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新输血患者中肾衰竭与红细胞同种免疫的关系。

Association between renal failure and red blood cell alloimmunization among newly transfused patients.

机构信息

Center for Clinical Transfusion Research, Sanquin Research, Leiden, The Netherlands.

Department of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, The Netherlands.

出版信息

Transfusion. 2021 Jan;61(1):35-41. doi: 10.1111/trf.16166. Epub 2020 Dec 9.

Abstract

BACKGROUND

Renal failure and renal replacement therapy (RRT) affect the immune system and could therefore modulate red blood cell (RBC) alloimmunization after transfusion.

STUDY DESIGN AND METHODS

We performed a nationwide multicenter case-control study within a source population of newly transfused patients between 2005 and 2015. Using conditional multivariate logistic regression, we compared first-time transfusion-induced RBC alloantibody formers (N = 505) with two nonalloimmunized recipients with similar transfusion burden (N = 1010).

RESULTS

Renal failure was observed in 17% of the control and 13% of the case patients. A total of 41% of the control patients and 34% of case patients underwent acute RRT. Renal failure without RRT was associated with lower alloimmunization risks after blood transfusion (moderate renal failure: adjusted relative rate [RR], 0.82 [95% confidence interval (CI), 0.67-1.01]); severe renal failure, adjusted RR, 0.76 [95% CI, 0.55-1.05]). With severe renal failure patients mainly receiving RRT, the lowest alloimmunization risk was found in particularly these patients [adjusted RR 0.48 (95% CI 0.39-0.58)]. This was similar for patients receiving RRT for acute or chronic renal failure (adjusted RR, 0.59 [95% CI, 0.46-0.75]); and adjusted RR, 0.62 [95% CI 0.45-0.88], respectively).

CONCLUSION

These findings are indicative of a weakened humoral response in acute as well as chronic renal failure, which appeared to be most pronounced when treated with RRT. Future research should focus on how renal failure and RRT mechanistically modulate RBC alloimmunization.

摘要

背景

肾衰竭和肾脏替代治疗(RRT)会影响免疫系统,因此可能会调节输血后的红细胞(RBC)同种免疫。

研究设计和方法

我们在 2005 年至 2015 年间的新输血患者源人群中进行了一项全国性多中心病例对照研究。使用条件多变量逻辑回归,我们将首次输血诱导 RBC 同种异体抗体形成者(N=505)与具有相似输血负担的两名非同种免疫受者(N=1010)进行比较。

结果

在对照组和病例组中分别有 17%和 13%的患者出现肾衰竭。41%的对照组患者和 34%的病例组患者接受了急性 RRT。无 RRT 的肾衰竭与输血后同种免疫风险降低相关(中度肾衰竭:调整后的相对风险[RR],0.82[95%置信区间[CI],0.67-1.01];严重肾衰竭,调整后的 RR,0.76[95% CI,0.55-1.05])。由于严重肾衰竭患者主要接受 RRT,因此发现这些患者的同种免疫风险最低[调整后的 RR 0.48(95% CI 0.39-0.58)]。对于接受急性或慢性肾衰竭 RRT 的患者,情况类似(调整后的 RR,0.59[95% CI,0.46-0.75]);调整后的 RR,0.62[95% CI,0.45-0.88])。

结论

这些发现表明急性和慢性肾衰竭均会导致体液免疫反应减弱,而当接受 RRT 治疗时,这种反应似乎最为明显。未来的研究应重点关注肾衰竭和 RRT 如何在机制上调节 RBC 同种免疫。

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