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单采血小板和富血小板血浆中残余红细胞上的恒河猴D抗原决定簇

Rhesus D Antigenic Determinants on Residual Red Blood Cells in Apheresis and Buffy Coat Platelet Concentrates.

作者信息

Thibault Louis, de Grandmont Marie Joëlle, Cayer Marie-Pierre, Dussault Nathalie, Jacques Annie, Ducas Eric, Beauséjour Annie, Lebrun André

机构信息

Héma-Québec, Medical Affairs and Innovation, Québec, Québec, Canada.

Héma-Québec, Medical Affairs and Innovation, Montréal, Québec, Canada.

出版信息

Transfus Med Hemother. 2020 Apr;47(2):129-134. doi: 10.1159/000501106. Epub 2019 Jun 27.

Abstract

BACKGROUND

The level of residual red blood cells (RBCs) in platelet concentrates (PCs) is of interest because of clinical concerns related to alloimmunization to RBC antigens in transfused patients. This work aims at characterizing and quantifying the levels of intact and fragmented RBCs in apheresis (AP-PCs) and buffy coat PCs (BC-PCs) to assess their potential risk for RhD antigen alloimmunization.

METHODS

After staining with anti-CD41 (platelets) and anti-CD235a (RBCs) antibodies, the size and density of RhD antigen on intact and fragmented RBCs were analyzed by flow cytometry.

RESULTS

Residual RBC counts were 29 ± 22 × 10/unit in AP-PCs and 121 ± 54 × 10/unit in BC-PCs, which correspond to about 3 and 11 µL of RBCs by product, respectively. RhD expression was about 4 times higher on RBC particles in AP-PCs, and these particles contribute to 66 and 75% of the total antigenic load in BC-PCs and AP-PCs, respectively.

CONCLUSIONS

Processing methods influence the quantity and nature of contaminating residual RBCs and RBC-derived particles in PCs. The estimation of residual RBCs in these blood products is generally based on measurements of intact RBCs, which might underestimate the risk for alloim-munization in transfused patients. The question of whether these RBC-derived particles can produce an immune response and, thus, should then be taken into consideration for Rh immune prophylactic treatments, remains to be clarified.

摘要

背景

由于临床关注输血患者对红细胞(RBC)抗原的同种免疫,血小板浓缩物(PCs)中残余红细胞(RBCs)的水平备受关注。本研究旨在对单采血小板(AP - PCs)和 Buffy 层血小板(BC - PCs)中完整和破碎红细胞的水平进行表征和定量,以评估其对 RhD 抗原同种免疫的潜在风险。

方法

用抗 CD41(血小板)和抗 CD235a(RBCs)抗体染色后,通过流式细胞术分析完整和破碎 RBCs 上 RhD 抗原的大小和密度。

结果

AP - PCs 中残余 RBC 计数为 29 ± 22 × 10⁶/单位,BC - PCs 中为 121 ± 54 × 10⁶/单位,按产品计算分别相当于约 3 和 11 μL 的 RBCs。AP - PCs 中 RBC 颗粒上的 RhD 表达约高 4 倍,这些颗粒分别占 BC - PCs 和 AP - PCs 总抗原负荷的 66%和 75%。

结论

处理方法会影响 PC 中污染的残余 RBCs 和 RBC 衍生颗粒的数量和性质。这些血液制品中残余 RBCs 的估计通常基于完整 RBCs 的测量,这可能低估了输血患者同种免疫的风险。这些 RBC 衍生颗粒是否能产生免疫反应,进而在 Rh 免疫预防性治疗中应予以考虑,这一问题仍有待阐明。

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Understanding red blood cell alloimmunization triggers.了解红细胞同种免疫的触发因素。
Hematology Am Soc Hematol Educ Program. 2016 Dec 2;2016(1):446-451. doi: 10.1182/asheducation-2016.1.446.
4
I am the 9%: Making the case for whole-blood platelets.我是那9%:支持全血血小板的理由
Transfus Med. 2016 Jun;26(3):177-85. doi: 10.1111/tme.12312. Epub 2016 May 12.

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