Parvovirus B19 rebound outbreak 2024 and implications for blood- and plasma-product safety.

B19V epidemiology parvovirus B19 outbreak re‐emergence risk assessment transfusion transmission

Journal

Transfusion
ISSN: 1537-2995
Titre abrégé: Transfusion
Pays: United States
ID NLM: 0417360

Informations de publication

Date de publication:
03 Oct 2024
Historique:
revised: 04 09 2024
received: 26 07 2024
accepted: 14 09 2024
medline: 3 10 2024
pubmed: 3 10 2024
entrez: 3 10 2024
Statut: aheadofprint

Résumé

Since the beginning of 2024, several European countries reported unusually high numbers of Human parvovirus B19 (B19V) infections. An increase in B19V incidence rate might have implications for blood products for direct transfusion, however, large data sets for analysis of this outbreak are missing. B19V nucleic acid testing (NAT) of plasma donations collected between June 2018 and May 2024 from mainly Central European countries (n = 9.6 million) and the United States (n = 70.7 million) was done to the individual donation level. In Central Europe, there was a marked increase in B19V incidence from November 2023 onwards, which peaked in April 2024 with a 33-fold higher than average B19V incidence versus before the COVID-19 pandemic. In the United States, a similar trend was seen, with a yet still 6-fold lower increase than in Europe at the same time. The largest increase in B19V positivity was seen in the youngest plasma donor cohort. A B19V infection gap during the COVID-19 pandemic is likely the basis for the rebound outbreak in 2023/2024, particularly in Europe. B19V NAT of millions of plasma donations provides for large scale numbers to solidify available epidemiology insight, and to support adequate risk assessments. Based on the situation it may be prudent to consider B19V NAT for blood components specifically directed towards transfusion to higher risk recipients, or alternatively, preselecting B19V seropositive individuals or advanced age donors at higher likelihood of seropositivity and thus lower risk of virus transmission.

Sections du résumé

BACKGROUND BACKGROUND
Since the beginning of 2024, several European countries reported unusually high numbers of Human parvovirus B19 (B19V) infections. An increase in B19V incidence rate might have implications for blood products for direct transfusion, however, large data sets for analysis of this outbreak are missing.
STUDY DESIGN AND METHODS METHODS
B19V nucleic acid testing (NAT) of plasma donations collected between June 2018 and May 2024 from mainly Central European countries (n = 9.6 million) and the United States (n = 70.7 million) was done to the individual donation level.
RESULTS RESULTS
In Central Europe, there was a marked increase in B19V incidence from November 2023 onwards, which peaked in April 2024 with a 33-fold higher than average B19V incidence versus before the COVID-19 pandemic. In the United States, a similar trend was seen, with a yet still 6-fold lower increase than in Europe at the same time. The largest increase in B19V positivity was seen in the youngest plasma donor cohort.
DISCUSSION CONCLUSIONS
A B19V infection gap during the COVID-19 pandemic is likely the basis for the rebound outbreak in 2023/2024, particularly in Europe. B19V NAT of millions of plasma donations provides for large scale numbers to solidify available epidemiology insight, and to support adequate risk assessments. Based on the situation it may be prudent to consider B19V NAT for blood components specifically directed towards transfusion to higher risk recipients, or alternatively, preselecting B19V seropositive individuals or advanced age donors at higher likelihood of seropositivity and thus lower risk of virus transmission.

Identifiants

pubmed: 39360875
doi: 10.1111/trf.18032
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 The Author(s). Transfusion published by Wiley Periodicals LLC on behalf of AABB.

Références

European Centre for Disease Prevention and Control. Risks posed by reported increased circulation of human parvovirus B19 in the EU/EEA. ECDC: Stockholm (accessed September 2, 2024). 2024. https://www.ecdc.europa.eu/en/publications‐data/risks‐posed‐reported‐increased‐circulation‐human‐parvovirus‐b19‐eueea
Plasma Protein Therapeutics Association (PPTA). QSEAL NAT Testing Standard, v2.0 (Accessed September 02, 2024). https://cdn.prod.website‐files.com/638f893112c6eac0e46ac576/64517906a60bdb04ed8c3b74_NATTestingV2‐3.pdf
World Health Organization. Coronavirus disease (COVID‐19) pandemic (Accessed September 02, 2024). https://www.who.int/europe/emergencies/situations/covid-19
Wong S, Brown KE. Development of an improved method of detection of infectious parvovirus B19. J Clin Virol. 2006;3:407–413. https://doi.org/10.1016/j.jcv.2005.12.008
Guillet M, Bas A, Lacoste M, Ricard C, Visse C, Barlet V, et al. New atypical epidemiological profile of parvovirus B19 revealed by molecular screening of blood donations, France, winter 2023/24. Euro Surveill. 2024;29:2400253 https://www.eurosurveillance.org/content/10.2807/1560-7917.ES.2024.29.21.2400253
Heegaard E, Brown KE. Human parvovirus B19. Clin Microbiol Rev. 2002;15:482–505. https://doi.org/10.1128/CMR.15.3.485-505.2002
Groeneveld K, van der Noordaa J. Blood products and parvovirus B19. Neth J Med. 2003;61:154–156.
Roth NJ, Dichtelmüller HO, Fabbrizzi F, Flechsig E, Gröner A, Gustafson M, et al. Nanofiltration as a robust method contributing to viral safety of plasma‐derived therapeutics: 20 years' experience of the plasma protein manufacturers. Transfusion. 2020;60:2661–2674. https://doi.org/10.1111/trf.16022
Blümel J, Burger R, Drosten C, Groner A, Gurtler L, Heiden M, et al. Parvovirus B19 – revised: Arbeitskreis Blut, Untergruppe ‘Bewertung blutassoziierter Krankheitserreger’. Transfus Med Hemother. 2010;37:339–350. https://doi.org/10.1159/000322190
Berting A, Modrof J, Unger U, Gessner M, Klotz A, Pölsler G, et al. Inactivation of parvovirus B19 during STIM‐4 vapor heat treatment of three coagulation factor concentrates. Transfusion. 2008;48:1220–1226. https://doi.org/10.1111/j.1537-2995.2008.01662.x
Sun P, Jiang P, Liu Q, Zhang R, Wang Z, Cao H, et al. Parvovirus B19 DNA and antibodies in Chinese plasma donors, plasma pools and plasma derivatives. PeerJ. 2023;11:e15698. https://doi.org/10.7717/peerj.15698
Modrof J, Berting A, Tille B, Klotz A, Forstner C, Rieger S, et al. Neutralization of human parvovirus B19 by plasma and intravenous immunoglobulins. Transfusion. 2008;48:178–186. https://doi.org/10.1111/j.1537-2995.2007.01503.x
Aronson AT, Celiker MY, Guarini L, Agha R. Intravenous immunoglobulin treatment of congenital parvovirus B19 induced anemia – a case report. Matern Health Neonatol Perinatol. 2023;9:10. https://doi.org/10.1186/s40748‐023‐00164‐2
Kerr JR, Cunniffe VS, Kelleher P, Bernstein RM, Bruce IN. Successful intravenous immunoglobulin therapy in 3 cases of parvovirus B19‐associated chronic fatigue syndrome. Clin Infect Dis. 2003;36:e100–e106. https://doi.org/10.1086/374666
Crabol Y, Terrier B, Rozenberg F, Pestre V, Legendre C, Hermine O, et al. Intravenous immunoglobulin therapy for pure red cell aplasia related to human parvovirus B19 infection: a retrospective study of 10 patients and review of the literature. Clin Infect Dis. 2013;56:968–977. https://doi.org/10.1093/cid/cis1046

Auteurs

Maria R Farcet (MR)

Global Pathogen Safety, Takeda Manufacturing Austria AG, Vienna, Austria.

Michael Karbiener (M)

Global Pathogen Safety, Takeda Manufacturing Austria AG, Vienna, Austria.

Claudia Aberham (C)

Biolife, Takeda Manufacturing Austria AG, Vienna, Austria.

Nicholas Powers (N)

Biolife Plasma Services, Takeda, Social Circle, Georgia, USA.

Daniel Aue (D)

Biolife, Takeda Manufacturing Austria AG, Vienna, Austria.

Thomas R Kreil (TR)

Global Pathogen Safety, Takeda Manufacturing Austria AG, Vienna, Austria.

Classifications MeSH