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对刀豆球蛋白A诱导的人体抑制细胞检测法的重新评估。

A reevaluation of the concanavalin A induced suppressor cell assay in man.

作者信息

Knaab S, Jeannet M

出版信息

Int Arch Allergy Appl Immunol. 1983;71(2):97-102. doi: 10.1159/000233370.

Abstract

Several methods are used to evaluate the in vitro suppressor function of human peripheral blood lymphocytes (PBL). Recently however, the validity of these assays has been questioned, because possible artefacts may lead to misinterpretation of the results. A reevaluation of these assays has been performed, and a simple and reproducible technique necessitating only one bleeding has been developed. Pretreatment of human PBL with concanavalin A (ConA) results in an inhibition of 3H-thymidine incorporation after ConA stimulation by cocultured untreated autologous or allogeneic PBL collected at the same time and incubated under the same conditions as the inhibitory PBL. It is concluded that true suppression is responsible for the observed inhibition of the response to ConA and that this assay can be used to assess the functional ability of suppressor cells in different clinical situations.

摘要

有几种方法可用于评估人外周血淋巴细胞(PBL)的体外抑制功能。然而最近,这些检测方法的有效性受到了质疑,因为可能存在的假象可能导致对结果的错误解读。已经对这些检测方法进行了重新评估,并开发出一种仅需一次采血的简单且可重复的技术。用伴刀豆球蛋白A(ConA)对人PBL进行预处理,在受到ConA刺激后,与同时采集并在与抑制性PBL相同条件下孵育的未经处理的自体或异体PBL共培养,会导致3H-胸腺嘧啶核苷掺入受到抑制。得出的结论是,真正的抑制作用是观察到的对ConA反应抑制的原因,并且该检测方法可用于评估不同临床情况下抑制细胞的功能能力。

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