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Emerging Infectious Diseases That Threaten the Blood Supply

Following the devastating effects of blood-transmitted human immunodeficiency virus (HIV), blood establishments have become increasingly vigilant for the emergence or re-emergence of new threats to the safety of the blood supply. Many agents have fulfilled the broad definition of emerging blood-tran...

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Autores principales: Alter, Harvey J., Stramer, Susan L., Dodd, Roger Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118992/
https://www.ncbi.nlm.nih.gov/pubmed/17198845
http://dx.doi.org/10.1053/j.seminhematol.2006.09.016
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author Alter, Harvey J.
Stramer, Susan L.
Dodd, Roger Y.
author_facet Alter, Harvey J.
Stramer, Susan L.
Dodd, Roger Y.
author_sort Alter, Harvey J.
collection PubMed
description Following the devastating effects of blood-transmitted human immunodeficiency virus (HIV), blood establishments have become increasingly vigilant for the emergence or re-emergence of new threats to the safety of the blood supply. Many agents have fulfilled the broad definition of emerging blood-transmitted infections, including West Nile virus (WNV), Trypanosoma cruzi, Plasmodium spp., Babesia spp., parvovirus B19, dengue virus, and the prions that cause variant Creutzfeld-Jacob disease (vCJD). Other agents such as human herpes virus- 8 (HHV-8—Kaposi’s sarcoma virus) and Borellia (Lyme disease) and, perhaps, avian flu virus, are known to have a viremic phase, but have not yet been proved to be transfusion-transmitted. In the wake of these threats, transfusion services use a variety of donor screening interventions, including serologic assays, nucleic acid assays, and geographic exclusions based on potential exposure. The ultimate safeguard may be a pre-emptive pathogen inactivation strategy that will disrupt all nucleic acid–containing agents (though not prions). Considerable effort and resources have been invested in this arena, but currently no single technique is effective for inactivation of both liquid and cellular blood products and toxicity issues have not been completely resolved. The blood supply is remarkably safe with the risk of major pathogens such as hepatitis C virus (HCV) and HIV now reduced to less than one transmission per 2 to 3 million exposures. However, to approach near-zero infectious disease risk for emerging and re-emerging pathogens, new strategies such as pathogen inactivation or multi-pathogen microarray technology will need to be developed or refined.
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spelling pubmed-71189922020-04-03 Emerging Infectious Diseases That Threaten the Blood Supply Alter, Harvey J. Stramer, Susan L. Dodd, Roger Y. Semin Hematol Article Following the devastating effects of blood-transmitted human immunodeficiency virus (HIV), blood establishments have become increasingly vigilant for the emergence or re-emergence of new threats to the safety of the blood supply. Many agents have fulfilled the broad definition of emerging blood-transmitted infections, including West Nile virus (WNV), Trypanosoma cruzi, Plasmodium spp., Babesia spp., parvovirus B19, dengue virus, and the prions that cause variant Creutzfeld-Jacob disease (vCJD). Other agents such as human herpes virus- 8 (HHV-8—Kaposi’s sarcoma virus) and Borellia (Lyme disease) and, perhaps, avian flu virus, are known to have a viremic phase, but have not yet been proved to be transfusion-transmitted. In the wake of these threats, transfusion services use a variety of donor screening interventions, including serologic assays, nucleic acid assays, and geographic exclusions based on potential exposure. The ultimate safeguard may be a pre-emptive pathogen inactivation strategy that will disrupt all nucleic acid–containing agents (though not prions). Considerable effort and resources have been invested in this arena, but currently no single technique is effective for inactivation of both liquid and cellular blood products and toxicity issues have not been completely resolved. The blood supply is remarkably safe with the risk of major pathogens such as hepatitis C virus (HCV) and HIV now reduced to less than one transmission per 2 to 3 million exposures. However, to approach near-zero infectious disease risk for emerging and re-emerging pathogens, new strategies such as pathogen inactivation or multi-pathogen microarray technology will need to be developed or refined. Elsevier Inc. 2007-01 2006-12-30 /pmc/articles/PMC7118992/ /pubmed/17198845 http://dx.doi.org/10.1053/j.seminhematol.2006.09.016 Text en Copyright © 2007 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Alter, Harvey J.
Stramer, Susan L.
Dodd, Roger Y.
Emerging Infectious Diseases That Threaten the Blood Supply
title Emerging Infectious Diseases That Threaten the Blood Supply
title_full Emerging Infectious Diseases That Threaten the Blood Supply
title_fullStr Emerging Infectious Diseases That Threaten the Blood Supply
title_full_unstemmed Emerging Infectious Diseases That Threaten the Blood Supply
title_short Emerging Infectious Diseases That Threaten the Blood Supply
title_sort emerging infectious diseases that threaten the blood supply
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118992/
https://www.ncbi.nlm.nih.gov/pubmed/17198845
http://dx.doi.org/10.1053/j.seminhematol.2006.09.016
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