Groshong T, Horowitz S, Lovchik J, Davis A, Hong R
J Pediatr. 1976 Feb;88(2):217-23. doi: 10.1016/s0022-3476(76)80985-7.
An infant with severe combined immunodeficiency had normal numbers of lymphocytes which bore E rosette and surface Ig markers in an appropriate distribution. However, only minimal responsivity to in vitro stimulation by mitogens and allogenic cells, and none to antigens could be elicited; functional antibody responses were also nil, except to cytomegalovirus. Intrauterine-acquired cytomegalovirus may have caused his immune dysfunction, although the possibility of a postnatal infection cannot be excluded. Therapy with transfer factor and thymus transplantation was unsucessful in restoring immunity and may have aggravated a pre-existing monoclonal gammopathy. It is possible that the monoclonal protein was derived from B-cells transplacentally received from the patients mother.
一名患有严重联合免疫缺陷的婴儿,其淋巴细胞数量正常,这些淋巴细胞带有E花环和表面免疫球蛋白标记,且分布适当。然而,对有丝分裂原和同种异体细胞的体外刺激仅产生最小反应,对抗原则无反应;除了对巨细胞病毒外,功能性抗体反应也为零。宫内获得的巨细胞病毒可能导致了他的免疫功能障碍,尽管不能排除产后感染的可能性。用转移因子和胸腺移植进行治疗未能成功恢复免疫功能,且可能加重了原有的单克隆丙种球蛋白病。单克隆蛋白有可能来源于经胎盘从患儿母亲获得的B细胞。