The Journal of Experimental Medicine · 1996 · 123 citations · 34 references
Life SciencesCell BiologyImmunologyAutoimmunityCellular ImmunologyImmunoregulationCell-mediated ImmunityImmunological MemoryT Cell ActivationT Cell BiologyT Cell ToleranceThymic DevelopmentMemory T Cell SubsetsT Cell Repertoire FormationT Cell Repertoire SelectionT-cell Receptor Repertoire DevelopmentThymic Tolerance
Rats of the PVG.RT1u strain develop autoimmune diabetes when thymectomized at 6 wk of age and are rendered relatively lymphopenic by a cumulative dose of 1,000 rads 137Cs gamma-irradiation given in four split doses. Previous studies have shown that the disease is prevented by the intravenous injection of 5 x 10(6) CD4+ CD45RC-TCR alpha beta+ RT6+ peripheral T cells from normal syngeneic donors. These cells have a memory phenotype and are presumably primed to some extrathymic antigen. However, we now report that the CD4+ CD8- population of mature thymocytes is a very potent source of cells, with the capacity to prevent diabetes in our lymphopenic animals. As few as 6 x 10(5) of these cells protect approximately 50% of recipients and the level of protection increases with cell dose. It appears that one characteristic of the intrathymic selection of the T cell repertoire is the generation of cells that regulate the autoimmune potential of peripheral T cells that have been neither clonally deleted intrathymically nor rendered irreversibly anergic in the periphery.
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T cell tolerance by clonal elimination in the thymus
John W. Kappler, Neal W. Roehm, Philippa Marrack · Cell · 1987 · 2.2K citations