Persistent aggregates in apheresis platelet concentrates

被引:10
|
作者
Feys, H. B. [1 ]
Coene, J. [2 ]
Devloo, R. [1 ]
Van Aelst, B. [1 ]
Pottel, H. [3 ]
Vandekerckhove, P. [2 ,4 ,5 ]
Compernolle, V. [1 ,2 ,5 ]
机构
[1] Belgian Red Cross Flanders, Transfus Res Ctr, B-9000 Ghent, Belgium
[2] Belgian Red Cross Flanders, Blood Serv, Mechelen, Belgium
[3] Catholic Univ Leuven KULAK, Dept Publ Hlth & Primary Care, Kortrijk, Belgium
[4] Katholieke Univ Leuven, Dept Publ Hlth & Primary Care, Leuven, Belgium
[5] Univ Ghent, Fac Med & Hlth Sci, B-9000 Ghent, Belgium
关键词
apheresis; blood collection; platelet concentrates; VON-WILLEBRAND-FACTOR; HEALTHY-INDIVIDUALS; SHEAR-STRESS; PLASMA; PROTEIN; RISK; ACTIVATION; AGITATION; QUALITY; SYSTEMS;
D O I
10.1111/vox.12243
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundAggregates often appear during apheresis. Sometimes, these persist throughout storage, causing product wastage. This study assessed product quality of apheresis concentrates containing persistent aggregates (PA) and aimed to identify the factors that contribute to their formation. MethodsDonation (n=180) and platelet indices (n10) from apheresis concentrates with PA were compared with aggregate-free products. ResultsThe proportion of donors with at least one previous PA donation was twofold higher in the PA group (P<00001) indicating a donor dependence. Significantly higher donor whole blood platelet counts (28650 vs. 266 +/- 49x10(3)/l, P<00001) and higher apheresis yields (60 +/- 16 vs. 54 +/- 15x10(11), P<00001) were noted in the PA group. Haematocrit was also slightly higher, but age, gender and body mass were similar. The pH of PA products on day six postdonation was significantly lower (P<0001), in line with higher lactic acid concentrations. Flow cytometry showed no differences in GPIb levels or phosphatidylserine exposure. However, there was slightly more integrin activation as well as increased degranulation measured by P-selectin expression. Cytokine concentrations were also significantly higher in PA concentrates. Aggregation was normal in response to SFLLRN peptide and collagen stimulation, but agglutination at low-dose ristocetin was significantly higher (P=0.01) in PA products. Finally, PA were disintegrated by plasmin-mediated thrombolysis but not by integrin (IIb3) inhibition. ConclusionProducts with PA have acceptable quality parameters, but additional functional studies are warranted. Furthermore, PA are more likely to recur in certain donors who have higher platelet counts.
引用
收藏
页码:368 / 377
页数:10
相关论文
共 50 条
  • [1] Persistent aggregates in apheresis platelet concentrates are commonly collected from donors with a history of aggregate donation
    Feys, H. B.
    Pottel, H.
    Coene, J.
    Vandewalle, G.
    Vandekerckhove, P.
    Compernolle, V.
    VOX SANGUINIS, 2016, 111 (04) : 431 - 433
  • [2] The contribution of von Willebrand factor-GPIb interactions to persistent aggregate formation in apheresis platelet concentrates
    Feys, H. B.
    Van Aelst, B.
    Devloo, R.
    Vandekerckhove, P.
    Compernolle, V.
    VOX SANGUINIS, 2016, 110 (04) : 344 - 351
  • [3] Markers of platelet activation and apoptosis in platelet concentrates collected by apheresis
    Prochazkova, Renata
    Andrys, Ctirad
    Hubackova, Lenka
    Krejsek, Jan
    TRANSFUSION AND APHERESIS SCIENCE, 2007, 37 (02) : 115 - 123
  • [4] Aggregates in platelet concentrates
    van der Meer, P. F.
    Dumont, L. J.
    Lozano, M.
    Bondar, N.
    Wong, J.
    Ismay, S.
    Pink, J.
    Nussbaumer, W.
    Coene, J.
    Feys, H. B.
    Compernolle, V.
    Devine, D. V.
    Howe, D.
    Lin, C. K.
    Sun, J.
    Ringwald, J.
    Strasser, E. F.
    Eckstein, R.
    Seltsam, A.
    Perseghin, P.
    Proserpio, P.
    Wakamoto, S.
    Akino, M.
    Takamoto, S.
    Tadokoro, K.
    Teo, D.
    Shu, P. H.
    Chua, S. S.
    Jimenez-Marco, T.
    Cid, J.
    Castro, E.
    Munoz, I.
    Gulliksson, H.
    Sandgren, P.
    Thomas, S.
    Petrik, J.
    McColl, K.
    Kamel, H.
    Dugger, J.
    Sweeney, J. D.
    Gorlin, J. B.
    Sutor, L. J.
    Heath, D.
    Sayers, M. H.
    VOX SANGUINIS, 2015, 108 (01) : 96 - 125
  • [5] Evaluation of the in vitro Function of Platelet Concentrates from Pooled Buffy Coats or Apheresis
    Fiedler, Sarah Anna
    Boller, Klaus
    Junker, Ann-Christine
    Kamp, Christel
    Hilger, Anneliese
    Schwarz, Wolfgang
    Seitz, Rainer
    Salge-Bartels, Ursula
    TRANSFUSION MEDICINE AND HEMOTHERAPY, 2020, 47 (04) : 314 - 324
  • [6] Haemostatic profile of riboflavin-treated apheresis platelet concentrates
    Petrou, Eleni
    Nikolopoulos, Georgios K.
    Kriebardis, Anastasios G.
    Pantavou, Katerina
    Loukopoulou, Electra
    Tsantes, Andreas G.
    Georgatzakou, Hara T.
    Maratou, Eirini
    Rapti, Evdoxia
    Mellou, Sofia
    Kokoris, Styliani
    Gialeraki, Argyri
    Tsantes, Argirios E.
    BLOOD TRANSFUSION, 2022, 20 (03) : 223 - 234
  • [7] Use of random versus apheresis platelet concentrates
    Andreu, G.
    Vasse, J.
    Sandid, I.
    Tardivel, R.
    Semana, G.
    TRANSFUSION CLINIQUE ET BIOLOGIQUE, 2007, 14 (06) : 514 - 521
  • [8] The effects of pathogen reduction technology on apheresis platelet concentrates stored in Pas
    Tsalas, Stavros
    Tsantes, Andreas G.
    Petrou, Eleni
    Mellou, Sofia
    Sokou, Rozeta
    Loukopoulou, Electra
    Kriebardis, Anastasios G. .
    Fortis, Sotirios P.
    Papadopoulos, Dimitrios V.
    Vaiopoulos, Aristeidis G.
    Kokoris, Styliani
    Tsantes, Argirios E.
    BLOOD TRANSFUSION, 2024, 22 (05)
  • [9] The effect of plasma removal from apheresis platelet concentrates on platelet function
    Jilma-Stohlawetz, P.
    Eichelberger, B.
    List, J.
    Jilma, B.
    Panzer, S.
    Leitner, G.
    VOX SANGUINIS, 2012, 102 (03) : 258 - 260
  • [10] Apheresis platelet concentrates contain platelet-derived and endothelial cell-derived microparticles
    Rank, A.
    Nieuwland, R.
    Liebhardt, S.
    Iberer, M.
    Gruetzner, S.
    Toth, B.
    Pihusch, R.
    VOX SANGUINIS, 2011, 100 (02) : 179 - 186