Cohen D W, Garratty G, Morel P, Petz L D
Transfusion. 1979 May-Jun;19(3):329-31. doi: 10.1046/j.1537-2995.1979.19379204217.x.
A second case of autoimmune hemolytic anemia mediated by an IgG auto Anti-N is described. The patient's red blood cells were sensitized with both IgG and complement. The serum antibody was not inactivated by 2-mercaptoethanol treatment, and reacted by indirect antiglobulin test at 37 C with monospecific anti-IgG. The IgG antibody eluted from the red blood cells and in the serum showed anti-N specificity. The patient was thought to have systemic lupus erythematosus. Following steroid therapy, the hemolytic anemia resolved with disappearance of the anti-N.
本文描述了第二例由IgG自身抗-N介导的自身免疫性溶血性贫血病例。患者的红细胞被IgG和补体致敏。血清抗体经2-巯基乙醇处理后未失活,并在37℃通过间接抗球蛋白试验与单特异性抗IgG发生反应。从红细胞洗脱的IgG抗体以及血清中的IgG抗体均显示抗-N特异性。该患者被认为患有系统性红斑狼疮。经过类固醇治疗后,溶血性贫血得以缓解,抗-N消失。