1887

Abstract

SUMMARY

Malignant rabbit fibroma virus (MV) is a lymphocytotropic leporipoxvirus which produces profound immunological dysfunction and lethal fibromyxosarcoma. We examined virus recovery from splenic lymphocytes as a function of time after inoculation , and correlated this with both immunological function and expression of virus-induced host suppressor activity. MV was most abundant in lymphocytes obtained 4 days following inoculation. At that time, immune function was relatively normal and host suppressor activity was not observed. By 7 days after infection, when active host immunosuppressor functions were observed, virus recovery was decreased. Eleven days post-inoculation host immune function began to recover despite increasing virus-induced tumours and developing opportunistic infection. Simultaneously, MV was no longer recoverable from spleen cells. Spleen cells from day 11 tumour-bearing rabbits did not support MV replication as efficiently as did normal or day 4 or 7 splenic lymphocytes, but they did not alter the ability of MV to grow in the latter cells. By fluorescence examination and cytofluorography, splenic lymphocytes bearing MV antigens were abundant 7 days after infection but disappeared by 11 days. This was temporally related to production of neutralizing antibody to MV, and development of virus-specific lymphocyte proliferative activity. The composition of splenic lymphocytes changed as well: the normal ratio of about 1:1 for B and T cells changed to 1:2 by day 7, and then inverted to almost 2 :1 by day 11. Rabbits infected with MV thus appear to recover their immune function, concurrently eliminate virus-infected lymphocytes, and elaborate high titres of neutralizing serum antibodies despite progressive infections and tumour development.

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1987-02-01
2024-12-09
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References

  1. Bartholomew R. M., Esser A. F., Muller-Eberhard H. J. 1978; Lysis of oncornaviruses by human serum: isolation of the viral complement (C1) receptor and identification as p15E. Journal of Experimental Medicine 147:844–853
    [Google Scholar]
  2. Biron C. A., Habu S., Okumura K., Welsh R. M. 1984; Lysis of uninfected and virus-infected cells in vivo: a rejection mechanism in addition to that mediated by natural killer cells. Journal of Virology 50:698–707
    [Google Scholar]
  3. Block W., Upton C., McFadden G. 1985; Tumorigenic poxviruses: genomic organization of malignant rabbit virus, a recombinant between Shope fibroma virus and myxoma virus. Virology 140:113–124
    [Google Scholar]
  4. Bukowski J. F., Woda B. A., Habu S., Okumura K., Welsh R. M. 1983; Natural killer cell depletion enhances virus synthesis and virus-induced hepatitis in vivo . Journal of Immunology 131:1531–1538
    [Google Scholar]
  5. Fujunami R. s., Oldstone M. B. A. 1984; Antibody initiates viral persistence: immune modulation and measles virus infection. In Concepts in Viral Pathogenesis pp. 187–193 Notkins A. L., Oldstone M. B. A. Edited by New York: Springer-Verlag;
    [Google Scholar]
  6. Habu S., Fukui H., Shimanura K., Kasai M., Nagai Y., Okumura K., Tamaoki N. 1981; In vivo effects of antiasialo GM1. Reduction of NK activity and enhancement of transplanted tumor growth in nude mice. Journal of Immunology 127:34–38
    [Google Scholar]
  7. Habu S., Shimanura K., Akamatsu K. -I., Okumura K., Tamaoki N. 1984; Protective role of natural killer cells in tumor growth and viral infection in mice. In Immune-Deficient Animals: 4th International Workshop on Immune-Deficient Animals in Experimental Research pp. 40–43 Sordat B. Edited by Basel: S. Karger;
    [Google Scholar]
  8. Heitzmann H., Richards F. M. 1974; Use of the avidin-biotin complex for specific staining of biological membranes in electron microscopy. Proceedings of the National Academy of Sciences, U.S.A 71:3537–3541
    [Google Scholar]
  9. Hicks J. T., Ennis F. A., Kim E., Verbonitz M. 1978; The importance of an intact complement pathway in recovery from a primary viral infection. Influenza in decomplemented and in C5-deficient mice. Journal of Immunology 121:1437–1445
    [Google Scholar]
  10. Hirsch R. L., Winkelstein J. A., Griffen D. E. 1980; The role of complement in viral infections. Journal of Immunology 124:2507–2510
    [Google Scholar]
  11. Holland J., Kennedy S. I. T., Semler B. L., Jones C. L., Roux L., Grabau E. A. 1980; Defective interfering particles in host resistance. In Comprehensive Virology 16 pp. 137–192 Fraenkel-Conrat H., Wagner R. R. Edited by New York: Plenum Press;
    [Google Scholar]
  12. Mcmichael A., Hildreth J. E. K. 1982; Virus specific cytotoxic T cells. In Human Immunity to Viruses pp. 3–19 Ennis F. A. Edited by New York: Academic Press;
    [Google Scholar]
  13. Mcnicholas J. M., Watkins J. R., Johnson A. D., Knight K. L. 1981; Functional studies of rabbit T lymphocytes. Immunology 43:635–641
    [Google Scholar]
  14. Mogensen S. C. 1979; Role of macrophages in natural resistance to virus infection. Micrological Reviews 43:1–26
    [Google Scholar]
  15. Nayak D. P., Chambers T. M., Akkina R. K. 1985; Defective-interfering (DI) RNAs of influenza viruses: origin, structure, expression and interference. Current Topics in Microbiology and Immunology 114:104–151
    [Google Scholar]
  16. Padgett B. L., Moore M. s., Walker D. L. 1962; Plaque assays for myxoma and fibroma viruses and differentiation of the virus by plaque formation. Virology 17:462–469
    [Google Scholar]
  17. Perlmann P. 1984; Antibody-dependent cellular toxicity (ADCC) mediated by human killer lymphocytes (K cells). In Concepts in Viral Pathogenesis pp. 55–64 Notkins A. L., Oldstone M. B. A. Edited by New York: Springer-Verlag;
    [Google Scholar]
  18. Perrault J. 1981; Origin and replication of defective interfering particles. Current Topics in Microbiology and Immunology 93:151–207
    [Google Scholar]
  19. Redelman D., Scott C. B., Sheppard H. W. JR Sell S. 1976; In vitro studies of the rabbit immune system. II. Functional characterization of rabbit T and B populations separated by adherence to nylon wool or lysis with antithymocyte serum and complement. Cellular Immunology 24:11–23
    [Google Scholar]
  20. St. Geme J. W. JR Prince J. T., Burke B. A., Good R. A., Krivit W. 1965; Impaired cellular resistance to herpes-simplex-virus in Wiscott-Aldrich syndrome. New England Journal of Medicine 273:229–234
    [Google Scholar]
  21. Sheppard H. w. JR Redelman D., Sell S. 1976; In vitro studies of the rabbit immune system. IV. Differential mitogen responses of isolated T and B cells. Cellular Immunology 24:34–44
    [Google Scholar]
  22. Sissons J. G. P., Oldstone M. B. A. 1980; Antibody-mediated destruction of virus-infected cells. Advances in Immunology 29:209–259
    [Google Scholar]
  23. Skaletsky E., Sharp P. A., Sell S., Strayer D. S. 1984; Immunologic dysfunction during viral oncogenesis. II. Inhibition of cellular immunity to viral antigens by malignant rabbit fibroma virus. Cellular Immunology 86:64–74
    [Google Scholar]
  24. Strayer D. s., Leibowitz J. L. 1986; Reversal of virus-induced immunosuppression. Journal of Immunology 136:2649–2653
    [Google Scholar]
  25. Strayer D. S., Sell S. 1983; Immunohistology of malignant rabbit fibroma virus - a comparative study with rabbit myxoma virus. Journal of the National Cancer Institute 71:105–116
    [Google Scholar]
  26. Strayer D. S., Skaletsky E., Cabirac G., Sharp P. A., Corbeil L. B., Sell S., Leibowitz J. L. 1983a; Malignant rabbit fibroma virus causes secondary immunosuppression in rabbits. Journal of Immunology 130:399–404
    [Google Scholar]
  27. Strayer D. S., Cabirac G. F., Sell S., Leibowitz J. L. 1983b; Malignant rabbit fibroma virus: observations on the cultural and histopathologic characteristics of a new virally-induced tumor syndrome. Journal of the National Cancer Institute 71:91–104
    [Google Scholar]
  28. Strayer D. S., Sell S., Skaletsky E., Leibowitz J. L. 1983c; Immunologic dysfunction during viral oncogenesis. I. Nonspecific immunosuppression caused by malignant rabbit fibroma virus. Journal of Immunology 131:2595–2600
    [Google Scholar]
  29. Strayer D. S., Skaletsky E., Leibowitz J. L. 1985a; In vitro growth of two related leporipoxviruses in lymphoid cells. Virology 145:330–334
    [Google Scholar]
  30. Strayer D. S., Sell S., Leibowitz J. L. 1985b; Animal model of human disease: malignant rabbit fibroma syndrome: a possible model for acquired immunodeficiency syndrome AIDS. American Journal of Pathology 120:170–171
    [Google Scholar]
  31. Verna J. E., Eylar O. R. 1962; Rabbit fibroma virus plaque assay and in vitro studies. Virology 18:266–273
    [Google Scholar]
  32. Welsh R. M. JR 1977; Host modification of lymphocytic choriomeningitis virus and Newcastle disease virus altering viral inactivation by human complement. Journal of Immunology 118:348–354
    [Google Scholar]
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