free PMC article. Review.
-
Large-Scale Screening of HCMV-Seropositive Blood Donors Indicates that HCMV Effectively Escapes from Antibodies by Cell-Associated Spread.Viruses. 2018 Sep 14;10(9):500. doi: 10.3390/v10090500. Viruses. 2018. PMID: 30223489 Free PMC article.
-
Virion Glycoprotein-Mediated Immune Evasion by Human Cytomegalovirus: a Sticky Virus Makes a Slick Getaway.Microbiol Mol Biol Rev. 2016 Jun 15;80(3):663-77. doi: 10.1128/MMBR.00018-16. Print 2016 Sep. Microbiol Mol Biol Rev. 2016. PMID: 27307580 Free PMC article. Review.
-
HCMV modulation of cellular PI3K/AKT/mTOR signaling: New opportunities for therapeutic intervention?Antiviral Res. 2019 Mar;163:82-90. doi: 10.1016/j.antiviral.2019.01.009. Epub 2019 Jan 19. Antiviral Res. 2019. PMID: 30668978 Free PMC article. Review.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical