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The Journal of Immunology, 1979, 123: 1110-1116.
Copyright © 1979 by The American Association of Immunologists, Inc.

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Lymphocytes Surface Membrane Immunoglobulin in Myeloma

I. M315-Bearing T Lymphocytes in Mice with MOPC-3151

Howard M. Gebel2, Richard G. Hoover3 and Richard G. Lynch4

Department of Pathology and Division of Biology and Biomedical Sciences, Washington University School of Medicine, St. Louis, Missouri 63110

Abstract

MOPC-315 is a BALB/c plasmacytoma that produces an IgA anti-TNP antibody (M315). 315/+ is a line derived from MOPC-315 and differentiates during in vivo growth from M315-producing, nonsecreting, lymphocytoid cells to large M315-secreting plasmacytoid cells. Studies were conducted to determine whether the small M315-bearing mononuclear cells, which account for more than one-third of the circulating mononuclear cells in mice with 315/+ tumors, were myeloma cells or host lymphocytes. Experiments conducted in CBF1 mice demonstrated that the circulating M315-bearing cells were of F1, rather than tumor, origin. Serologic and ultrastructural studies demonstrated that the cells were post-thymic T lymphocytes. After proteolytic removal, surface M315 was reexpressed in vitro by 315/+ cells, but not by T cells. M315-bearing T cells accounted for 0 to 4% of circulating mononuclear cells in mice with 315/P, a variant of MOPC-315 in which all cells synthesize M315, but only 2% of the cells are secretory. There was no obvious relationship between the frequency of M315-bearing lymphocytes and development of the humoral immunodeficiency that accompanies myeloma. These findings 1) identify an association between high levels of M315 secretion and development of M315-bearing T cells; 2) favor the view that M315 is acquired, rather than produced by host T cells; 3) raise the possibility that T cells with IgA-Fc receptors may be increased in mice with 315/+ tumors; and 4) are discussed relative to the mechanisms that have been proposed in the literature to account for the occurrence and significance of circulating, M-component-bearing lymphoid cells in murine and human myeloma.

Footnotes

1 This work was supported by United States Public Health Service research Grants CA17114 and CA23217 and by a special grant to the Department of Pathology from the following companies: Brown & Williamson Tobacco Corporation; Larus and Brother Company, Inc.; Liggett & Meyers, Incorporated; Lorillard, a Division of Loews Theatres, Incorporated; Philip Morris, Incorporated; R. J. Reynolds Tobacco Company; United States Tobacco Company; and Tobacco Associates, Inc.

2 Supported by United States Public Health Service Training Grant GM-09118.

3 Supported by Medical Scientists Training Program and Grant GM-02016.

4 Reprint requests: 660 South Euclid Avenue, St. Louis, Missouri 63110.







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