免疫血液学测试与直接抗球蛋白(Coombs)测试犬血液样本的比较研究。

Nadine Idalan, Johanna O Zeitz, Corinna N Weber, Elisabeth Müller, Urs Giger
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引用次数: 1

摘要

背景:2019年ACVIM关于犬免疫介导的溶血性贫血(IMHA)诊断的共识声明提出了测试建议。由于缺乏有关免疫血液学测试性能的数据,我们进行了比较分析。材料和方法:将126只疑似患有IMHA的狗的抗凝血液样本提交给兽医诊断实验室进行常规直接抗球蛋白试验(DAT),并对28只健康对照犬的抗凝血液样品在三次盐水洗涤前后的球细胞增多症和自凝进行评估。样品还接受了不同的DAT:临床使用的凝胶微型管和免疫层析条试剂盒;实验室中使用的中性凝胶柱卡、微量滴定板(在4°、22°和37°C下)、毛细管和流式细胞仪。结果:健康狗的样本在所有免疫诊断测试中均为阴性。在提交的126份DAT 67样本中,在22°C下,使用含有山羊抗狗抗球蛋白DAT的微量滴定板进行的DAT检测呈阳性。值得注意的是,无论使用抗球蛋白和温度如何,DAT结果在所有评估方法中都是可比较和一致的。DAT+ 与DAT-犬相比,狗的贫血更严重,更容易发生红系再生。在血液与盐水1:1和1:4稀释后的48个样品中观察到试管或载玻片中的宏观凝集,但在洗涤后仅在4个样品中持续存在。在DAT中+ 样本中,57%有凝集反应,87%有球细胞增多症,45%两者都有。球细胞增多症与来自6种DAT技术的DAT结果之间存在良好的相关性,但与自身凝集的相关性仅为中等。对42只狗进行了临床随访。来自12 DAT的样本+ 治疗期间收集的狗,10只仍为DAT+ 当在初始评估后1-24周进行测试时。结论:根据这项比较前瞻性调查,所有临床和实验室DAT技术在由受过培训的人员进行时都产生了类似的结果,因此可以推荐用于抗体包被的红细胞的检测和免疫血液学诊断。此外,使用这些测试来监测IMHA犬对治疗的反应可能是有价值的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comparative study of immunohematological tests with canine blood samples submitted for a direct antiglobulin (Coombs') test.

Comparative study of immunohematological tests with canine blood samples submitted for a direct antiglobulin (Coombs') test.

Comparative study of immunohematological tests with canine blood samples submitted for a direct antiglobulin (Coombs') test.

Comparative study of immunohematological tests with canine blood samples submitted for a direct antiglobulin (Coombs') test.

Background: A 2019 ACVIM consensus statement on diagnostics for immune-mediated hemolytic anemia (IMHA) in dogs made testing recommendations. As data on the performance of immunohematological tests was lacking, we undertook a comparative analysis.

Material and methods: Anticoagulated blood samples from 126 dogs suspected of having IMHA submitted to a diagnostic veterinary laboratory for a routine direct antiglobulin test (DAT) and from 28 healthy control dogs were evaluated for spherocytosis and autoagglutination before and after three saline washes. Samples were also subjected to different DATs: a gel minitube and an immunochromatographic strip kit used in clinics; neutral gel column cards, microtiter plates (at 4°, 22°, and 37°C), capillary tubes, and flow cytometry used in laboratories.

Results: Samples from healthy dogs yielded negative results with all immunodiagnostic tests. Among the 126 samples submitted for DAT 67 were positive by a DAT utilizing microtiter plates with goat anti-dog antiglobulin DAT at 22°C. Notably, DAT results were comparable and consistent across all evaluated methods regardless of antiglobulin and temperature used. DAT+ dogs were more severely anemic and more likely to have erythroid regeneration compared to DAT- dogs. Macroscopic agglutination in tubes or on slides was observed in 48 samples after 1:1 and 1:4 blood to saline dilution, but only persisted in four samples after washing. Among the DAT+ samples, 57% had agglutination, 87% had spherocytosis, and 45% had both. There was good correlation between spherocytosis and DAT results from the six DAT techniques, but the correlation with autoagglutination was only fair. Clinical follow-up was available for 42 dogs. Of the sample from 12 DAT+ dogs collected during treatment, 10 remained DAT+ when tested 1-24 weeks after initial assessment.

Conclusions: Based upon this comparative prospective survey, all in-clinic and laboratory DAT techniques produced similar results when performed by trained personnel and can therefore be recommended for detection of antibody-coated erythrocytes and immunohematological diagnosis. In addition, use of these tests for monitoring response of IMHA dogs to treatment might be valuable.

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