Preventing Transfusion-Transmitted Babesiosis
- PMID: 34578209
- PMCID: PMC8468711
- DOI: 10.3390/pathogens10091176
Preventing Transfusion-Transmitted Babesiosis
Abstract
Babesia are tick-borne intra-erythrocytic parasites and the causative agents of babesiosis. Babesia, which are readily transfusion transmissible, gained recognition as a major risk to the blood supply, particularly in the United States (US), where Babesia microti is endemic. Many of those infected with Babesia remain asymptomatic and parasitemia may persist for months or even years following infection, such that seemingly healthy blood donors are unaware of their infection. By contrast, transfusion recipients are at high risk of severe babesiosis, accounting for the high morbidity and mortality (~19%) observed in transfusion-transmitted babesiosis (TTB). An increase in cases of tick-borne babesiosis and TTB prompted over a decade-long investment in blood donor surveillance, research, and assay development to quantify and contend with TTB. This culminated in the adoption of regional blood donor testing in the US. We describe the evolution of the response to TTB in the US and offer some insight into the risk of TTB in other countries. Not only has this response advanced blood safety, it has accelerated the development of novel serological and molecular assays that may be applied broadly, affording insight into the global epidemiology and immunopathogenesis of human babesiosis.
Keywords: Babesia; babesiosis; blood transfusion; prevention; screening.
Conflict of interest statement
EMB reports personal fees and nonfinancial support from Terumo BCT, Grifols Diagnostics Solutions, and Abbott Laboratories outside of the submitted work; EMB is a member of the United States Food and Drug Administration (FDA) Blood Products Advisory Committee. Any views or opinions that are expressed in this manuscript are that of the author’s, based on his own scientific expertise and professional judgment; they do not necessarily represent the views of either the Blood Products Advisory Committee or the formal position of FDA, and also do not bind or otherwise obligate or commit either the Advisory Committee or the Agency to the views expressed. PJK reports research collaboration with Gold Standard Diagnostics. LT has no relevant conflicts of interest to disclose.
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