Faille A, Barrett A J, Balitrand N, Ketels F, Gluckman E, Najean Y
Br J Haematol. 1979 Jul;42(3):371-80. doi: 10.1111/j.1365-2141.1979.tb01145.x.
Granylocyte colony forming units (CFU-C) were studied in 22 patients with severe aplastic anaemia before and after treatment with antilymphocyte globulin (ALG). Nine patients showed a clinical response to ALG characterized by a rise in the granulocyte count to over I X 10(9)/1 within 30 d. These patients were distinguished in vitro from non-responders by an increase in CFU-C numbers after incubation of bone marrow cells with ALG, and by the presence of inhibitors of normal CFU-C in the serum in six out of seven patients tested. In responding patients bone marrow CFU-C rose while most non-responding patients showed no change or a fall in CFU-C after treatment. In addition in three out of four responding patients examined serum inhibitors disappeared after treatment. The horse ALG used in this study also stimulated normal CFU-C in vitro. This evidence is contrary to the hypothesis that ALG stimulates CFU-C in aplasia by inactivating an abnormal suppressor lymphocyte population. The nature of the stimulation by ALG remains unclear. But in practice the effect of ALG on bone marrow cells and study of CFU-C inhibitors in serum could be used to select patients likely to respond to ALG treatment.
对22例重型再生障碍性贫血患者在使用抗淋巴细胞球蛋白(ALG)治疗前后进行了粒细胞集落形成单位(CFU-C)的研究。9例患者对ALG有临床反应,表现为粒细胞计数在30天内升至超过1×10⁹/L。这些患者在体外与无反应者的区别在于,骨髓细胞与ALG孵育后CFU-C数量增加,且在7例检测患者中有6例血清中存在正常CFU-C的抑制剂。有反应的患者骨髓CFU-C升高,而大多数无反应的患者治疗后CFU-C无变化或下降。此外,在4例接受检查的有反应患者中有3例治疗后血清抑制剂消失。本研究中使用的马ALG在体外也能刺激正常CFU-C。这一证据与ALG通过使异常抑制性淋巴细胞群体失活来刺激再生障碍性贫血中CFU-C的假说相反。ALG刺激的本质尚不清楚。但在实际应用中,ALG对骨髓细胞的作用以及血清中CFU-C抑制剂的研究可用于选择可能对ALG治疗有反应的患者。