de Wit, Yasmin E S; Vlaar, Richard; Gouwerok, Eric; Hamzeh-Cognasse, Hind; van Mierlo, Gerard; Bulder, Ingrid; Lagerberg, Johan W M; de Korte, Dirk; Cognasse, Fabrice; Ten Brinke, Anja; Zeerleder, Sacha S (2023). Platelet concentrates in platelet additive solutions generate less complement activation products during storage than platelets stored in plasma. Blood transfusion, 21(2), pp. 157-167. SIMTI Servizi Srl 10.2450/2022.0323-21
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BACKGROUND
Platelet transfusions can be associated with adverse reactions, such as febrile non-haemolytic transfusion reaction (FNHTR). It has been suggested that damage-associated molecular patterns (DAMP) and complement play a role in FNHTR. This study investigated the nature of DAMPs and complement activation products contained in platelet concentrates during storage, with a specific focus on different platelet storage solutions.
MATERIALS AND METHODS
Buffy coats (BC) from healthy donors were pooled (15 BC per pool) and divided into three groups of the same volume. After addition of different storage solutions (plasma, platelet additive solutions [PAS]-C or PAS-E; n=6 for each group), BC pools were processed to platelet concentrates (PC). Leukoreduced PCs were stored on a shaking bed at 20-24°C and sampled on days 1, 2, 6 and 8 after collection for selected quality parameters: platelet activation, DAMPs (High Mobility Group Box 1 [HMGB1], nucleosomes), and complement activation products.
RESULTS
During storage, equal levels of free nucleosomes and increasing concentrations of HMGB1 were present in all groups. Complement activation was observed in all PC. However, by day 8, the use of PAS had reduced C3b/c levels by approximately 90% and C4b/c levels by approximately 65%.
DISCUSSION
Nucleosomes and HMGB1 were present in PCs prepared in plasma and PAS. Complement was activated during storage of platelets in plasma and in PAS. The use of PAS is associated with a lower amount of complement activation products due to the dilution of plasma by PAS. Therefore, PC in PAS have less complement activation products than platelets stored in plasma. These proinflammatory mediators in PC might induce FNHTR.
Item Type: |
Journal Article (Original Article) |
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Division/Institute: |
04 Faculty of Medicine > Department of Haematology, Oncology, Infectious Diseases, Laboratory Medicine and Hospital Pharmacy (DOLS) > Clinic of Haematology and Central Haematological Laboratory 04 Faculty of Medicine > Pre-clinic Human Medicine > BioMedical Research (DBMR) > Unit Childrens Hospital > Forschungsgruppe Hämatologie (Erwachsene) |
UniBE Contributor: |
Zeerleder, Sacha Sergio |
Subjects: |
600 Technology > 610 Medicine & health |
ISSN: |
1723-2007 |
Publisher: |
SIMTI Servizi Srl |
Language: |
English |
Submitter: |
Pubmed Import |
Date Deposited: |
21 Mar 2022 09:35 |
Last Modified: |
18 Mar 2023 00:11 |
Publisher DOI: |
10.2450/2022.0323-21 |
PubMed ID: |
35302481 |
BORIS DOI: |
10.48350/167645 |
URI: |
https://boris.unibe.ch/id/eprint/167645 |