Pathogen inactivation of red cell concentrates and whole blood: <scp>II</scp> . In vivo human recovery studies, clinical trials and future directions
Three technologies are currently under active development for pathogen inactivation of red cell concentrates or whole blood (WB): the Intercept technology using S-303 as an inactivating chemical; the Theraflex technology using UV-C illumination; and the Mirasol technology using riboflavin and UV light. For the UV-C technology, no in vivo data are available. For the other two technologies, recovery, survival and life span of the treated red blood cells (RBCs) are shortened but are within objective requirements, including a 24-h recovery >75%. S-303-treated RBCs were transfused in various patient groups and, so far, showed no relevant differences in the clinical endpoints. In early studies, S-303-reactive antibodies were observed, which prompted changes in the inactivation process, and no further antibody formation was seen. The one published study with the riboflavin/UV procedure showed good effectiveness of treated WB, with haemoglobin increment similar to that of untreated WB. When considering potential implementation of pathogen inactivation strategies, a balance should be struck between microbiological safety, component quality and cost. None of the current technologies is in a stage for large-scale blood bank application, either because of limited availability of evidence of satisfactory in vitro quality data or because of the ongoing requirement of clinical trials in a broad spectrum of patients.
Authors
- Pieter F. van der Meer (ORCID: https://orcid.org/0000-0002-2093-3604)
- Thomas R. Klei (ORCID: https://orcid.org/0000-0002-2864-4073)
- José A. Cancelas (ORCID: https://orcid.org/0000-0002-1291-7233)
Institutions
- Cincinnati Children's Hospital Medical Center (US)
- Harvard University (US)
- Sanquin (NL)
- Dana-Farber Cancer Institute (US)
- Emergent BioSolutions (Canada) (CA)
- Haga Hospital (NL)
- University of Cincinnati (US)
Publication Details
- Journal
- Vox Sanguinis
- Published
- 2025-10-29
- DOI
- https://doi.org/10.1111/vox.70132
- Primary Topic
- Blood transfusion and management
- Type
- article
- Field-Weighted Citation Impact
- 0.00