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The Journal of Immunology, Vol 142, Issue 8 2695-2701, Copyright © 1989 by American Association of Immunologists
ARTICLES |
B Tartakovsky, O Axelrod, T Blankenstein and E Mozes
Department of Chemical Immunology, Weizmann Institute of Science, Rehovot, Israel.
We have recently reported that various murine T cell clones produce IL- 1. Based on this observation we have analyzed in the present study the correlation between the biological functions and the generation of different lymphokines in (T,G)-A--L specific CD4+ clones. One subset of clones--the "helper clones"--were found to provide help to primed B cells, in vitro. These cells could be shown to produce IL-1, IL-2, and B cell stimulatory factor 1 (IL-4) activities and to express mRNA encoding for these three cytokines. The second subset of clones, termed "proliferative clones", were unable to help B cells in vitro but expressed vigorous Ag-dependent proliferations. These cells did not express IL-1, IL-2, or IL-4 activities. They produced another lymphokine(s) which may be granulocyte-macrophage-CSF, or some other factor recognized by the HT2 cell line. This study further substantiates the link between T cell activities and lymphokine repertoire with a special emphasis on the potential role(s) of T cell- derived IL-1.
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