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人乳腺腺癌中血浆在蛋白A柱上的体外灌注。蛋白A的Fc结合能力在副作用和杀肿瘤反应中的作用。

Ex vivo perfusion of plasma over protein A columns in human mammary adenocarcinoma. Role of the Fc-binding capacity of protein A in the side effects and the tumoricidal response.

作者信息

Kinet J P, Bensinger W I, Balland N, Saint-Remy M, Frankenne F, Hennen G, Mahieu P

出版信息

Eur J Clin Invest. 1986 Feb;16(1):50-5. doi: 10.1111/j.1365-2362.1986.tb01307.x.

Abstract

Plasma of twelve patients presenting with a metastic mammary adenocarcinoma was perfused ex vivo over columns of protein A covalently linked to crystalline silica. The plasma of seven patients (group A) was perfused over columns of protein A exhibiting a normal Fc-binding capacity and the plasma of five (group B) over columns of protein A in which the Fc-binding capacity was destroyed. In group A, all patients experienced acute, easily manageable, side effects (hypotension, chills, mild fever, leucocytosis and pain in tumour sites) during or immediately after the immunoadsorption procedures, and three exhibited an objective partial regression after two to five sessions. In contrast, none of the patients from group B developed any acute side effects and all showed evident progression of their disease during the treatment. Tumour cells in all stages of destruction, sometimes surrounded by extensive fibrosis, were seen in biopsies of patients A. However, focal areas of active tumour proliferation were always present in these patients. These data confirm that ex vivo perfusion over protein A columns of plasma from patients with cancer can induce a tumoricidal response in some instances and show that the Fc-binding capacity of protein A is most probably responsible for the necrolytic response and the side effects.

摘要

将12例转移性乳腺腺癌患者的血浆在体外灌注到与结晶二氧化硅共价连接的蛋白A柱上。7例患者(A组)的血浆灌注到具有正常Fc结合能力的蛋白A柱上,5例患者(B组)的血浆灌注到Fc结合能力已被破坏的蛋白A柱上。在A组中,所有患者在免疫吸附过程中或之后立即出现急性、易于控制的副作用(低血压、寒战、轻度发热、白细胞增多和肿瘤部位疼痛),3例患者在两到五个疗程后出现客观的部分缓解。相比之下,B组患者均未出现任何急性副作用,且在治疗期间均显示疾病明显进展。在A组患者的活检中可见处于各个破坏阶段的肿瘤细胞,有时被广泛的纤维化包围。然而,这些患者中始终存在活跃肿瘤增殖的局灶区域。这些数据证实,癌症患者血浆在蛋白A柱上进行体外灌注在某些情况下可诱导杀肿瘤反应,并表明蛋白A的Fc结合能力很可能是坏死溶解反应和副作用的原因。

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