Aiuti F, Businco L, Fiorilli M, Galli E, Quinti I, Rossi P, Seminara R, Goldstein G
Lancet. 1983 Mar 12;1(8324):551-4. doi: 10.1016/s0140-6736(83)92810-6.
26 patients with primary immunodeficiencies (3 infants with severe combined immunodeficiency [SCID] 3 with DiGeorge syndrome, 6 with T-cell defect or SCID with B cells, 4 with common variable hypogammaglobulinaemia and associated T-cell defect, 5 with ataxia-telangiectasia, and 5 with hyper-IgE syndrome) were treated with thymopoietin pentapeptide (TP-5) at a dose of 0 . 5 mg/kg daily for 2 weeks and then 3 times a week at 0 . 5 mg/kg for 10 weeks, 3 patients with DiGeorge syndrome and 3 with primary T-cell defect demonstrated pronounced clinical and immunological improvement during treatment. None of the patients with SCID and 3 of 6 patients with SCID with B cells or primary T-cell defect showed any clinical or immunological changes during therapy. In 5 patients with ataxia-telangiectasia clinical manifestations and immunological tests were unchanged by TP-5. Abnormality of T cells in cases of hyper-IgE syndrome was not corrected by TP-5 treatment.
26例原发性免疫缺陷患者(3例严重联合免疫缺陷[SCID]婴儿、3例迪格奥尔格综合征患者、6例T细胞缺陷或伴有B细胞的SCID患者、4例常见变异型低丙种球蛋白血症及相关T细胞缺陷患者、5例共济失调-毛细血管扩张症患者和5例高IgE综合征患者)接受胸腺生成素五肽(TP-5)治疗,剂量为每日0.5mg/kg,持续2周,然后每周3次,每次0.5mg/kg,共10周。3例迪格奥尔格综合征患者和3例原发性T细胞缺陷患者在治疗期间表现出明显的临床和免疫学改善。SCID患者无一例以及6例伴有B细胞或原发性T细胞缺陷的SCID患者中有3例在治疗期间未出现任何临床或免疫学变化。5例共济失调-毛细血管扩张症患者的临床表现和免疫检查未因TP-5而改变。高IgE综合征患者的T细胞异常未通过TP-5治疗得到纠正。