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通过有限稀释分析对产生白细胞介素-2的同种异体反应性人T细胞进行定量评估。

Quantitative assessment of interleukin-2-producing alloreactive human T cells by limiting dilution analysis.

作者信息

Jooss J, Zanker B, Wagner H, Kabelitz D

机构信息

Department of Medical Microbiology and Immunology, University of Ulm, F.R.G.

出版信息

J Immunol Methods. 1988 Aug 9;112(1):85-90. doi: 10.1016/0022-1759(88)90037-3.

Abstract

A limiting dilution (LD) culture system was developed to estimate the frequency of IL-2 producing alloantigen-reactive human helper T lymphocytes (HTL). E rosette-purified T cells or cell sorter-separated CD4+ and CD8+ subsets were co-cultured under LD conditions with irradiated allogeneic Epstein-Barr virus-transformed lymphoblastoid cell lines (LCL) in the absence of additional growth factors. IL-2 in microculture supernatants was detected in a bioassay combined with rapid colorimetric visualization (cleavage of MTT). Under these conditions, one out of 250-800 E+, 180-280 CD4+, and 440-1000 CD8+ T cells produced IL-2 after a culture period of 3 days. This quantitative analysis of alloantigen-specific human HTL is complete within 4 days and thus provides a rapid method with potential applications in various clinical situations, e.g., transplantation medicine.

摘要

开发了一种极限稀释(LD)培养系统,以估计产生白细胞介素-2(IL-2)的同种异体抗原反应性人类辅助性T淋巴细胞(HTL)的频率。用E花环纯化的T细胞或细胞分选仪分离的CD4+和CD8+亚群,在无额外生长因子的情况下,于LD条件下与经辐照的同种异体爱泼斯坦-巴尔病毒转化的淋巴母细胞系(LCL)共培养。微量培养上清液中的IL-2通过结合快速比色可视化(MTT裂解)的生物测定法进行检测。在这些条件下,250 - 800个E+、180 - 280个CD4+和440 - 1000个CD8+ T细胞中,有一个在培养3天后产生IL-2。这种对同种异体抗原特异性人类HTL的定量分析在4天内完成,因此提供了一种快速方法,在各种临床情况(如移植医学)中具有潜在应用价值。

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