Transplantable reticulum cell sarcomas (RCS) of SJL mice fail to grow in immunocompromised, syngeneic recipients and induce marked proIiferation of Lyt-1?+?, 2?-? host T cells, without the development of RCS-specific cytotoxic cells. These phenomena appear to be under strict I-region gene control. Additionally, whereas normal SJL mice are classified as a """"""""low"""""""" natural killer (NK) cell strain, lymphoid tissues from SJL mice bearing spontaneous, primary RCS or transplantable RCS lines exhibit high levels of NK activity. Previous studies have suggested that the major part of this NK activity is mediated by the tumor cells themselves. Thus, this may represent a unique mechanism by which tumor cells circumvent and/or overcome immune rejection. Given the apparent pre-B cell nature of RCS tumors (Thy-1?-?, sIg?-?, Ia?+?, Lyb-2?+?), it is critical to unequivocally demonstrate their NK-like and -associated (i.e., interferon production) functions. This will be achieved in these studies by specifically isolating cells with NK cytolytic potential from tumorous lymphoid tissue and correlating their cytotoxic function with other characteristic properties of RCS cells: (1) progressive tumor growth; (2) expression of RCS surface determinants; (3) capacity to stimulate syngeneic T cells; and (4) homing properties to B-cell areas of lymph nodes. The host component of the observed, RCS-associated NK activity will also be further characterized. Using lymphocyte growth factors and hybridization methodology, in vitro cell lines of RCS tumor cells and of the responding host T cells that they stimulate will be produced. Analysis of such cloned cell lines will be invaluable in addressing many of the questions regarding cell lineage, surface phenotype, and functional properties, as well as tanget-receptor specificity of the cellular participants in RCS-associated NK activity. Since this murine lymphoma exhibits many similarities to some B-cell malignancies in humans, these studies may reveal significant host-tumor interactions that can be of potential benefit in the diagnosis and treatment of human disease. (MI)

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA034549-03
Application #
3172279
Study Section
Immunobiology Study Section (IMB)
Project Start
1983-04-01
Project End
1986-06-30
Budget Start
1985-04-01
Budget End
1986-06-30
Support Year
3
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Medicine & Dentistry of NJ
Department
Type
Schools of Medicine
DUNS #
605799469
City
Newark
State
NJ
Country
United States
Zip Code
Lin, T Z; Fernandes, H; Yauch, R et al. (1992) IL-10 production in a CD5+ B cell lymphoma arising in a CD4 monoclonal antibody-treated SJL mouse. Clin Immunol Immunopathol 65:10-22
Lin, T Z; Ponzio, N M (1991) Syngeneic B lymphoma cells provide a unique stimulus to natural killer (NK) cells in genetically low-NK SJL/J mice. J Leukoc Biol 49:48-57
Alisauskas, R M; Friedman, C A; Ponzio, N M (1990) Influence of T-helper cell specific monoclonal antibody on progressive growth of B-cell lymphomas in SJL/J mice: correlation of acute treatment dosage with tumor dormancy or complete remission in long-term survivors. Cancer Commun 2:33-43
Alisauskas, R M; Ponzio, N M (1989) T-helper-cell-specific monoclonal antibody inhibits growth of B-cell lymphomas in syngeneic SJL/J mice. Cell Immunol 119:286-303
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Lasky, J L; Ponzio, N M; Thorbecke, G J (1988) Characterization and growth factor requirements of SJL lymphomas. I. Development of a B cell growth factor-dependent in vitro cell line, cRCS-X. J Immunol 140:679-87
Ponzio, N M; Alonso, A; Alisauskas, R M (1987) Dependence of lymphoma growth on 'reversed immunological surveillance'. Pathol Immunopathol Res 6:1-21
Ponzio, N M; Brown, P H; Thorbecke, G J (1986) Host-tumor interactions in the SJL lymphoma model. Int Rev Immunol 1:273-301
Alisauskas, R M; Ponzio, N M (1986) In vivo growth inhibition of Ia+ lymphomas in SJL mice treated with I-As-reactive monoclonal antibody. Immunopharmacology 12:1-9
DeKruyff, R H; Brown, P H; Thorbecke, G J et al. (1985) Characterization of SJL T cell clones responsive to syngeneic lymphoma (RCS): RCS-specific clones are stimulated by activated B cells. J Immunol 135:3581-6

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