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The Journal of Immunology, Vol 142, Issue 2 365-373, Copyright © 1989 by American Association of Immunologists
ARTICLES |
Y Asano and T Tada
Department of Immunology, Faculty of Medicine, University of Tokyo, Japan.
The present studies were carried out to characterize the influence of the T cell maturation environment on a repertoire of Th cells, T augmenting cells, and Ts cells, which were shown to construct a minimal regulatory circuit to regulate a helper function of class II-restricted Th cells. A repertoire of keyhole limpet hemocyanin-specific Th cells was influenced predominantly by I-A molecules of the T cell maturation environment, whereas a repertoire of T augmenting cells was determined by both I-A and I-E molecules. These repertoires were not influenced by the priming with Ag. A repertoire of Ts cell factor-producing Ts cells was not influenced by the T cell maturation environment, but rather was determined by the I-J haplotype of the APC utilized for priming with Ag. In contrast, a repertoire of novel cognate type Ts cells, which inhibit class II-restricted Th cell function in a restriction- restricted manner, was influenced by both I-A and I-E molecules of the T cell maturation environment. These results demonstrate the two distinct mechanisms for generating a T cell repertoire: a selection by class II molecules of the T cell maturation environment before the priming with foreign Ag and a selection by priming with APC and Ag.
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