Inactivation of yellow fever virus with amotosalen and ultraviolet A light pathogen-reduction technology.

Abstract

BACKGROUNDThe reemergence of yellow fever virus (YFV) in Africa and Brazil, and massive vaccine campaigns triggered to contain the outbreaks, have raised concerns over blood transfusion safety and availability with increased risk of YFV transfusion‐transmitted infections (TTIs) by native and vaccine‐acquired YFV. Blood donor deferral for 2 to 4 weeks following live attenuated YFV vaccination, and deferral for travel to endemic/epidemic areas, may result in blood donor loss and impact platelet component (PC) stocks. This study investigated the efficacy of INTERCEPT Blood System pathogen reduction (PR) with use of amotosalen and ultraviolet A (UVA) light to inactivate high levels of YFV in PCs.MATERIALSFour units of apheresis platelets prepared in 35% plasma/65% platelet additive solution (PC‐PAS) and 4 units of PC in 100% human plasma (PC‐Plasma) were spiked with high infectious titers of YFV (YFV‐17D vaccine strain). YFV‐17D infectious titers were measured by plaque assay and expressed as plaque‐forming units (PFU) before and after amotosalen/UVA treatment to determine log reduction.RESULTSThe mean YFV‐17D infectious titers in PC before inactivation were 5.5 ± 0.1 log PFU/mL in PC‐PAS and 5.3 ± 0.1 log PFU/mL in PC‐Plasma. No infectivity was detected immediately after amotosalen/UVA treatment.CONCLUSIONThe amotosalen/UVA PR system inactivated high titers of infectious YFV‐17D in PC. This PR technology could reduce the risk of YFV TTI and help secure PC supplies in areas experiencing YFV outbreaks where massive vaccination campaigns are required.