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The Journal of Immunology, 1970, 104: 798-804.
Copyright © 1970 by The American Association of Immunologists, Inc.

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Serologic Demonstration of a Thymus-Dependent Population of Lymph-Node Cells1

Michael Schlesinger2 and Ilana Yron

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

Abstract

The aim of the present study was to determine whether the sensitivity of murine lymph-node cells to isoantibodies against the {vartheta} and Ly-antigens depends on the presence of the thymus. Neonatal and adult mice of various strains were thymectomized and their lymph-node cells tested at various intervals after thymectomy. Following either neonatal or adult thymectomy, the lymph-node cells of RIII/Jem mice lost their sensitivity to the cytotoxic effect of {vartheta}-AKR antibodies. The lymph-node cells of neonatally thymectomized C57BL/6 mice became refractory to the cytotoxic effect of {vartheta}-C3H antibodies, whereas the cells of neonatally thymectomized DBA/1 mice became refractory to {vartheta}-C3H and Ly-antibodies. In C3H/An mice, neonatal thymectomy resulted in an almost complete loss of the sensitivity of lymph-node cells to {vartheta}-C3H and Ly-antibodies. Some neonatally thymectomized RIII mice were grafted with allogeneic thymuses, and their lymph nodes were examined 2 to 3 weeks later. The lymph nodes of such reconstituted animals contained cells displaying the {vartheta} isoantigenicity distinctive for the thymic graft. In addition, these lymph nodes contained a slightly greater number of host cells sensitive to {vartheta} antibodies than did the lymph nodes of thymectomized littermates which did not receive thymus grafts.

These results indicate that the lymph-node cells which are sensitive to the cytotoxic effect of {vartheta} and Ly-isoantibodies are thymus-dependent, and that at least some of them are thymus-derived. Moreover, the thymus may possibly affect the expression of the {vartheta} and Ly-antigens in lymph-node cells by an indirect control mechanism.

Footnotes

This investigation was supported by United States Public Health Service Research Agreement 6X-5148.

2 Present address: Division of Immunology, Duke University Medical Center, Durham, North Carolina 27706.







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