Mitochondrial DNA multiplex real‐time polymerase chain reaction inhibition assay for quality control of pathogen inactivation by ultraviolet C light in platelet concentrates. Issue 3 (28th December 2017)

• Record Type: Journal Article
• Authors: Kim, Sinyoung; Handke, Wiebke; Gravemann, Ute; Döscher, Andrea; Brixner, Veronika; Müller, Thomas H.; Seltsam, Axel
• Is Part Of: Transfusion. Volume 58:Issue 3(2018)
• Page Start: 758
• Page End: 765
• Publication Date: 2017-12-28
• Subjects: Hematology -- Periodicals; Blood -- Transfusion -- Periodicals; Blood Group Antigens -- Periodicals; Blood Preservation -- Periodicals; Blood Transfusion -- Periodicals; 615
• DOI: 10.1111/trf.14464
• Languages: English
• ISSNs: 0041-1132

Abstract

Abstract : BACKGROUND: Several ultraviolet (UV) light‐based pathogen inactivation (PI) technologies for platelet (PLT) products have been developed or are under development. Upon implementation of PI technologies, quality control measures are required to ensure consistent efficiency of the treatment process. Previous reports showed that amotosalen/UVA and riboflavin/UV‐based PI technologies induce modifications of the PLT‐derived mitochondrial DNA (mtDNA) that can be detected by polymerase chain reaction (PCR) inhibition assays. In this study, we sought to establish a PCR inhibition assay to document the impact of ultraviolet C (UVC) treatment with the THERAFLEX UV‐Platelets system on the mitochondrial genome in PLT concentrates (PCs). STUDY DESIGN AND METHODS: A multiplex real‐time PCR inhibition assay with simultaneous short‐amplicon (143 bp) and long‐amplicon (794 bp) amplification was developed to detect mtDNA modifications in PLTs after UVC treatment. Assay performance was tested in UVC‐treated and untreated, plasma‐reduced pooled PCs, and apheresis PCs and challenged using PCs manufactured for a clinical trial under routine‐like conditions. RESULTS: UVC illumination of PLTs resulted in dose‐dependent inhibition of mtDNA amplification for the larger amplicon. Amplification of the shorter amplicon was not affected by UVC treatment. Evaluation of 283 blinded apheresis and pooled PLT samples from routine‐like PC production resulted in prediction of UVC treatment status with 100% accuracy. CONCLUSION: The proposed dual‐amplicon size real‐time mtDNA PCR assay effectively detects nucleic acid damage induced by UVC illumination of PLTs and could be useful as an informative indicator of PI quality of the THERAFLEX UV‐Platelets system.