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Expanded Panel of Cytometric Markers for Canine Immune Thrombocytopenia

机译:犬免疫血小板减少症的膨胀组细胞计数标志物

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Platelet count alone is not predictive of bleeding severity or response to treatment for dogs with ITP. We evaluated dogs with severe thrombocytopenia to identify platelet abnormalities with potential diagnostic or prognostic relevance.Flow cytometric assays detected platelet membrane-bound IgG and IgM (PsAIg), fibrinogen receptor (CD61) expression, and phosphatidylserine (PS) externalization. Microspheres conjugated with defined concentrations of canine immunoglobulin were used as assay controls. To assess sample stability, replicate analyses were performed on EDTA blood samples from healthy dogs (n=7) through 72 hours of storage. Pre-treatment samples were also analyzed within 48 hours of collection from 21 dogs with severe thrombocytopenia (<50,000 platelets/ uL) in 3 categories: primary/autoimmune (PI, n=7); infectious/lymphoproliferative/drug-associated secondary immune (SI, n=7); non-immune (NI, n=7) due to consumption or bone marrow suppression.
机译:仅单独的血小板计数未预测出血的严重程度或对ITP的狗治疗的反应。我们评估了严重的血小板减少症的狗,以鉴定患有诊断或预后相关性的血小板异常。流动计量测定检测到的血小板膜结合的IgG和IgM(PSAIG),纤维蛋白原受体(CD61)表达和磷脂酰丝氨酸(PS)外化。用定义浓度的犬免疫球蛋白缀合的微球被用作测定对照。为了评估样品稳定性,在EDTA血液样本中从健康犬(n = 7)通过72小时的储存来进行复制分析。还在收集的预处理样品从21只血小板(<50,000个血小板/ UL)的21只犬中的3个分类:主要/自身免疫(PI,N = 7);感染性/淋巴抑制剂/药物相关的二级免疫(Si,N = 7);由于消耗或骨髓抑制,非免疫(Ni,N = 7)。

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