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69. 70. 71. mational change in T-cell receptors: role in activation and in repertoire selection. Cold Spring Harbor Symp. Quant. Biol. 54:657–66 Matsui K, Boniface JJ, Steffner P, Reay PA, Davis MM. 1994. Kinetics of Tcell receptor binding to peptide/I-Ek complexes: correlation of the dissociation rate with T-cell responsiveness. Proc. Natl. Acad. Sci. USA 91:12862–66 Valitutti S, M¨uller S, Cella M, Padovan E, Lanzavecchia A. 1995. Serial triggering of many T-cell receptors by a few peptideMHC complexes.

Another difference between embryonic and adult lymphoid development is the presence of the enzyme terminal deoxynucleotide transferase (TdT) in early T and B lineage cells of the adult but not of the embryo. This enzyme is responsible for template-independent (N region) nucleotide addition during antigenreceptor gene rearrangement; this introduces an additional level of diversity into both the TCR and immunoglobulin (Ig) repertoire (9–11). Lymphoid cells produced during adult life have this additional N region diversity, while lymphoid cells produced during embryonic life do not; however, adult mice lacking TdT because of a mutated gene have an “immature lymphocyte repertoire” with few N nucleotides (10, 11).

J. Exp. Med. 181:375–80 Bu J-Y, Shaw AS, Chan AC. 1995. Analysis of the interaction of ZAP-70 and syk protein-tyrosine kinases with the T-cell antigen receptor by plasmon resonance. Proc. Natl. Acad. Sci. USA 92:5106–10 Irving BA, Chan AC, Weiss A. 1993. Functional characterization of a signal transducing motif present in the T cell antigen receptor ζ -chain. J. Exp. Med. 177:1093–103 Letourneur F, Klausner RD. 1992. Activation of T cells by a tyrosine kinase activation domain in the cytoplasmic tail of CD3- .

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Annual Review of Immunology Volume 14 1996 by Annual Reviews

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