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Compared to the last twenty years of lymphokine research, the past two years of effort directed towards understanding the T-lymphocytotrophic hormone, interleukin 2 OL-2) (1-3), have resulted in an exponential increase in our gra.�p of the importance of intercellular communicating molecules. As in many other fields of biology, breakthroughs have resulted from the application of monoclonal antibodies and molecular biology to this area of research. In addi tion. an endocrinologic approach has provided fresh insight into the mecha nism whereby IL·2 promotes T-cell proliferation. Consequently, the tools are at last available for new experimental approaches to fundamental questions in im!llUnology and cell biology. The idea that lymphocytes are stimulated to undergo DNA duplication and mitosis by antigen triggering of specific receptors has slowly evolved to the understanding that while this concept is correct, the process is carried forward by discernible molecular mechanisms. Through painstaking cellular and bio chemical experiments a consensus has finally been reached that IL-2 is a critical biologic activity, released from antigen-triggered lymphocytes within hours of activation, that functions to mediate a switch in T cells from 01 into the proliferative phases (i.e. S, O2, and M) of the cell cycle. However, until re cent
Annual Review of Immunology – Annual Reviews
Published: Apr 1, 1984
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