小儿心脏移植术中异血凝素与人白细胞抗原去除技术的体外比较

Emily A Hayes, Ashley B Walczak, Erin Goodhue Meyer, Kathleen K Nichol, Matthew A Deitemyer, V. Duffy, Michelle Moore Padilla, Robert J Gajarski, D. Nandi
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摘要

背景:高度敏感的儿科患者等待心脏移植的等待时间更长,等待名单死亡率更高。为了提高移植成功的可能性,已经采用了各种策略,包括围手术期血浆置换,以扩大潜在的供体池。方法:本体外研究采用两种膜质血浆分离(MP、Prismaflex)和两种离心质血浆分离(CP、Spectra Optia、Terumo BCT)回路,将其合并到四个独立的体外(EC)回路中,并注入高效价、高敏化的O型供体全血。测定基线抗a和B等血凝素滴度(IT)和抗人白细胞抗原(HLA)抗体,然后每30分钟增加一次,直到2小时结束。结果:MP和CP组抗a、抗b IgM和IgG滴度均下降,MP和CP组抗a、抗b滴度平均分别下降4.625滴度(变化93.7%)和4.375滴度(变化93.8%)。分离2小时时,CP使平均荧光强度(MFI)降低2-3.5倍,MP使MFI降低1.7-2.5倍。结论:在体外血浆分离IT - hla抗体降低模型中,MP和CP均能快速有效地降低循环抗体,且CP可能具有更大程度的效率。需要在移植时将CP或MP纳入EC电路的进一步体内研究。然而,随着进一步的临床研究,有可能扩大潜在的供体并提高敏感患者的患者安全性。
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An in Vitro Comparison of Intra-Operative Isohemagglutinin and Human Leukocyte Antigen Removal Techniques in Pediatric Heart Transplant
Background: Highly sensitized pediatric patients awaiting heart transplantation experience longer wait times and higher waitlist mortality. To improve the likelihood of successful transplantation, various strategies have been utilized, including peri-operative plasmapheresis, to broaden potential donor pools. Methods: This in vitro study utilized two membrane-based plasmapheresis (MP, Prismaflex) and two centrifuge-based plasmapheresis (CP, Spectra Optia, Terumo BCT) circuits incorporated into four separate extracorporeal (EC) circuits primed with high titer, highly sensitized type O donor whole blood. Assays were performed to determine baseline anti-A and B isohemagglutinin titers (IT) and anti-human leukocyte antigen (HLA) antibodies and then at 30-minute increments until completion of the run at two hours. Results:  There was a decrease in anti-A and anti-B IgM and IgG titers with both MP and CP.  Mean anti-A and anti-B titer reduction was by 4.625 titers (93.7% change) and 4.375 titers (93.8% change) using MP and CP, respectively.  At two hours of apheresis, CP reduced mean fluorescence intensity (MFI) by 2-3.5 fold and MP reduced MFI by 1.7-2.5 fold. Conclusions: In this in vitro plasmapheresis model of IT and anti-HLA antibody reduction, both MP and CP can be used quickly and effectively to reduce circulating antibodies, and CP may have some greater degree of efficiency. Further in vivo research on incorporating CP or MP into EC circuits at the time of transplant is needed. However, with further clinical research, there is potential to broaden potential donors and improve patient safety in sensistized patients.
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