Cold storage alters the immune characteristics of platelets and potentiates bacterial‐induced aggregation. Issue 8 (17th May 2022)

• Record Type: Journal Article
• Authors: Winskel‐Wood, Ben; Padula, Matthew P.; Marks, Denese C.; Johnson, Lacey
• Is Part Of: Vox sanguinis. Volume 117:Issue 8(2022)
• Page Start: 1006
• Page End: 1015
• Publication Date: 2022-05-17
• Subjects: bacteria -- cold storage -- immunology -- platelets; Blood -- Periodicals; Blood -- Transfusion -- Periodicals; Immunohematology -- Periodicals; Immunopathology -- Periodicals; 615.39
• DOI: 10.1111/vox.13293
• Languages: English
• ISSNs: 0042-9007

Abstract

Abstract: Background and Objectives: Cold‐stored platelets are currently under clinical evaluation and have been approved for limited clinical use in the United States. Most studies have focused on the haemostatic functionality of cold‐stored platelets; however, limited information is available examining changes to their immune function. Materials and Methods: Two buffy‐coat‐derived platelet components were combined and split into two treatment arms: room temperature (RT)‐stored (20–24°C) or refrigerated (cold‐stored, 2–6°C). The concentration of select soluble factors was measured in the supernatant using commercial ELISA kits. The abundance of surface receptors associated with immunological function was assessed by flow cytometry. Platelet aggregation was assessed in response to Escherichia coli and Staphylococcus aureus, in the presence and absence of RGDS (blocks active conformation of integrin α2 β3 ). Results: Cold‐stored platelet components contained a lower supernatant concentration of C3a, RANTES and PF4. The abundance of surface‐bound P‐selectin and integrin α2 β3 in the activated conformation increased during cold storage. In comparison, the abundance of CD86, CD44, ICAM‐2, CD40, TLR1, TLR2, TLR4, TLR3, TLR7 and TLR9 was lower on the surface membrane of cold‐stored platelets compared to RT‐stored components. Cold‐stored platelets exhibited an increased responsiveness to E. coli‐ and S. aureus ‐induced aggregation compared to RT‐stored platelets. Inhibition of the active conformation of integrin α2 β3 using RGDS reduced the potentiation of bacterial‐induced aggregation in cold‐stored platelets. Conclusion: Our data highlight that cold storage changes the in vitro immune characteristics of platelets, including their sensitivity to bacterial‐induced aggregation. Changes in these immune characteristics may have clinical implications post transfusion.