Abstract
The existence of specific tumor rejection antigens was first demonstrated with chemically induced mouse sarcomas: each tumor was found to express a different antigen [1]. Similar findings were made with ultraviolet-induced tumors [2]. Later, the generality of the existence of tumor rejection antigens was questioned when spontaneous mouse tumors were found to be completely incapable of eliciting an immune rejection response [3]. However, further experiments demonstrated that even these tumors express weak transplantation antigens that are potential targets for immune rejection by the syngeneic host [4].
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Prehn RT, Main JM (1957) Immunity to methylcholanthrene-induced sarcomas. INCI 18:769
Kripke MI (1981) Immunologic mechanism in UV radiation carcinogenesis. Adv Cancer Res 34:69
Hewitt HB, Blake ER, Walder AS (1976) A critique of the evidence for active host defense against cancer based on personal studies of 27 murine tumors of spontaneous origin. Br J Cancer 33:241
Van Pel A, Vessière F, Boon T (1983) Protection against two spontaneous mouse leukemias conferred by immunogenic variants obtained by mutagenesis. J Exp Med 157:1992
Boon T, Kellerman O (1977) Rejection by syngeneic mice of cell variants obtained by mutagenesis of a malignant terato-carcinoma cell line. Proc Natl Acad Sci USA 74:272
Frost P, Kerbel R, Bauer E, Tartamella-Biondo R, Cefalu W (1983) Mutagen treatments as a means for selecting immunogenic variants from otherwise poorly immunogenic malignant murine tumors. Cancer Res 43:125
Boon T, van Pel A (1978) Teratocar-cinoma cell variants rejected by syngeneic mice: protection of mice immunized with these variants against other variants and against the original malignant cell line. Proc Natl Acad Sci USA 75:1519
Boon T, van Snick J, van Pel A, Uyttenhove C, Marchand M (1980) Immunogenic variants obtained by mutagenesis of mouse mastocytoma P815. T lymphocyte-mediated cytolysis. J Exp Med 152:1184
Maryanski JL, van Snick J, Cerottini JC, Boon T (1982) Immunogenic variants obtained by mutagenesis of mouse mastocytoma P815. Clonal analysis of the syngeneic cytolytic T lymphocyte response. Eur J Immunol 12:401
Maryanski JL, Boon T (1982) Immunogenic variants obtained by mutagenesis of mouse mastocytoma P815. Analysis of variants-specific antigens by selection of antigen-loss variants with cytolytic T-cell clones. Eur J Immunol 12:406
Maryanski J, Marchand M, Uyttenhove C, Boon T (1983) Immunogenic variants obtained by mutagenesis of mouse mastocytoma P815. Occasional escape from host rejection due to antigen-loss secondary variants. Int J Cancer 31:119
Van Pel A, de Plaen E, Boon T (1985) Selection of highly transfectable variant from mouse mastocytoma P815. Somatic Cell Mol Genet 11:467
Wölfel T, van Pel A, de Plaen E, Lurquin C, Maryanski JL, Boon T (1987) Immunoenic (tum-) variants obtained by mutagenesis of mouse mastocytoma P815. Detection of stable transfectants expressing a tun - antigen with a cytolytic T cell stimulation assay. Immunogenetics 26:178
De Plaen E, Lurquin C, van Pel A, Mariamé B, Szikora JP, Wölfel T, Sibille C, Chomez P, Boon T (1988) Immunogenic (tum−) variants of mouse tumor P815: cloning of the gene of tun− antigen P91A and identification of the tun− mutation. Proc Natl Acad Sci USA 85:2274
Szikora JP, van Pel A, Brichard V, André M, van Baren N, Henry P, de Plaen E, Boon T (1990) Structure of the gene of tun- transplantation antigen P35B: pre-sence of a point mutation in the antigenic allele. EMBO J 9:1041
Sibille C, Chomez P, Wildmann C, van Pel A, de Plaen E, Maryanski JL, de Bergeyck V, Boon T (1990) Structure of the gene of tun- transplantation antigen P198: a point mutation generates a new antigenic peptide. J Exp Med 172:35
Lurquin C, van Pel A, Mariamé B, de Plaen E, Szikora JP, Janssens C, Reddehase MJ, Lejeune J, Boon T (1989) Structure of the gene of tun- transplantation antigen P91 A: the mutated exon encodes a peptide recognized with Ld by cytolytic T cells. Cell 58:293
Townsend ARM, Gotch FM, Davey J (1985) Cytotoxic T cells recognize fragments of the influenza nucleoprotein. Cell 42:457
Townsend ARM, Rothbard J, Gotch FM, Bahadur G, Wraith D, McMichael AJ (1986) The epitopes of influenza nucleoprotein recognized by cytotoxic T lymphocytes can be defined with short synthetic peptides. Cell 44:959
Townsend ARM, Bastin J, Gould K, Brownlee GG (1986) Cytotoxic T lymphocytes recognize influenza haemagglu-tinin that lacks a signal sequence. Nature 324:575
Van den Eynde B, Lethé ?, van Pel A, de Plaen E, Boon T (1991) The gene coding for the main tumor rejection antigen of mouse tumor P815 is identical to the normal gene of the syngeneic DBA/2 mice. J Exp Med 173:1373
Uyttenhove C, Maryanski J, Boon T (1983) Escape of mouse mastocytoma P815 after nearly complete rejection is due to antigen-loss variants rather than immunosuppression. J Exp Med 157:1040
Hültner L, Moeller J, Schmitt E, Jäger G, Reisbach G, Ring J, Dörmer P (1989) Thiol-sensitive mast cell lines derived from mouse bone marrow respond to a mast cell growth-enhancing activity different from both IL-3 and IL-4. J Immunol 142:3440
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1992 Springer-Verlag Berlin Heidelberg
About this paper
Cite this paper
Van den Eynde, B., Lethé, B., Van Pel, A., Boon, T. (1992). Tumor Rejection Antigens and Immune Surveillance. In: Neth, R., Frolova, E., Gallo, R.C., Greaves, M.F., Afanasiev, B.V., Elstner, E. (eds) Modern Trends in Human Leukemia IX. Haematology and Blood Transfusion / Hämatologie und Bluttransfusion, vol 35. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-76829-3_42
Download citation
DOI: https://doi.org/10.1007/978-3-642-76829-3_42
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-540-54360-2
Online ISBN: 978-3-642-76829-3
eBook Packages: Springer Book Archive