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Complement Activation During Low‐Density Lipoprotein Apheresis

机译:低密度脂蛋白单采术中的补体活化

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Abstract:Complement system activation was investigated in two girls with familial homozygous hypercholes‐terolemia undergoing two monthly sessions on LA15 or LA40 (Kaneka liposorber). We determined blood levels of C3c and C3a, leukocyte counts, and plasma levels of C3c and C3a in the extracorporeal circulation device at the start of the sessions and 15 and either 60 or 120 min into them. Sequential eluates were collected from LA40 at the end of the sessions (0.5MNaCl, 1Mhydroxylamine). Anaphylatoxin C3a increased throughout, especially with LA40. As previously reported, C3a was trapped in the dextran column but was noticeably present in efferent plasma. Besides many proteins, nonnative complement fragments bearing C3a and C3d antigens were detected in almost all the eluates, suggesting possible in situ complement activation. Practically, complement activation induced by the first filter is a risk; long‐term side effects may arise from this extracorporeal circulation dev
机译:摘要:研究了两名患有家族性纯合子高胆汁-terolemia的女孩的补体系统激活,她们每月接受两次LA15或LA40(Kaneka liposorber)治疗。我们在疗程开始时和 15 分钟和 60 分钟或 120 分钟时测定了体外循环装置中 C3c 和 C3a 的血液水平、白细胞计数以及血浆 C3c 和 C3a 水平。在疗程结束时从LA40收集顺序洗脱液(0.5MNaCl,1M羟胺)。Anphylatoxin C3a 在整个过程中增加,尤其是 LA40。正如先前报道的那样,C3a被困在葡聚糖柱中,但明显存在于传出血浆中。除了许多蛋白质外,几乎所有洗脱物中都检测到携带 C3a 和 C3d 抗原的非天然补体片段,这表明可能存在原位补体激活。实际上,由第一个过滤器诱导的补体活化是一种风险;这种体外循环开发可能会产生长期副作用

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