Szymanski I O, Huff S R, Selbovitz L G, Sherwood G K
Am J Hematol. 1984 Jul;17(1):71-7. doi: 10.1002/ajh.2830170109.
An automated antiglobulin test showed that erythrocytes of a patient with an acute episode of Coombs-negative hemolytic anemia were strongly sensitized with nonagglutinating IgM molecules. The bound antibodies, after elution from red blood cell stroma, were found to be monomeric IgM, since they migrated with IgG molecules on an agarose column, although they were proved to be immunoglobulin M, not G, by a sensitive hemagglutination inhibition assay. The hemolysis subsided with steroid therapy, but ANA increased to a titer greater than 1,024 (with peripheral pattern) without other laboratory evidence of systemic lupus erythematosus. In addition, the patient demonstrated photosensitivity and nonscarring alopecia. We consider that this appearance of erythrocyte autoantibodies consisting of monomeric IgM was a symptom of atypical SLE.
一项自动抗球蛋白试验显示,一名患有急性库姆斯阴性溶血性贫血发作的患者的红细胞被非凝集性IgM分子强烈致敏。从红细胞基质洗脱后,发现结合的抗体为单体IgM,因为它们在琼脂糖柱上与IgG分子一起迁移,尽管通过灵敏的血凝抑制试验证明它们是免疫球蛋白M而非G。溶血通过类固醇治疗消退,但抗核抗体升高至大于1024的滴度(周边型),且无其他系统性红斑狼疮的实验室证据。此外,该患者表现出光敏性和非瘢痕性脱发。我们认为这种由单体IgM组成的红细胞自身抗体的出现是非典型系统性红斑狼疮的一种症状。