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.

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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
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article

Pathogen inactivation of red cell concentrates and whole blood: II . In vivo human recovery studies, clinical trials and future directions

Pieter F. van der Meer, Thomas R. Klei, José A. Cancelas
Vox Sanguinis
Blood transfusion and management
article

Pathogen inactivation of red cell concentrates and whole blood: II . In vivo human recovery studies, clinical trials and future directions

Pieter F. van der Meer, Thomas R. Klei, José A. Cancelas
article en

Abstract

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.

Vox SanguinisVol. 121(1)
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)
Openalex Percentile: Top 70%
Blood transfusion and management
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Pathogen inactivation of red cell concentrates and whole blood: <scp>II</scp> . In vivo human recovery studies, clinical trials and future directions — Pieter F. van der Meer, Thomas R. Klei, et al. · Vox Sanguinis (2025) | TGRS Research Map | TGRS