Current perspectives in transfusion-transmitted infectious diseases: emerging and re-emerging infections
- PMID: 25210533
- PMCID: PMC4142007
- DOI: 10.1111/voxs.12070
Current perspectives in transfusion-transmitted infectious diseases: emerging and re-emerging infections
Abstract
Background: In August 2009, a group from the AABB (Stramer et al., Transfusion 2009;99:1S-29S, Emerging Infectious Disease Agents and their Potential Threat to Transfusion Safety; http://www.aabb.org/resources/bct/eid/Pages/default.aspx) published a Supplement to Transfusion that reviewed emerging infectious disease (EID) agents that pose a real or theoretical threat to transfusion safety, but for which an existing effective intervention is lacking. The necessary attributes for transfusion transmission were outlined including: presence of the agent in blood during the donor's asymptomatic phase, the agent's survival/persistence in blood during processing/storage, and lastly that the agent must be recognized as responsible for a clinically apparent outcome in at least a proportion of recipients who become infected. Without these attributes, agents are not considered as a transfusion-transmission threat and were excluded. Sixty-eight such agents were identified with enough evidence/likelihood of transfusion transmission (e.g., blood phase) and potential for clinical disease to warrant further consideration. In the Supplement, Fact Sheets (FS) were published providing information on: agent classification; disease agent's importance; clinical syndromes/diseases caused; transmission modes (including vectors/reservoirs); likelihood of transfusion transmission, and if proven to be transfusion-transmitted, information on known cases; the feasibility/predicted success of interventions for donor screening (questioning) and tests available for diagnostics/ adapted for donor screening; and finally, the efficacy, if known, of inactivation methods for plasma-derived products. The Supplement included a separate section on pathogen reduction using published data. Agents were prioritized relative to their scientific/epidemiologic threat and their perceived threat to the community including concerns expressed by the regulators of blood. Agents given the highest priority due to a known transfusion-transmission threat and severe/fatal disease in recipients were the vCJD prion, dengue viruses and the obligate red-cell parasite that causes babesiosis (B. microti and related Babesia). Although the focus of the Supplement was towards the United States and Canada, many of the agents (and the process) are applicable worldwide.
Next steps: Since the publication of the Supplement, six new FSs (yellow fever viruses-including vaccine breakthrough infections, miscellaneous arboviruses, XMRV, human parvoviruses/bocaviruses other than B19, and most recently the Middle East respiratory syndrome coronavirus, MERS-CoV) were added and 14 existing FSs updated (Anaplasma, Babesia, Bartonella, Erhlichia, chronic wasting disease-CWD, human prions other than vCJD, vCJD, Coxiella burnetii-the agent of Q fever, dengue viruses, HAV, HEV, Japanese encephalitis-JE complex, tick-borne encephalitis viruses-TBEV, and human parvovirus B19). Also, tables were released outlining pathogen reduction clinical trials/results (published) and availability/commercial routine use of such technologies by country. Of necessity, the list of EID agents is not, and can never be, complete due to the nature of emergence. We recognized that a system of assessing the risk/threat of EIDs for their potential impact on blood safety and availability must include processes for monitoring, identifying, evaluating, estimating severity, assessing risk and developing interventions. Thus, a 'toolkit' containing the necessary 'tools' from EID monitoring (horizon scanning) to validation/effectiveness evaluations of interventions is being developed. The goal is, to develop a systematic approach to risk assessment and intervention development for the impact of emerging infectious upon blood safety intended to educate and provide advise about risks/interventions in a timely/accurate fashion.
Conclusions: The process and final product (toolkit) including methods to monitor EID agent emergence, identification/recognition of a transfusion-transmission threat, methods for quantitative risk assessments, and the appropriate management of such threats should be considered for implementation by all blood systems.
Keywords: blood donation testing; epidemiology; transfusion; transmissible infections.
Similar articles
-
[Single-donor (apheresis) platelets and pooled whole-blood-derived platelets--significance and assessment of both blood products].Clin Lab. 2014;60(4):S1-39. doi: 10.7754/clin.lab.2014.140210. Clin Lab. 2014. PMID: 24779310 Review. German.
-
Emerging infectious disease agents and their potential threat to transfusion safety.Transfusion. 2009 Aug;49 Suppl 2:1S-29S. doi: 10.1111/j.1537-2995.2009.02279.x. Transfusion. 2009. PMID: 19686562
-
The future of Cochrane Neonatal.Early Hum Dev. 2020 Nov;150:105191. doi: 10.1016/j.earlhumdev.2020.105191. Epub 2020 Sep 12. Early Hum Dev. 2020. PMID: 33036834
-
Transfusion-transmitted arboviruses: Update and systematic review.PLoS Negl Trop Dis. 2022 Oct 6;16(10):e0010843. doi: 10.1371/journal.pntd.0010843. eCollection 2022 Oct. PLoS Negl Trop Dis. 2022. PMID: 36201547 Free PMC article.
-
Transfusion-transmitted tick-borne infections: a cornucopia of threats.Transfus Med Rev. 2004 Oct;18(4):293-306. doi: 10.1016/j.tmrv.2004.07.001. Transfus Med Rev. 2004. PMID: 15497129 Review.
Cited by
-
Clinical Laboratory Biosafety Gaps: Lessons Learned from Past Outbreaks Reveal a Path to a Safer Future.Clin Microbiol Rev. 2021 Jun 16;34(3):e0012618. doi: 10.1128/CMR.00126-18. Epub 2021 Jun 9. Clin Microbiol Rev. 2021. PMID: 34105993 Free PMC article. Review.
-
Educational Case: Babesiosis and Transfusion-Transmitted Infections.Acad Pathol. 2020 Jul 17;7:2374289520935591. doi: 10.1177/2374289520935591. eCollection 2020 Jan-Dec. Acad Pathol. 2020. PMID: 32733991 Free PMC article.
-
Climate change projections of West Nile virus infections in Europe: implications for blood safety practices.Environ Health. 2016 Mar 8;15 Suppl 1(Suppl 1):28. doi: 10.1186/s12940-016-0105-4. Environ Health. 2016. PMID: 26961903 Free PMC article.
-
Viral metagenomics and blood safety.Transfus Clin Biol. 2016 Feb;23(1):28-38. doi: 10.1016/j.tracli.2015.12.002. Epub 2016 Jan 9. Transfus Clin Biol. 2016. PMID: 26778104 Free PMC article. Review.
-
Proceedings of the Food and Drug Administration public workshop on pathogen reduction technologies for blood safety 2018 (Commentary, p. 3026).Transfusion. 2019 Sep;59(9):3002-3025. doi: 10.1111/trf.15344. Epub 2019 May 29. Transfusion. 2019. PMID: 31144334 Free PMC article. No abstract available.
References
-
- Stramer SL, Hollinger FB, Katz LM, et al. Emerging infectious disease agents and their potential threat to transfusion safety. Transfusion. 2009;49:1S–29S. http://www.aabb.org/resources/bct/eid/Pages/default.aspx. Last accessed 9 Dec 2013. - PubMed
-
- Semenza JC, Domanović D. Commentary; blood supply under threat. Nature Clim Change. 2013;3:1–6.
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Research Materials