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鉴定血小板制剂、储存和输血反应中的新型生物活性分子,以改善输血管理。

Identification of new bioactive molecules in platelet preparation, storage, and transfusion reactions for improved transfusion management.

机构信息

Etablissement Français du Sang Auvergne-Rhône-Alpes, Saint-Étienne, France.

INSERM, Université Jean Monnet, Mines Saint-Étienne, U 1059 SAINBIOSE, F- 42023, Saint-Etienne, France.

出版信息

Sci Rep. 2024 Nov 26;14(1):29381. doi: 10.1038/s41598-024-80632-7.

Abstract

Platelet concentrates (PCs) intended for transfusion contain bioactive molecules that can be considered Biological Response Modifiers (BRMs), mainly originating from plasma regardless of the preparation process. During storage, NGAL and GDF-15 levels increase in single donor apheresis platelet concentrates (SDA-PC), whereas in buffy coat platelet concentrates (BC-PC), the levels of MIP1α, MCP-3, and HSAA increase, and GDF-15 levels decrease. These molecules, primarily released by leukocytes, may contribute to adverse reactions (ARs) following a PC transfusion. Notably, in SDA-PC or BC-PC transfusions that result in ARs, the levels of NGAL, HSAA, and GDF-15 are significantly elevated, while the levels of MDC and CX3CL1 are significantly reduced compared to transfusions without ARs. These biomarkers could potentially serve as predictors for PCs-induced ARs.

摘要

血小板浓缩物(PCs)用于输血,其中包含可被视为生物反应调节剂(BRMs)的生物活性分子,这些分子主要来源于血浆,无论制备过程如何。在储存过程中,NGAL 和 GDF-15 的水平在单采血小板浓缩物(SDA-PC)中增加,而在富含血小板的白细胞浓缩物(BC-PC)中,MIP1α、MCP-3 和 HSAA 的水平增加,GDF-15 的水平降低。这些分子主要由白细胞释放,可能导致 PC 输血后的不良反应(ARs)。值得注意的是,在导致 ARs 的 SDA-PC 或 BC-PC 输注中,NGAL、HSAA 和 GDF-15 的水平显著升高,而 MDC 和 CX3CL1 的水平与无 ARs 的输注相比显著降低。这些生物标志物可能可作为 PCs 诱导的 ARs 的预测因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5348/11599570/cb0c2115b036/41598_2024_80632_Fig1_HTML.jpg

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