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白细胞透析液和胸腺素对胰蛋白酶处理的人淋巴细胞中绵羊细胞玫瑰花结形成能力恢复的双重作用。

Dual action of leucocyte dialysates and of thymosin on the recovery of sheep-cell-rosetting capacity in trypsinized human lymphocytes.

作者信息

Sargent I L, Salaman M R, Valdimarsson H

出版信息

Clin Exp Immunol. 1982 Jan;47(1):183-90.

Abstract

Trypsinization of human blood lymphocytes abolishes their capacity to form rosettes with sheep erythrocytes (E-rosettes) and this is regained in part on incubation of the cells at 37 degrees C for 3 hr. The recovery of rosetting capacity was found to be accelerated in the presence of dialysable extracts of human leucocytes (DLE) or bovine thymosin fraction 5 (THFV). For both DLE and THFV two types of effect were demonstrated. At lower concentrations the stimulation of recovery was dependent on the presence of the agent during incubation and it presumably comes about through an effect on the metabolic process required for regeneration of the E-receptors. At higher concentrations another mechanism is apparent since the agents were now effective when added after incubation. This last phenomenon is wholly dependent on prior incubation of the trypsinized lymphocytes in medium alone and it probably involves attachment of components of DLE and THFV to incompletely recovered cells, thereby providing a more favourable charge environment for E-rosette formation. A similar process of adhesion-promotion may be occurring in certain in-vitro tests with THFV which are carried out on lymphocytes from immunodeficient patients. On the other hand, it is the other mechanism, that of metabolic action, which is likely to be the predominant consideration in relation to treatment of such patients with DLE or THFV.

摘要

人血淋巴细胞经胰蛋白酶处理后,会丧失与绵羊红细胞形成花环(E花环)的能力,而将细胞在37℃孵育3小时后,这种能力会部分恢复。发现在存在人白细胞透析提取物(DLE)或牛胸腺素组分5(THFV)的情况下,花环形成能力的恢复会加速。对于DLE和THFV,都证明了两种类型的作用。在较低浓度下,恢复的刺激取决于孵育期间试剂的存在,推测这是通过对E受体再生所需的代谢过程产生影响而实现的。在较高浓度下,另一种机制很明显,因为这些试剂在孵育后添加时现在是有效的。最后这种现象完全取决于仅在培养基中对经胰蛋白酶处理的淋巴细胞进行预先孵育,并且它可能涉及DLE和THFV的成分附着于未完全恢复的细胞,从而为E花环形成提供更有利的电荷环境。在对免疫缺陷患者的淋巴细胞进行的某些使用THFV的体外试验中,可能正在发生类似的促进黏附过程。另一方面,在考虑用DLE或THFV治疗此类患者时,可能主要考虑的是另一种机制,即代谢作用机制。

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