Gelfand E W, Parkman R, Rosen F S
Birth Defects Orig Artic Ser. 1975;11(1):158-62.
A 14-year-old boy with a lifelong history of recurrnet infections and debilitating bronchiectasis was found to lack any evidence of humoral or cellular immunity. His serum contained a high titer of IgM antibody to the heavy chain of IgG and this antibody was also cytotoxic for peripheral lymphocytes. Complement-dependent lymphocytotoxicity could be blocked by IgG or Fc fragment. In this patient, immunosuppression may have been due to an autoantibody against both autologous IgG and lymphocyte plasma membrane.
一名患有复发性感染和使人虚弱的支气管扩张症的14岁男孩被发现缺乏体液免疫或细胞免疫的任何证据。他的血清中含有高滴度的针对IgG重链的IgM抗体,并且这种抗体对外周淋巴细胞也具有细胞毒性。补体依赖性淋巴细胞毒性可被IgG或Fc片段阻断。在该患者中,免疫抑制可能是由于针对自身IgG和淋巴细胞质膜的自身抗体所致。