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Acid treatment of platelets for removal of class I human leukocyte antigen (HLA) antigens

机译:血小板的酸处理以去除I类人白细胞抗原(HLA)抗原

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Acid elution of platelets class I human leukocyte antigen (HLA) antigens is considered as a strategy for production of HLA-eluted platelets for clinical use. In this study, we investigated the effects of acid treatment for the removal of class I HLA antigens on platelet activation, apoptosis and aggregation, and to evaluate the optimal elution condition and the feasibility of clinical application of the acid-elution technique. In vitro apheresis platelets from healthy volunteers were treated with various PH levels the citric acid solution (pH = 2.0, 3.0, 5.0, 7.0) at 0°C for 10 min. Expression of class I HLA antigens and P-selectin (CD62P) on platelet surface were analyzed by multicolor flow cytometry. The proportion of early apoptotic platelets was detected by Annexin V staining. The maximum platelet aggregation rate was determined by the electrical impedance aggregometry. Results showed that the expression of platelets class IHLA antigens decreased with the reduction of pH value accompanied by increase of CD62P expression and early apoptosis (Annexin V expression). When compared with phosphate buffered saline (PBS) treated platelets, platelets after elution with citric acid at pH 3.0 had significantly decreased expression of class IHLA antigens and the aggregation was not impaired, although the CD62P expression and early apoptosis were significantly increased. These results indicates that elution of platelets with citric acid at pH 3.0 can be use as an attempt to product HLA-eluted platelets for clinical use.  
机译:血小板I类人类白细胞抗原(HLA)抗原的酸洗脱被认为是生产用于临床的HLA洗脱血小板的一种策略。在这项研究中,我们研究了酸处理对I类HLA抗原的去除对血小板活化,凋亡和聚集的影响,并评估了最佳洗脱条件和酸洗脱技术在临床上的可行性。将健康志愿者的体外单采血小板在0℃下用各种PH水平的柠檬酸溶液(pH = 2.0、3.0、5.0、7.0)处理10分钟。通过多色流式细胞术分析了I类HLA抗原和P-选择蛋白(CD62P)在血小板表面的表达。通过膜联蛋白V染色检测早期凋亡血小板的比例。最大血小板凝集速率通过电阻抗聚集法测定。结果表明,血小板IHLA类抗原的表达随着pH值的降低而降低,并伴随着CD62P表达的增加和早期凋亡(Annexin V表达)的增加。与磷酸盐缓冲盐水(PBS)处理的血小板相比,用柠檬酸在pH 3.0洗脱后的血小板显着降低了IHLA类抗原的表达,并且聚集没有受到损害,尽管CD62P表达和早期凋亡明显增加。这些结果表明,在pH 3.0下用柠檬酸洗脱血小板可以用作生产HLA洗脱的血小板以供临床使用的尝试。  

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