Segel George B, Lichtman Marshall A
Department of Pediatrics, University of Rochester Medical Center, 601 Elmwood Avenue, Rochester, NY 14642-0001, USA; Department of Medicine, 601 Elmwood Avenue, Rochester, NY 14642-0001, USA.
Department of Medicine, 601 Elmwood Avenue, Rochester, NY 14642-0001, USA.
Blood Cells Mol Dis. 2014 Apr;52(4):152-60. doi: 10.1016/j.bcmd.2013.12.003. Epub 2014 Jan 9.
We have reviewed the literature to identify and characterize reports of warm-antibody type, autoimmune hemolytic anemia in which the standard direct antiglobulin reaction was negative but a confirmatory test indicated that the red cells were opsonized with antibody. Three principal reasons account for the absence of a positive direct antiglobulin test in these cases: a) IgG sensitization below the threshold of detection by the commercial antiglobulin reagent, b) low affinity IgG, removed by preparatory washes not conducted at 4°C or at low ionic strength, and c) red cell sensitization by IgA alone, or rarely (monomeric) IgM alone, but not accompanied by complement fixation, and thus not detectable by a commercial antiglobulin reagent that contains anti-IgG and anti-C3. In cases in which the phenotype is compatible with warm-antibody type, autoimmune hemolytic anemia and the direct antiglobulin test is negative, an alternative method to detect low levels of IgG sensitization, use of 4°C, low ionic strength washes to prepare the cells for the direct antiglobulin test reaction to permit retention and identification of low affinity IgG antibodies, and, if the latter are uninformative, testing for sensitization with an anti-IgA, and, if necessary, an anti-IgM reagent identifies cases of warm-antibody type, immune hemolysis not verified by a commercial reagent.
我们查阅了文献,以识别和描述温抗体型自身免疫性溶血性贫血的报告,其中标准直接抗球蛋白试验为阴性,但确证试验表明红细胞被抗体调理。这些病例中直接抗球蛋白试验呈阴性主要有三个原因:a)IgG致敏低于商业抗球蛋白试剂的检测阈值;b)低亲和力IgG,在非4°C或低离子强度下进行的预备洗涤中被去除;c)仅由IgA或极少情况下(单体)仅由IgM引起的红细胞致敏,但不伴有补体固定,因此含有抗IgG和抗C3的商业抗球蛋白试剂无法检测到。在表型与温抗体型自身免疫性溶血性贫血相符且直接抗球蛋白试验为阴性的病例中,检测低水平IgG致敏的替代方法是使用4°C、低离子强度洗涤来制备细胞用于直接抗球蛋白试验反应,以保留和鉴定低亲和力IgG抗体,如果后者无信息价值,则用抗IgA检测致敏情况,如有必要,用抗IgM试剂检测,可识别出商业试剂未证实的温抗体型免疫性溶血病例。