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血清诱导系统性硬化症患者外周血单个核细胞对人靶细胞细胞毒性的增强。

Serum-induced enhancement of peripheral blood mononuclear cell-mediated cytotoxicity towards human target cells in systemic sclerosis.

作者信息

Penning C A, Wright J K, Ashby J C, Cunningham J, Rowell N R, Hughes P

出版信息

J Clin Lab Immunol. 1983 Oct;12(2):77-81.

PMID:6644792
Abstract

Sera from 7 of 37 patients with systemic sclerosis (SS) were found to markedly enhance cytotoxicity in several established human target cell lines when co-cultured with normal human peripheral blood mononuclear cells (PBM). Fractionation studies indicated that the cytotoxicity-inducing activity resided in the IgG-containing fractions of serum and that the effector cells were Fc-receptor positive. By contrast, sera from 27 normal controls produced little or no cytotoxicity when co-cultured with the same target cell lines and normal PBM. Any slight enhancement of cytotoxicity that occurred with a single target cell line was, on fractionation, either labile or associated with albumin containing fractions. These findings raise the possibility that antibody-dependent cellular cytotoxicity (ADCC) could provide a pathogenetic mechanism in some patients with SS.

摘要

在37例系统性硬化症(SS)患者中,发现7例患者的血清在与正常人外周血单个核细胞(PBM)共培养时,能显著增强几种已建立的人靶细胞系的细胞毒性。分级分离研究表明,细胞毒性诱导活性存在于血清中含IgG的组分中,效应细胞为Fc受体阳性。相比之下,27例正常对照的血清在与相同靶细胞系和正常PBM共培养时,产生的细胞毒性很小或没有。对于单个靶细胞系出现的任何轻微细胞毒性增强,经分级分离后,要么不稳定,要么与含白蛋白的组分有关。这些发现增加了抗体依赖性细胞毒性(ADCC)可能为某些SS患者提供发病机制的可能性。

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