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Nucleic acids in pathogens and contaminating leukocytes refers to the collective genomic material (DNA and RNA) of infectious agents and residual donor white blood cells found in blood components [1]. In the context of transfusion medicine, these molecules are the primary targets for pathogen inactivation technologies (PIT) designed to ensure the safety of platelets, plasma, and whole blood [2]. By targeting nucleic acids rather than specific proteins or envelopes, these technologies provide a broad-spectrum approach to neutralizing viruses, bacteria, and parasites [3]. They also prevent the proliferation of donor T-cells that cause transfusion-associated graft-versus-host disease [3]. Drugs such as amotosalen and riboflavin act as photosensitizers that intercalate into the nucleic acid structure [4]. Upon exposure to ultraviolet light, these compounds induce irreversible damage, such as covalent cross-linking or oxidative strand breaks, which prevents the replication and transcription of the genetic material [5]. This process effectively renders the pathogens and leukocytes non-infectious and immunologically inert while preserving the therapeutic function of the blood component [6].
Intercalation and photoactivation-induced covalent cross-linking or oxidative damage of DNA and RNA, preventing replication and transcription.
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