ReviewVox sanguinis2026
Pathogen inactivation of red cell concentrates and whole blood: II. In vivo human recovery studies, clinical trials and future directions.
Review in Vox sanguinis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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0 citing papers in PubMed.
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Authors and funding
3 authors.
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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.
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