Abstract
In 1976, Morgan and his associates [1] first reported that interleukin-2 (IL-2) was a T-cell growth factor. Since then, various biological activities of IL-2 [2] have been elucidated, including proliferation of T cells, natural killer (NK) cells, and lymphokine-activated killer (LAK) cells; induction of cytotoxicity of killer T cells, NK cells, LAK cells, and monocytes; induction of lymphokine production such as interferon, EL-3, -4, -5, -6, colony stimulating factor, and tumor necrosis factor; and induction of receptors.
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© 1991 Springer-Verlag Berlin Heidelberg
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Aso, Y., Tazaki, H., Umeda, T., Marumo, K. (1991). Treatment of Advanced Renal Cell Carcinoma by Systemic Low-Dose Recombinant Interleukin-2. In: Debruyne, F.M.J., Bukowski, R.M., Pontes, J.E., de Mulder, P.H.M. (eds) Immunotherapy of Renal Cell Carcinoma. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-75853-9_14
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DOI: https://doi.org/10.1007/978-3-642-75853-9_14
Publisher Name: Springer, Berlin, Heidelberg
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