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多克隆启动导致产生白细胞介素4的T细胞频率增加。使用单细胞检测法检测产生白细胞介素4的细胞。

Increased frequency of interleukin 4-producing T cells as a result of polyclonal priming. Use of a single-cell assay to detect interleukin 4-producing cells.

作者信息

Seder R A, Le Gros G, Ben-Sasson S Z, Urban J, Finkelman F D, Paul W E

机构信息

Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892.

出版信息

Eur J Immunol. 1991 May;21(5):1241-7. doi: 10.1002/eji.1830210522.

Abstract

A limiting dilution assay capable of detecting interleukin 4 (IL4) production by a single cell has been developed. This assay is based on the stimulation of T cells, in the presence of IL2 (5 U/ml), with anti-CD3 antibody bound to the surface of Terasaki wells. Cells of the IL4-selective indicator line, CT.4S, are added 24-36 h later and IL4 production is determined based on their survival 24-48 h thereafter. A frequency of 0.98 was obtained for IL4 production by T cells of the D10.G4 cell line. T cells from naive donors capable of producing IL4 in response to anti-CD3 plus IL2 were quite rare, with a frequency in four experiments ranging between 0.0003 and 0.0018. Treatment of mice with polyclonal activators known to increase the IL 4-producing capacity of T cells when assayed in bulk culture caused striking increases in the frequency of IL4-producing cells. Similarly, culturing cells in vitro with anti-CD3, IL2 and IL4 for 5 days caused a marked increase in the frequency of cells capable of producing IL4, to 0.031.IL4 production by individual T cells is dependent upon IL2. Thus, in naive T cell populations, the frequency of IL4-producing cells in response to stimulation with anti-CD3 in the absence of IL2 was below the limit of detection. T cells from primed donors showed a striking inhibition in the frequency of IL4-producing cells in response to anti-CD3 when IL2 was not present. The availability of a simple assay to measure the frequency of cells capable of producing IL4 should have substantial utility in allowing the evaluation of conditions that regulate IL4 production in vivo and in vitro.

摘要

已开发出一种能够检测单个细胞白细胞介素4(IL4)产生的有限稀释分析方法。该分析基于在IL2(5 U/ml)存在的情况下,用结合在特拉萨基孔表面的抗CD3抗体刺激T细胞。24 - 36小时后加入IL4选择性指示细胞系CT.4S的细胞,并根据此后24 - 48小时它们的存活情况测定IL4的产生。D10.G4细胞系的T细胞产生IL4的频率为0.98。来自未接触过抗原的供体且能够响应抗CD3加IL2产生IL4的T细胞非常罕见,在四个实验中的频率介于0.0003和0.0018之间。用已知在批量培养中可增加T细胞产生IL4能力的多克隆激活剂处理小鼠,导致产生IL4细胞的频率显著增加。同样,在体外将细胞与抗CD3、IL2和IL4一起培养5天,能够产生IL4的细胞频率显著增加至0.031。单个T细胞产生IL4依赖于IL2。因此,在未接触过抗原的T细胞群体中,在无IL2的情况下用抗CD3刺激时产生IL4的细胞频率低于检测限。当不存在IL2时,来自已接触过抗原的供体的T细胞在响应抗CD3时产生IL4的细胞频率表现出显著抑制。一种用于测量能够产生IL4的细胞频率的简单分析方法的可用性,在评估体内和体外调节IL4产生的条件方面应具有很大的实用价值。

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