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重型地中海贫血中的中性粒细胞功能障碍:细胞铁过载的作用。

Neutrophil dysfunctions in thalassaemia major: the role of cell iron overload.

作者信息

Cantinieaux B, Hariga C, Ferster A, De Maertelaere E, Toppet M, Fondu P

机构信息

Department of Haematology, Hospital St. Pierre, Free University of Brussels, Belgium.

出版信息

Eur J Haematol. 1987 Jul;39(1):28-34. doi: 10.1111/j.1600-0609.1987.tb00159.x.

Abstract

The susceptibility to infections was recorded in 13 patients with beta thalassaemia major (T.P.). The following parameters were also investigated in their polymorphonuclear neutrophils (PMN): nitro blue tetrazolium (NBT) reduction, heated yeast and Escherichia coli phagocytosis, Escherichia coli killing and myeloperoxydase activity. These results were compared to those obtained in healthy controls (H.C.). The Perls's reaction was performed on PMN and graded according to a scoring system with the aim of quantifying the iron intoxication of PMN. Phagocytosis and Perls's reaction of PMN from H.C. were also studied after 20 h of incubation with thalassaemic serum. 6 T.P. out of 13 developed septicaemia during their lifetime and in all 9 septicaemic episodes were noted. Phagocytosis was greatly impaired, disclosing both cellular and serum abnormalities. The mean percentage of Perls's positive PMN was 13% in T.P., contrasting with the constant negative reaction in H.C. The incubation of PMN from H.C. with serum from T.P. induced the simultaneous appearance of a phagocytosis defect and of a positive Perl's reaction. It was concluded that in beta thalassaemia major the phagocytosis of PMN was altered due to a combination of serum and cellular abnormalities and that both may be related to the iron overload.

摘要

记录了13例重型β地中海贫血(T.P.)患者的感染易感性。还对其多形核中性粒细胞(PMN)的以下参数进行了研究:硝基蓝四氮唑(NBT)还原、加热酵母和大肠杆菌吞噬作用、大肠杆菌杀伤及髓过氧化物酶活性。将这些结果与健康对照(H.C.)所得结果进行比较。对PMN进行了派尔反应,并根据评分系统进行分级,目的是量化PMN的铁中毒情况。在与地中海贫血血清孵育20小时后,还研究了来自H.C.的PMN的吞噬作用和派尔反应。13例T.P.中有6例在其一生中发生了败血症,共记录到9次败血症发作。吞噬作用严重受损,显示出细胞和血清异常。T.P.中派尔阳性PMN的平均百分比为13%,而H.C.中反应始终为阴性。来自H.C.的PMN与来自T.P.的血清孵育导致吞噬缺陷和派尔反应阳性同时出现。得出的结论是,在重型β地中海贫血中,PMN的吞噬作用因血清和细胞异常的共同作用而改变,且两者可能都与铁过载有关。

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