首页> 外文期刊>Nephron >Prevalence of anti-erythropoietin antibodies in hemodialysis patients without clinical signs of pure red cell aplasia. Comparison between hypo- and normoresponsive patients treated with epoetins for renal anemia.
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Prevalence of anti-erythropoietin antibodies in hemodialysis patients without clinical signs of pure red cell aplasia. Comparison between hypo- and normoresponsive patients treated with epoetins for renal anemia.

机译:在没有纯红细胞发育不良的临床征象的血液透析患者中​​,抗促红细胞生成素抗体的患病率。用依泊汀治疗肾性贫血的低反应性和正常反应性患者的比较。

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BACKGROUND/AIMS: The prevalence of anti-erythropoietin antibodies in renal patients without clinical evidence of pure red cell aplasia (PRCA) who respond poorly to epoetin is unknown. This study tested for anti-erythropoietin antibodies in hemodialysis patients who were either hypo- or normoresponsive to epoetin treatment. METHODS: Epoetin hyporesponsiveness (hemoglobin < or =10.5 g/dl and epoetin > or =9,000 IU/week) and normoresponsiveness (hemoglobin >10.5 g/dl and epoetin <7,000 IU/week) were arbitrarily defined. Prevalence of anti-erythropoietin antibodies in hemodialysis patients without symptoms of PRCA was determined by screening sera of 536 patients from 35 German KfH dialysis units, using enzyme-linked immunosorbent assay (ELISA). Positive results were verified by radioimmunoprecipitation assay (RIP) and neutralizing activity was determined by bioassay. RESULTS: Anti-erythropoietin antibodies were detected in 3 hyporesponsive and 3 normoresponsive patients using ELISA. One patient per group was verified as borderline by RIP testing; the other 4 were negative. The bioassay was negative for 1 patient; the other died unrelated to PRCA before testing. Follow-up with RIP testing after 15 months under continuous epoetin treatment was negative (4 patients, 2 deceased). CONCLUSION: This survey did not identify anti-erythropoietin antibodies in hemodialysis patient's hyporesponsive to epoetin and does not support presumptive antibody screening as a routine work-up in these patients.
机译:背景/目的:没有临床证据表明对促红细胞生成素反应较差的无纯红细胞发育不良(PRCA)的肾病患者中抗促红细胞生成素抗体的患病率尚不清楚。这项研究测试了对依泊汀治疗反应不良或正常的血液透析患者的抗促红细胞生成素抗体。方法:任意定义依泊汀低反应性(血红蛋白<或= 10.5 g / dl和epoetin>或= 9,000 IU /周)和正常反应性(血红蛋白> 10.5 g / dl和epoetin <7,000 IU /周)。通过使用酶联免疫吸附试验(ELISA)筛选35个德国KfH透析部门的536名患者的血清,确定无PRCA症状的血液透析患者中​​抗促红细胞生成素抗体的患病率。放射免疫沉淀试验(RIP)验证了阳性结果,生物测定确定了中和活性。结果:采用ELISA法检测了3例低反应性和3例正常反应性患者的抗促红细胞生成素抗体。每组一名患者通过RIP测试确认为临界点;其他4个都是负面的。 1名患者的生物测定阴性。另一名在测试前与PRCA无关。连续进行依泊汀治疗15个月后进行RIP检测的随访结果为阴性(4例患者,2例死亡)。结论:该调查未发现血液透析患者对促红细胞生成素反应低下的抗促红细胞生成素抗体,也不支持对这些患者进行常规推定性抗体筛查。

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