Skip to main content
Log in

Inverse relationship between anti-SV40 TASA and anti-H-2 cytotoxic responses

  • Original Papers
  • Published:
Journal of Cancer Research and Clinical Oncology Aims and scope Submit manuscript

Summary

The in vitro cytotoxic response against H-2 d and H-2 b SV40-transformed fibroblasts was studied in a 40-h 3H-proline assay. A very low response against SV40 TASA is associated with the H-2d antigens on target cells: however, SV40-transformed H-2d cells are as immunogenic as SV40-transformed H-2b cells and prime against H-2b target cells. The data concerning in vitro amplification of the anti-SV40 TASA response and the involvement of cyclophosphamide-sensitive suppressor populations confirm the comparable immunogenicity of SV40-transformed H-2d and H-2b cells and cannot account for the haplotype-related behavior observed with SV40-transformed target cells. The study of the response against allogeneic SV40-transformed cells shows the reverse situation: the lower cytotoxic response is now associated with the H-2b antigens on SV40-transformed cells. As suggested by the data presented here, an interaction between SV40 TASA and H-2 antigens might be postulated.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

B6:

C57BL/6 mice

B6D2F1 :

(C57BL/6xDBA/2)F hybrid mice

CB6F1 :

(BALB/cxC57BL/6)F1 hybrid mice; E

T:

effector-to-target-cell ratio

FCS:

fetal calf serum

PBS:

phosphate-buffered saline

TASA:

tumor-associated specific antigens

References

  • Chen TR (1977) In situ detection of mycoplasma contamination in cell cultures by fluorescent Hoechst 33258 stain. Exp Cell Res 104:255–262

    Google Scholar 

  • Fujiwara H, Shearer GM (1981) Genetic control of cell-mediated lympholysis to trinitrophenyl (TNP)-modified murine syngeneic cells. I. Expression of Ir gene function at the cytotoxic precursor and helper cell levels in the response to TNP-H-2b self. J Immunol 126:1047–1051

    Google Scholar 

  • Gilheany P, Arora IK, Levy RB, Shearer GM (1981) H-2-linked genetic control of murine cell-mediated lympholysis to autologous cells modified with high and low concentrations of fluorescein isothiocyanate. Cell Immunol 59:97–105

    Google Scholar 

  • Glaser M (1979) Regulation of specific cell-mediated cytotoxic response against SV40-induced tumor associated antigens by depletion of suppressor T cells with cyclophosphamide in mice. J Exp Med 149:774–779

    Google Scholar 

  • Glaser M, Lotan R (1979) Augmentation of specific tumor immunity against a syngeneic SV40-induced sarcoma in mice by retinoic acid. Cell Immunol 45:175–181

    Google Scholar 

  • Gooding L (1979) Specificities of killing by T lymphocytes generated against syngeneic SV40-tranformants: studies employing recombinants within the H-2 complex. J Immunol 122:1002–1008

    Google Scholar 

  • Gooding L (1980) Anomalous behaviour of H-2Kb in immunity to syngeneic SV40-transformed cells: evidence for cytotoxic T cell recognition of H-2/SV40 membrane antigen complexes. J Immunol 124:1612–1619

    Google Scholar 

  • Henin Y, Gomard E, Gisselbrecht S, Levy JP (1979) Significance of the proline assay in the study of anti-MSV cell-mediated immune reactions. Br J Cancer 39:51–63

    Google Scholar 

  • Knowles BB, Koncar M, Pfizenmaier K, Solter D, Aden DP, Trinchieri G (1979) Genetic control of cytotoxic T cell response to SV40 tumor-associated specific antigen. J Immunol 122:1798–1806

    Google Scholar 

  • Maki T, Howe ML (1976) Primary in vitro sensitization of murine lymphocytes against isogeneic and allogeneic cells transformed by Simian Virus 40. J Immunol 117:1398–1401

    Google Scholar 

  • Nanni P, De Giovanni C, Galli MC, Grilli S, Lollini PL, Nicoletti G, Prodi G (1981) Minor histocompatibility antigens do not enhance BALB/c anti-SV40 TASA response. Br J Cancer 44:588–591

    Google Scholar 

  • Pfizenmaier K, Pan SH, Knowles BB (1980) Preferential H-2 association in cytotoxic T cell responses to SV40-associated specific antigens. J Immunol 124:1888–1891

    Google Scholar 

  • Röllinghoff M, Starzinski-Powitz A, Pfizenmaier K, Wagner H (1977) Cyclophosphamide-sensitive T lymphocyte suppress the in vivo generation of antigen specific cytotoxic T lymphocytes. J Exp Med 145:455–459

    Google Scholar 

  • Simpson E, Matsunaga T, Brenan M, Brunner C, Benjamin D, Hetherington C, Hurme M, Chandler P (1980) H-Y antigen as a model for tumor antigens: the role of H-2 associative antigens in controlling anti-H-Y immune responses. Transpl Proc 12:103–106

    Google Scholar 

  • Stutman O (1977) Role of H-2 histocompatibility in generation of cell-mediated cytotoxicity against virus-induced mammary tumors in C3H mice. Transpl Proc 9:1153–1155

    Google Scholar 

  • Stutman O, Shen FW, Boyse EA (1977) Ly phenotype of T cells cytotoxic for syngeneic mouse mammary tumors: evidence for T cell interactions. Proc Natl Acad Sci USA 74:5667–5671

    Google Scholar 

  • Trinchieri G, Aden DP, Knowles BB (1976) Cell-mediated cytotoxicity to SV40-specific tumor-associated antigens. Nature 261:312–314

    Google Scholar 

  • Warnatz H, Krapf F (1976) Studies on the specificity of in vitro induced lymphocytotoxicity to SV40-transformed fibroblasts. J Immunol 117:981–985

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

This work was supported by grant no. 81.01423.96 of Progetto Finalizzato “Controllo della Crescita Neoplastica” from C.N.R., Italy. C.D.G. and G.N. are in receipt of a training grant from C.N.R., Italy; P.-L.L. is in receipt of a fellowship from Fondazione Anna Villa Rusconi, Varese, Italy

Rights and permissions

Reprints and permissions

About this article

Cite this article

De Giovanni, C., Grilli, S., Lollini, PL. et al. Inverse relationship between anti-SV40 TASA and anti-H-2 cytotoxic responses. J Cancer Res Clin Oncol 106, 117–122 (1983). https://doi.org/10.1007/BF00395389

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00395389

Key words

Navigation