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The Journal of Immunology, 1975, 115: 827-833.
Copyright © 1975 by The American Association of Immunologists, Inc.

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Subpopulations of Human Thymus Cells Differing in Their Capacity to form Stable E-Rosettes and in Their Immunologic Reactivity1

Uri Galili and Michael Schlesinger

From the Department of Experimental Medicine and Cancer Research, The Hebrew University-Hadassah Medical School, Jerusalem, Israel

Abstract

The majority of human thymus cells from young donors form stable E-rosettes with sheep red blood cells (SRBC) that do not disintegrate after prolonged incubation at 37°C. With advancing age the proportion of thymus cells forming such rosettes decreases gradually. The thymus of a patient receiving prednisone treatment was found to contain only a few cells that formed stable E-rosettes.

The minor population of thymus cells that fails to form stable E-rosettes (non-rosetting or NR cells) was isolated and tested for its cell surface markers and immunologic reactivity in vitro. Most of the NR-cells were capable of forming regular E-rosettes with SRBC at room temperature. Like the majority of human thymus cells they were sensitive to the cytotoxic effect of normal rabbit serum. Lymphocytes with B cell markers constituted less than 0.2% of the original thymus cell suspensions, but about 1 to 3% of the NR-population.

Thymus cells from donors over the age of 36 and from a prednisone-treated child responded in vitro to stimulation with either phytohemagglutinin (PHA) or concanavalin A (Con A). Unfractionated thymus cells from children up to the age of 14 failed to react to either PHA or Con A, but their NR-population responded vigorously to both lectins. In contrast to unfractionated thymus cell suspensions from children, the NR fraction showed a significant reactivity in mixed lymphocyte cultures with mitomycin-C treated allogeneic lymphocytes.

It is concluded that like the thymus of other species, the human thymus contains a minor population of cortisone-resistant cells endowed with many of the immunologic properties characteristic for peripheral T lymphocytes.

Footnotes

1 This study was supported by a grant from the Goldhirsch Foundation and by a Lady Davis Endowment.







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