Department of Clinical Sciences, Faculty of Veterinary Medicine, Université de Montréal, Saint-Hyacinthe, QC, Canada.
Department of Clinical Sciences, Bailey Small Animal Teaching Hospital, College of Veterinary Medicine, Auburn University, Auburn, AL, USA.
J Feline Med Surg. 2022 Jun;24(6):e124-e130. doi: 10.1177/1098612X221094502. Epub 2022 May 5.
The aim of this study was to characterize anti-feline erythrocyte antigen (FEA) 1 alloantibodies following sensitization of FEA 1-negative cats, including their rate of appearance, agglutination titer over time and immunoglobulin class. A secondary aim was to obtain polyclonal anti-FEA 1 alloantibodies to increase the availability of FEA 1 blood typing. We also describe a case study documenting an acute hemolytic transfusion reaction in a transfusion-naive FEA 1-negative feline patient that received FEA 1-positive blood.
In this prospective clinical study, 35 cats with blood group type A underwent extensive blood typing for FEA 1-5. Two cats were identified as FEA 1-negative; these cats were transfused uneventfully with 50 ml of FEA 1-positive, but otherwise compatible, packed red blood cells. Post-transfusion blood samples were collected routinely as long as anti-FEA 1 alloantibodies were detected. Appearance of anti-FEA 1 alloantibodies was detected using a gel column crossmatch method.
Anti-FEA 1 alloantibodies were detected as early as 5 days post-transfusion and remained detectable for over 400 days in one cat. Agglutination titers in both cats were relatively weak (1:1 to 1:8). The main immunoglobulin class was IgM.
Transfusion of FEA 1-negative, transfusion-naive cats with FEA 1-positive blood results in production of post-transfusion anti-FEA 1 alloantibodies as early as 5 days post-transfusion. Our results confirm the potential immunogenicity of FEA 1 and support crossmatching prior to a blood transfusion, even in transfusion-naive cats. Further studies are needed to better document the clinical importance of these post-transfusion antibodies, as well as to facilitate routine blood typing for the FEA 1 antigen in cats.
本研究旨在描述 FEA1 阴性猫致敏后抗猫红细胞抗原(FEA)1 同种抗体的特征,包括其出现的速度、随时间推移的凝集效价和免疫球蛋白类别。次要目的是获得多克隆抗 FEA1 同种抗体,以增加 FEA1 血型鉴定的可用性。我们还描述了一个病例研究,记录了一例接受 FEA1 阳性血液的初次输血的 FEA1 阴性猫患者发生的急性溶血性输血反应。
在这项前瞻性临床研究中,35 只 A 型血猫进行了广泛的 FEA1-5 血型鉴定。有 2 只猫被鉴定为 FEA1 阴性;这些猫接受了 50ml FEA1 阳性但其他方面相容的浓缩红细胞输注,过程顺利。只要检测到抗 FEA1 同种抗体,就定期采集输血后血样。使用凝胶柱交叉配血法检测抗 FEA1 同种抗体的出现。
抗 FEA1 同种抗体早在输血后 5 天就被检测到,在一只猫中可检测到超过 400 天。两只猫的凝集效价都相对较弱(1:1 至 1:8)。主要免疫球蛋白类别是 IgM。
将 FEA1 阴性、初次输血的猫输注 FEA1 阳性血液会导致输血后 5 天内产生抗 FEA1 同种抗体。我们的结果证实了 FEA1 的潜在免疫原性,并支持即使是初次输血的猫在输血前进行交叉配血。需要进一步的研究来更好地记录这些输血后抗体的临床重要性,并促进猫 FEA1 抗原的常规血型鉴定。