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急性非淋巴细胞白血病中的α2抗纤溶酶

Alpha-2 antiplasmin in acute nonlymphoblastic leukemia.

作者信息

Cofrancesco E, Pogliani E, Salvatore M, Moreo G, Boschetti C, Cortellaro M

机构信息

Istituto di Scienze Mediche, Università di Milano, Italia.

出版信息

Acta Haematol. 1989;81(3):122-5. doi: 10.1159/000205542.

Abstract

The levels of alpha-2-antiplasmin (alpha 2-AP), antithrombin III (At III) and plasminogen were studied in 21 patients with acute nonlymphoblastic leukemia (ANLL) before and after induction chemotherapy and during bone marrow cellularity recovery after the postchemotherapy aplastic phase. In the patients with M2, M3 or M4 leukemia who had clinical and laboratory evidence of DIC, the alpha 2-AP levels were very low in the initial phase of the disease but improved significantly during recovery of marrow cellularity. At III and plasminogen values were in the normal range at disease onset and showed no significant modification during the course of leukemia. Proteolytic cleavage of alpha 2-AP by granulocyte proteases, rather than hyperfibrinolysis, may be responsible for the low levels of the inhibitor in the proliferative phase of ANLL. This alpha 2-AP deficiency may well contribute to hemorrhagic diathesis in ANLL independently of the presence or absence of hyperfibrinolysis or DIC. Moreover, the lower alpha 2-AP levels observed during the proliferative phase of ANLL may relate to disease activity.

摘要

对21例急性非淋巴细胞白血病(ANLL)患者在诱导化疗前后以及化疗后再生障碍期骨髓细胞恢复期间的α-2-抗纤溶酶(α2-AP)、抗凝血酶III(At III)和纤溶酶原水平进行了研究。在有弥散性血管内凝血(DIC)临床和实验室证据的M2、M3或M4白血病患者中,疾病初始阶段α2-AP水平非常低,但在骨髓细胞恢复期间显著改善。At III和纤溶酶原值在疾病发作时处于正常范围,在白血病病程中无显著变化。ANLL增殖期α2-AP水平降低可能是由于粒细胞蛋白酶对其进行蛋白水解裂解,而非高纤溶状态所致。这种α2-AP缺乏可能独立于高纤溶或DIC的存在与否,导致ANLL患者出现出血素质。此外,ANLL增殖期观察到的较低α2-AP水平可能与疾病活动有关。

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