Little C, Rumsby M G
Scand J Haematol. 1980 Aug;25(2):134-40. doi: 10.1111/j.1600-0609.1981.tb01378.x.
Blood from 5 patients suffering from hereditary spherocytosis (HS) was stored in acid-citrate-dextrose anticoagulant at 4 degrees C for up to 6 weeks. The erythrocyte morphology and susceptibility to lysis by phospholipase C (Bacillus cereus) were examined at 2-weekly intervals and compared with erythrocytes from 6 different donations of stored normal blood. the hereditary spherocytes went through essentially the same series of morphological changes as did normal erythrocytes. Fresh hereditary spherocytes were very resistant to lysis by phospholipase C, but, like normal erythrocytes, became progressively more susceptible to lysis upon storage. In terms of erythrocyte morphological changes and development of susceptibility to lysis by the enzyme, blood from HS patients aged less rapidly than did normal blood. Splenectomy appeared to have no marked effect on the storage properties of blood from these patients as indicated by erythrocyte morphology and susceptibility to lysis by phospholipase C.
将5例遗传性球形红细胞增多症(HS)患者的血液置于含酸-柠檬酸-葡萄糖抗凝剂中,在4℃下保存长达6周。每隔2周检查红细胞形态以及对磷脂酶C(蜡样芽孢杆菌)裂解的敏感性,并与6份不同的正常献血者的储存血液中的红细胞进行比较。遗传性球形红细胞经历了与正常红细胞基本相同的一系列形态变化。新鲜的遗传性球形红细胞对磷脂酶C的裂解具有很强的抵抗力,但与正常红细胞一样,在储存过程中对裂解的敏感性逐渐增加。就红细胞形态变化和对该酶裂解敏感性的发展而言,HS患者的血液比正常血液老化得慢。红细胞形态和对磷脂酶C裂解的敏感性表明,脾切除术对这些患者血液的储存特性似乎没有明显影响。