Takatsu Kiyoshi
Toyama Prefectural Institute for Pharmaceutical Research , Imizu City, Toyama , Japan ; Department of Immunobiology and Pharmacological Genetics, Graduate School of Medicine and Pharmaceutical Sciences , Toyama City, Toyama , Japan.
Front Immunol. 2014 Dec 23;5:639. doi: 10.3389/fimmu.2014.00639. eCollection 2014.
This is a perspective based on the paper "Cloning of complementary DNA encoding T cell-replacing factor and identity with B cell growth factor II," by Kinashi et al. (1). We have been interested in understanding the molecular basis of T-B cell cooperation for antibody formation. Although many investigators had described a number of different soluble factors that appeared to have biological relevance to T-B cell interactions, molecular basis of such active substances remained unknown for a long period of time. In this perspective, I will briefly summarize the history of the initial discovery of T cell-replacing factor/B cell growth factor II that appeared to be involved in B cell growth and differentiation, and outline the discovery and characterization of interleukin-5. Studies of interleukin-5 have provided strong evidence that a single cytokine exerts a variety of activities on diverse target cells.
这是基于Kinashi等人(1)发表的论文《编码T细胞替代因子的互补DNA的克隆及其与B细胞生长因子II的同一性》的一篇综述。我们一直致力于了解T细胞与B细胞协作形成抗体的分子基础。尽管许多研究者描述了一些似乎与T细胞和B细胞相互作用具有生物学相关性的不同可溶性因子,但这些活性物质的分子基础在很长一段时间内仍不为人知。在这篇综述中,我将简要总结最初发现的似乎参与B细胞生长和分化的T细胞替代因子/B细胞生长因子II的历史,并概述白细胞介素-5的发现和特性。对白细胞介素-5的研究提供了强有力的证据,证明单一细胞因子可对多种靶细胞发挥多种作用。