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采用补体依赖性细胞毒性测量 ABO 抗体的一项新试验。

A New Trial to Measure ABO Antibodies Using Complement-Dependent Cytotoxicity.

机构信息

Department of Laboratory Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.

Department of Laboratory Medicine, Kangdong Sacred Heart Hospital, Seoul 05355, Korea.

出版信息

Medicina (Kaunas). 2022 Jun 20;58(6):830. doi: 10.3390/medicina58060830.

Abstract

Background and objectives: The ABO antibody (Ab) titration tests are used in monitoring in ABO-incompatible (ABOi) solid organ transplantation (SOT). However, currently developed ABO Ab tests show Ab binding reactions. This study attempted to measure ABO Ab level using complement-dependent cytotoxicity (CDC). Materials and methods: We studied 93 blood group O serum samples from patients who underwent ABOi SOT from January 2019 to May 2021. Patients’ sera were incubated with A1 or B cells and added to a human complement solution. Supernatants were collected after centrifugation, and free hemoglobin (Hb) was measured by spectrophotometry. We converted plasma Hb value to hemolysis (%), which were compared with ABO Ab titer. Results: We found a mild correlation between hemolysis and ABO Ab titers. In simple regression analysis, the correlation coefficients were within 0.3660−0.4968 (p < 0.0001) before transplantation. In multiple linear regression analysis, anti-A hemolysis (%) was higher in immunoglobulin M (IgM) (β = 12.9) than in immunoglobulin G (IgG) (β = −3.4) (R2 = 0.5216). Anti-B hemolysis was higher in IgM (β = 8.7) than in IgG (β = 0.0) (R2 = 0.5114). There was a large variation in hemolysis within the same Ab titer. Conclusions: CDC can be used in a new trial for ABO Ab measurement. Furthermore, IgM rather than IgG seems to play a significant role in vivo activity, consistent with previous knowledge. Thus, this study may help in the development of the ABO Ab titration supplement test for post-transplant treatment policy establishment and pre-transplant desensitization.

摘要

背景与目的

ABO 抗体(Ab)滴定试验用于监测 ABO 不相容(ABOi)实体器官移植(SOT)中的情况。然而,目前开发的 ABO Ab 试验仅显示 Ab 结合反应。本研究试图使用补体依赖性细胞毒性(CDC)来测量 ABO Ab 水平。

材料与方法

我们研究了 93 例来自 2019 年 1 月至 2021 年 5 月期间接受 ABOi SOT 的 O 型血患者的血清样本。将患者的血清与 A1 或 B 细胞孵育,并加入人补体溶液。离心后收集上清液,并通过分光光度法测量游离血红蛋白(Hb)。我们将血浆 Hb 值转换为溶血(%),并与 ABO Ab 滴度进行比较。

结果

我们发现溶血与 ABO Ab 滴度之间存在轻度相关性。在简单回归分析中,移植前的相关系数在 0.3660−0.4968 之间(p<0.0001)。在多元线性回归分析中,抗-A 溶血(%)在免疫球蛋白 M(IgM)(β=12.9)中高于免疫球蛋白 G(IgG)(β=−3.4)(R2=0.5216)。抗-B 溶血在 IgM(β=8.7)中高于 IgG(β=0.0)(R2=0.5114)。在相同的 Ab 滴度内,溶血存在较大的差异。

结论

CDC 可用于 ABO Ab 测量的新试验。此外,与以往的知识一致,IgM 而不是 IgG 似乎在体内活性中起重要作用。因此,本研究可能有助于开发 ABO Ab 滴定补充试验,以制定移植后治疗策略和移植前脱敏方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a74/9231086/131ed929e29b/medicina-58-00830-g001.jpg

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