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Folia haematologica (Leipzig, Germany : 1928)最新文献

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[Effect of ultraviolet light on the UV/VIS absorption spectrum of components of Eagle (MEM) cell culture medium]. [紫外光对Eagle (MEM)细胞培养基成分紫外/可见吸收光谱的影响]。
G Bollmann, K Redmann

The impact of ultraviolet light on uv/vis absorption spectra of selected individual components of the cell breeding medium according to Eagle (MEM) was investigated. The strongest alterations of light absorption were detected in L-phenylalanine, L-tyrosine and L-tryptophan. Thus, the absorption behaviour of the Eagle (MEM) medium changed post radiation may be attributed to spectrophotometric alterations of absorption in aromatic amino acids. The results are discussed with regard to the effect on the surface charge of erythrocytes.

根据Eagle (MEM)研究了紫外光对细胞培养培养基中各组分紫外/可见吸收光谱的影响。l -苯丙氨酸、l -酪氨酸和l -色氨酸的光吸收变化最大。因此,辐射后Eagle (MEM)介质的吸收行为变化可能归因于对芳香氨基酸吸收的分光光度变化。讨论了对红细胞表面电荷的影响。
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引用次数: 0
Striking feature of alpha-fetoprotein (AFP): stimulation of the phagocytic capabilities of human blood platelets. 甲胎蛋白(AFP)的显著特征:刺激人血小板的吞噬能力。
H Kemona, M Czokało, M Mantur, J Prokopowicz

In concentrations from 2.5 x 10(3) to 480 x 10(3) ng/ml AFP is able to increase the phagocytic index and the phagocytizing percentage of human blood platelets in vitro conditions. This effect is dependent on the dose of AFP and time of incubation.

在2.5 × 10(3)至480 × 10(3) ng/ml浓度范围内,甲胎蛋白能够增加体外条件下人血小板的吞噬指数和吞噬百分率。这种效果取决于甲胎蛋白的剂量和孵育时间。
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引用次数: 0
[Thrombocytopenia after autologous bone marrow transplantation in in acute lymphatic leukemia]. 急性淋巴白血病自体骨髓移植后血小板减少的研究。
E Siegert, I Lauterbach, G Weissbach

There is reported about the treatment of refractory thrombocytopenia in a 9 years old boy following the autologous bone marrow transplantation for acute lymphoblastic leukaemia. The megakaryocytes were found diminished in the bone marrow smears. Controls of the thrombocyte count and the kinetics with radioactively labeled platelets of a donor spoke in favour of immunothrombocytopenia. Threatening bleeding complications challenged the use of all treatment possibilities. The irradiation of the spleen was without any success. After the splenectomy the thrombocyte count increased slowly, but after a remarkable lag phase, however. A diminished reproduction capacity of the bone marrow graft for special cell sorts has to be taken into account in such cases. The usual cytodynamics after splenectomy cannot be expected at all.

报道一例9岁男童急性淋巴细胞白血病行自体骨髓移植后难治性血小板减少症的治疗。骨髓涂片显示巨核细胞减少。控制血小板计数和动力学与供体放射性标记血小板有利于免疫血小板减少。危险的出血并发症挑战了所有治疗方法的使用。脾脏的照射没有成功。脾切除术后血小板计数增加缓慢,但有明显的滞后期。在这种情况下,必须考虑到特殊细胞种类的骨髓移植物的繁殖能力下降。脾切除术后通常的细胞动力学完全不能预料。
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引用次数: 0
Inhibitor of granulopoiesis in human cyclic neutropenia. 人循环中性粒细胞减少症的颗粒生成抑制剂。
V Cukrová, H Klamová

Peripheral blood mononuclear cells of a patient with cyclic neutropenia release a high molecular weight substance (over 300,000) inhibiting normal CFU-GM cells to enter the S-phase of cell cycle. The inhibitor was released predominantly in the neutropenic phase of the disease, while in the period of normal granulocyte count the release was lower or undetectable. Also sensitivity of patient's bone marrow CFU-GM cells to similar high molecular weight inhibitor produced by ML-2 cell liner or to human placental ferritin varied within the disease cycle. CFU-GM in the normal granulocyte count period were sensitive to the inhibitors, but CFU-GM in the neutropenic phase were resistant.

循环中性粒细胞减少症患者外周血单核细胞释放高分子量物质(超过300,000),抑制正常CFU-GM细胞进入细胞周期s期。该抑制剂主要在疾病的中性粒细胞减少期释放,而在粒细胞计数正常期间释放较低或无法检测到。此外,患者骨髓CFU-GM细胞对ML-2细胞系产生的类似的高分子量抑制剂或对人胎盘铁蛋白的敏感性在疾病周期内也有所不同。正常粒细胞计数期CFU-GM对抑制剂敏感,中性粒细胞减少期CFU-GM耐药。
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引用次数: 0
[Malondialdehyde formation by platelets of hemophiliacs]. 血友病患者血小板中丙二醛的形成。
B Maak, F Marrouchieh

The platelets of haemophilic patients produce after stimulation with thrombin (5 NIH-units) a significantly reduced amount of malondialdehyde in comparison to the platelets of healthy children of the same age. There is a positive correlation between the platelet count in citrated whole blood and malondialdehyde production in the group of healthy children, however the same correlation is negative in adults and strongly negative in haemophiliacs. Because of the 24 hour-intervals between the last substitution and investigation in the majority of haemophilic patients, the reduced MDA-production of their platelets seems to be the result of side effects of the administration of plasma fractions. On the other hand, the reduced capacity for the MDA-production of the platelets of haemophiliacs can be explained as the result of the release reaction of platelets after haemostasis activation following bleedings.

与同龄健康儿童的血小板相比,血友病患者的血小板在凝血酶(5 nih单位)刺激后产生的丙二醛显著减少。在健康儿童中,柠檬酸全血血小板计数与丙二醛生成呈正相关,但在成人中呈负相关,在血友病患者中呈强负相关。由于在大多数血友病患者中,在最后一次替代和调查之间有24小时的间隔,其血小板mda生成的减少似乎是给药血浆组分的副作用的结果。另一方面,血友病患者血小板产生mda的能力降低可以解释为出血后止血激活后血小板释放反应的结果。
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引用次数: 0
Granulocytopoiesis in children with acute lymphoblastic leukaemia. 急性淋巴细胞白血病患儿的粒细胞生成。
E B Vladimirskaya, N S Shersheneva, S Sallam, N V Zamaraeva, S N Chukanin

Numbers, proliferative potential, and differentiative capacity of bone marrow granulocyte-macrophage precursor cells were studied in 130 children with acute lymphoblastic leukaemia (ALL), including 77 children in an acute phase of the disease and 53 in remission. Bone marrow samples from 65 children without haematopoietic abnormalities were used as controls. The numbers of clonogenic precursors were found to be below normal in all phases of ALL, particularly during the acute period when the bone marrow was heavily infiltrated with leukaemic cells. It is shown that the decreases in the numbers and proliferative potential of the precursor cells during the acute phases was associated with the effects of leukaemic blast cells, but that in remission the observed reduction in the precursor cell pool was due to the cytostatic effect of therapy. The differentiative capacity of clonogenic granulocyte and macrophage precursors was not altered in children with ALL.

研究了130例急性淋巴细胞白血病(ALL)患儿骨髓粒细胞-巨噬细胞前体细胞的数量、增殖潜能和分化能力,包括77例急性期患儿和53例缓解期患儿。65例无造血异常儿童的骨髓样本作为对照。在急性淋巴细胞白血病的所有阶段,克隆前体细胞的数量都低于正常水平,特别是在骨髓被白血病细胞严重浸润的急性期。研究表明,在急性期,前体细胞数量和增殖潜力的减少与白血病母细胞的作用有关,但在缓解期,观察到的前体细胞池的减少是由于治疗的细胞抑制作用。ALL患儿克隆原性粒细胞和巨噬细胞前体的分化能力未发生改变。
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引用次数: 0
[Are our blood donors in danger of iron deficiency?]. 献血者是否有缺铁的危险?
L H Schmidt, W Gulich

In blood donors the question arises for eventual endangering by iron deficiency. The results of this work show that ferritin determinations for blood donors will indicate a latent, in some cases a manifest iron deficiency. The examination of testing components such as PVC, MCH, Fe i. S., transferrin and transferrin saturation produced no special advantages concerning sensitivity and specificity, in terms of ferritin determination. It is indispensable, however, to know the ferritin value because the control of the Hb value prior to blood donation will usually characterize the blood donor's situation in a sufficient manner. For control purposes it is possible to use capillary or venous blood. It is only in general, but particularly in special clinical situations that you have to be aware of the blood donor's condition concerning his/her Fe-metabolism.

对于献血者来说,缺铁可能会危及生命。这项工作的结果表明,对献血者的铁蛋白测定将表明潜在的,在某些情况下明显缺铁。在铁蛋白测定方面,检测成分如PVC、MCH、Fe . S、转铁蛋白和转铁蛋白饱和度在敏感性和特异性方面没有特别的优势。然而,了解铁蛋白值是必不可少的,因为献血前Hb值的控制通常可以充分表征献血者的情况。为了控制目的,可以使用毛细血管或静脉血。只有在一般情况下,特别是在特殊的临床情况下,你必须了解献血者的铁代谢状况。
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引用次数: 0
[4th Haemophilia symposium of the German Democratic Republic with international participation. Dresden, 22-25 November 1989]. 第四届德意志民主共和国血友病国际研讨会。德累斯顿,1989年11月22-25日]。
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引用次数: 0
[Antibodies to anticoagulants in rheumatic autoimmune diseases]. [风湿病自身免疫性疾病的抗凝血抗体]。
E Gromnica-Ihle, W Schössler, J Franz, S Ziemer, H Hüge, E Apostoloff

The systemic lupus erythematosus (SLE) and the rheumatoid arthritis (RA) as the classic autoimmune diseases exhibit a great number of autoantibodies. Some of them are anticoagulants. Besides inactivating inhibitors against single coagulation factors interfering anticoagulants are known, belonging to the group of anti-phospholipid antibodies and detected as the lupus anticoagulants or anticardiolipin antibodies. Anti-phospholipid antibodies 184 patients with SLE or RA had been checked for. An enzyme immuno assay was used for detection of the anti-cardiolipin antibodies. The relations between occurrence of the anti-cardiolipin antibodies and vascular processes as well as other immunologic parameters had been tested for clinical relevancy.

系统性红斑狼疮(SLE)和类风湿性关节炎(RA)是典型的自身免疫性疾病,具有大量自身抗体。有些是抗凝血剂。除已知的抗单一凝血因子的失活抑制剂外,还属于抗磷脂抗体的范畴,被检测为狼疮抗凝血剂或抗心磷脂抗体。184例SLE或RA患者进行了抗磷脂抗体检测。采用酶免疫法检测抗心磷脂抗体。抗心磷脂抗体的发生与血管进程以及其他免疫学参数之间的关系已被测试临床相关性。
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引用次数: 0
Evaluation of wet pasteurization of a factor VIII concentrate produced by controlled-pore silica adsorption. 控制孔二氧化硅吸附生产的因子VIII浓缩物的湿法巴氏灭菌评价。
H Hiemstra, C E Nieuweboer, M A Idoe, J E Claassen, A H Vos, M Tersmette, P F Strengers, J Over, E P Mauser-Bunschoten, H Heijboer

In the routine production of a factor VIII concentrate (produced by adsorption of contaminating proteins in cryoprecipitate to controlled-pore silica and concentration of the factor VIII effluent by ultrafiltration) the terminal dry-heat treatment has been replaced by pasteurization in the liquid state. High effectivity of this procedure with respect to virus inactivation was demonstrated using a variety of both lipid- and protein-enveloped model viruses, including HIV. Pair-wise quality control of dry-heated and pasteurized product revealed no significant differences, except in the composition of the formulation buffer. In a clinical study in which 17 patients with haemophilia A participated the pasteurized product was well tolerated and in vivo recovery and half-life of factor VIII were in the same (normal) range as found for the dry-heated counterpart.

在因子VIII浓缩物的常规生产中(通过将冷冻沉淀中的污染蛋白质吸附到控制孔二氧化硅上并通过超滤浓缩因子VIII流出物而生产),末端干热处理已被液态巴氏灭菌所取代。使用包括HIV在内的多种脂质和蛋白质包膜模型病毒,证明了该程序在病毒失活方面的高效性。干加热和巴氏灭菌产品的成对质量控制显示,除了配方缓冲液的组成外,没有显着差异。在一项有17名a型血友病患者参与的临床研究中,巴氏灭菌产品耐受性良好,体内恢复和因子VIII的半衰期与干热产品相同(正常)。
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Folia haematologica (Leipzig, Germany : 1928)
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