Bordigoni P, Faure G, Bene M C, Dardenne M, Bach J F, Duheille J, Olive D
Lancet. 1982 Aug 7;2(8293):293-7. doi: 10.1016/s0140-6736(82)90271-9.
Three children with IgA and IgE deficiency and T-cell defects (two related patients with ataxia telangiectasia and one with common variable immune deficiency) were treated with synthetic serum thymic factor (FTS) intravenously. A reduction in frequency and severity of infection was noted concomitantly with improvement in cell-mediated-immunity tests. Serum IgA, which was absent in two patients, appeared within 4 weeks of treatment and increased significantly in the third patient. Specific antibodies against vaccination antigens appeared for the first time or increased to titres higher than ever before. In two patients, transient interruption of FTS administration was followed by a regression of the immunological improvement, but this disappeared after the treatment was started again.
三名患有IgA和IgE缺乏以及T细胞缺陷的儿童(两名共济失调毛细血管扩张症相关患者和一名普通可变免疫缺陷患者)接受了静脉注射合成血清胸腺因子(FTS)治疗。观察到感染频率和严重程度降低,同时细胞介导免疫测试有所改善。两名患者原本缺乏的血清IgA在治疗4周内出现,第三名患者的血清IgA显著增加。针对疫苗接种抗原的特异性抗体首次出现或升至前所未有的滴度。在两名患者中,短暂中断FTS给药后免疫改善情况出现倒退,但再次开始治疗后这种情况消失了。