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急性髓性白血病血清的蛋白A吸附可诱导体外原始细胞溶解。

Protein A adsorption of acute myelogenous leukemia serum induces in vitro blast lysis.

作者信息

Miller W J, Branda R F, Hurd D D, Wachsman W, Nelson N L, Jacob H S

出版信息

Blood. 1982 Jun;59(6):1344-7.

PMID:7044448
Abstract

We studied cytotoxic activity of acute myelogenous leukemia (AML) sera for AML blasts before and after immunoadsorption with Staphylococcus aureus, Cowan I (SAC), which contains protein A. We found in vitro that incubation with treated AML sera reduced viability to 42.7% of control (p less than 0.01) for autologous and 21.0% of control (p less than 0.01) for allogeneic blasts. Normal peripheral blood cells were not killed by treated AML sera. Wood 46 strain of Staphylococcus aureus, which does not contain protein A, did not significantly reduce AML blast viability (94.8%, p greater than 0.4), while Sepharose-bound protein A reduced viability to 63.8% (p less than 0.01). Cytotoxicity does not appear to be complement-mediated, byt cytotoxic activity is trypsin-sensitive and is contained in the immunoglobulin fraction. This model for study of the tumoricidal action of protein A adsorption should be useful for predicting utility of plasma adsorption as a therapeutic adjunct in the future.

摘要

我们研究了急性髓性白血病(AML)血清对金黄色葡萄球菌Cowan I(SAC,含蛋白A)免疫吸附前后AML原始细胞的细胞毒性活性。我们发现,体外实验中,用处理后的AML血清孵育后,自体原始细胞的活力降至对照的42.7%(p<0.01),同种异体原始细胞的活力降至对照的21.0%(p<0.01)。正常外周血细胞未被处理后的AML血清杀死。不含蛋白A的金黄色葡萄球菌Wood 46菌株未显著降低AML原始细胞活力(94.8%,p>0.4),而琼脂糖结合的蛋白A使活力降至63.8%(p<0.01)。细胞毒性似乎不是补体介导的,但细胞毒性活性对胰蛋白酶敏感且存在于免疫球蛋白组分中。这种用于研究蛋白A吸附的杀肿瘤作用的模型,对于预测血浆吸附作为未来治疗辅助手段的效用应该是有用的。

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