Ambrus M, Horváth L, Bajtai G, Paál M, Papp T, Kádas I
Folia Haematol Int Mag Klin Morphol Blutforsch. 1977;104(1):39-47.
A 17-year-old girl with humoral immune deficiency state was observed, in whom pernicious anemia developed one year before her death. The patient died after a very severe diarrheal attack and respiratory tract infection. The necropsy revealed intestinal nodular lymphoid hyperplasia. The immunological evaluation showed depressed IgG and IgM concentration with lack of IgA, however in the patient's blood there were found B lymphocytes containing IgA immunoglobulin. On the effect of crude gastric antigen the patient's lymphocytes showed M.I.F. release, although there were no circulating autoantibodies.
观察到一名17岁患体液免疫缺陷状态的女孩,她在死前一年出现了恶性贫血。患者在一次非常严重的腹泻发作和呼吸道感染后死亡。尸检显示肠道结节性淋巴组织增生。免疫学评估显示IgG和IgM浓度降低且缺乏IgA,然而在患者血液中发现了含有IgA免疫球蛋白的B淋巴细胞。尽管没有循环自身抗体,但在粗制胃抗原的作用下,患者的淋巴细胞显示出巨噬细胞移动抑制因子(M.I.F.)释放。