医学
促红细胞生成素
终末期肾病
移植
纯红细胞再生障碍
重组DNA
肾脏疾病
再生障碍
泌尿科
内科学
血液透析
贫血
生物化学
基因
化学
作者
Kearkiat Praditpornsilpa,S. Buranasot,N. Bhokaisuwan,Yingyos Avihingsanon,T. Pisitkul,Talerngsak Kansanabuch,Somchai Eiam‐Ong,Sauwaluck Chusil,T. Intarakumtornchai,Kriang Tungsanga
摘要
Since 1990, recombinant human erythropoietin(r-HuEPO) has been used for the treatment ofanaemia of chronic renal failure (CRF). Correction ofanaemia may improve cardiovascular as well as non-cardiovascular morbidity and mortality. Despite thesepotentially beneficial effects of r-HuEPO, some CRFpatients who have previously or are currently usingr-HuEPO have been reported to display suspected orconfirmed pure red cell aplasia (PRCA) [1,2]. Thesepatients developed an unexplained sudden decreasein their haemoglobin (Hgb) level. Anti-r-HuEPOantibody (Ab), which has been demonstrated in severalstudies [3–5], seems to be the proximate cause of thePRCA.Currently,thereisnofirmlyestablishedmanage-ment of anti-r-HuEPO associated with PRCA in CRFpatients. Cyclophosphamide and prednisolone appearto be ineffective [6]. We report here that anti-r-HuEPOassociated PRCA in end-stage renal disease (ESRD)patients was reversible after kidney transplantation.
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