Revisiting the identification and cDNA cloning of T cell-replacing factor/interleukin-5.

Front Immunol

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.

Published: January 2015

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.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4274987PMC
http://dx.doi.org/10.3389/fimmu.2014.00639DOI Listing

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