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Nature 369:403–7 Lorenz RG, Allen PM. 1988. Direct evidence for functional self protein/Iamolecule complexes in vivo. Proc. Natl. Acad. Sci. USA 5:5220–23 Sprent J. 1994. T and B memory cells. Cell 76:315–22 Lau LL, Jamieson BD, Somasundaram T, Ahmed R. 1994. Cytotoxic T-cell memory without antigen. Nature 369:648–52 Hou S, Hyland L, Ryan KW, Portner A, Doherty PC. 1994. Virus-specific CD8+ T-cell memory determined by clonal burst size. Nature 369:652–54 Evavold BD, Sloan-Lancaster J, Wilson KJ, Rothbard JB, Allen PM.

Proc. Natl. Acad. Sci. USA 1:4057– 61 Hsu BL, Evavold BD, Allen PM. 1995. Modulation of T cell development by an endogenous altered peptide ligand. J. Exp. Med. 181:805–10 Jameson SC, Hogquist KA, Bevan MJ. 1994. Specificity and flexibility in thymic selection. Nature 369:750–52 Kawai K, Ohashi PS. 1995. Immunological function of a defined T-cell population tolerized to low-affinity self antigens. Nature 374:68–69 Windhagen A, Scholz C, H¨ollsberg P, Fukaura H, Sette A, Hafler DA. 1995. Modulation of cytokine patterns of human autoreactive T cell clones by a single amino acid substitution of their peptide February 20, 1996 9:20 Annual Reviews SLOANCHPT AR11-01 Annu.

Further development after β-chain rearrangement is marked by loss of CD25 (population E of Figure 1), then upregulation of CD4 and CD8 and rearrangement of the TCRα chain (reviewed in 43, 44). Control of exit from the CD25+ stage is probably mediated by an association of the TCR-β chain with the newly discovered pTα chain and the CD3 complex (45). Other, numerically minor, T cell lineages developing in the thymus appear to branch off at about the point of CD25 expression (43) (Figure 1). One is the Figure 1 Populations of early T precursors in the mouse thymus.

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