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. 1975 Dec;12(6):1464–1469. doi: 10.1128/iai.12.6.1464-1469.1975

Effect of neonatal thymectomy on experimental subacute sclerosing panencephalitis in adult hamsters.

K P Johnson, E G Feldman, D P Byington
PMCID: PMC415456  PMID: 1205623

Abstract

Syrian golden hamsters were thymectomized in the first 48 h of life, raised, and then inoculated intracerebrally with the HBS strain of hamster-adapted subacute sclerosing panencephalitis virus when over 12 weeks old. Two groups soon become apparent; one group showed progressive neurological susmptoms and the other group remained healthy. The sick hamsters became moribund between days 8 and 17 postinoculation, and they had large amounts of complete virus in their brains, no antibodies to measles virus in their sera, and a demonstrated lack of thymus tissue. Pathological changes in the central nervous system included marked focal necrosis, numerous giant and inclusion-bearing cells, and slight inflammation. The healthy animals, killed at day 22 or 35 postinoculation, contained no central nervous system virus, moderate amounts of measles antibody in their sera, minimal or absent central nervous system pathology, and histologically identifiable remnants of thymus tissue. These studeis indicate that, in the hamster, the immune system is essential in recovering from central nervous system measles infection and that the antibody response to measles probably requires helper T lymphocytes to develop. Im the absence of antibody to measles, the virus did not undergo modification to a cell-associated state, as noted in previous hamster studies and in human subacute aclerosing panencephalitis. This model system may be useful for passive transfer studies to further clarify the effect of the n vivo immune response to acute and persistent central nervous system measles virus infections9

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Selected References

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  1. Ahmed A., Strong D. M., Sell K. W., Thurman G. B., Knudsen R. C., Wistar R., Jr, Grace W. R. Demonstration of a blocking factor in the plasma and spinal fluid of patients with subacute sclerosing panencephalitis. I. Partial characterization. J Exp Med. 1974 Apr 1;139(4):902–924. doi: 10.1084/jem.139.4.902. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Akhtar M., Young I. Measles giant cell pneumonia in an adult following long-term chemotherapy. Arch Pathol. 1973 Sep;96(3):145–148. [PubMed] [Google Scholar]
  3. Breitfeld V., Hashida Y., Sherman F. E., Odagiri K., Yunis E. J. Fatal measles infection in children with leukemia. Lab Invest. 1973 Mar;28(3):279–291. [PubMed] [Google Scholar]
  4. Byington D. P., Castro A. E., Burnstein T. Adaptation to hamsters of neurotropic measles virus from subacute sclerosing panencephalitis. Nature. 1970 Feb 7;225(5232):554–555. doi: 10.1038/225554b0. [DOI] [PubMed] [Google Scholar]
  5. Byington D. P., Johnson K. P. Experimental subacute sclerosing panencephalitis in the hamster: correlation of age with chronic inclusion-cell encephalitis. J Infect Dis. 1972 Jul;126(1):18–26. doi: 10.1093/infdis/126.1.18. [DOI] [PubMed] [Google Scholar]
  6. Byington D. P., Johnson K. P. Subacute sclerosing panencephalitis (SSPE) agent in hamsters. II. The neuropathology of acute and chronic infections. Exp Mol Pathol. 1973 Jun;18(3):345–356. doi: 10.1016/0014-4800(73)90030-0. [DOI] [PubMed] [Google Scholar]
  7. Byington D. P., Johnson K. P. Subacute sclerosing panencephalitis virus in immunosuppressed adult hamster. Lab Invest. 1975 Jan;32(1):91–97. [PubMed] [Google Scholar]
  8. Connolly J. H. Subacute sclerosing panencephalitis. Postgrad Med J. 1972 Jun;48(560):342–345. doi: 10.1136/pgmj.48.560.342. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. GOOD R. A., ZAK S. J. Disturbances in gamma globulin synthesis as experiments of nature. Pediatrics. 1956 Jul;18(1):109–149. [PubMed] [Google Scholar]
  10. Horta-Barbosa L., Hamilton R., Wittig B., Fuccillo D. A., Sever J. L., Vernon M. L. Subacute sclerosing panencephalitis: isolation of suppressed measles virus from lymph node biopsies. Science. 1971 Aug 27;173(3999):840–841. doi: 10.1126/science.173.3999.840. [DOI] [PubMed] [Google Scholar]
  11. Johnson K. P., Byington D. P., Gaddis L. Subacute sclerosing panencephalitis. Adv Neurol. 1974;6:77–86. [PubMed] [Google Scholar]
  12. Johnson K. P., Norrby E. Subacute sclerosing panencephalitis (SSPE) agent in hamsters. 3. Induction of defective measles infection in hamster brain. Exp Mol Pathol. 1974 Oct;21(2):166–178. doi: 10.1016/0014-4800(74)90087-2. [DOI] [PubMed] [Google Scholar]
  13. Kibler R., Cremer N. E. Antithymocyte serum treatment of hamsters inoculated with a measles virus isolated from a patient with subacute sclerosing panencephalitis. Immunol Commun. 1973;2(3):303–321. doi: 10.3109/08820137309022802. [DOI] [PubMed] [Google Scholar]
  14. McFarland H. F. The effect of measles virus infection on T and B lymphocytes in the mouse. I. Suppression of helper cell activity. J Immunol. 1974 Dec;113(6):1978–1983. [PubMed] [Google Scholar]
  15. Notkins A. L. Immune mechanisms by which the spread of viral infections is stopped. Cell Immunol. 1974 Mar 30;11(1-3):478–483. doi: 10.1016/0008-8749(74)90045-8. [DOI] [PubMed] [Google Scholar]
  16. ROOSA R. A., WILSON D. B., DEFENDI V. EFFECT OF THYMECTOMY ON HAMSTERS. Proc Soc Exp Biol Med. 1965 Mar;118:584–590. doi: 10.3181/00379727-118-29911. [DOI] [PubMed] [Google Scholar]
  17. Raine C. S., Byington D. P., Johnson K. P. Experimental subacute sclerosing panencephalitis in the hamster. Ultrastructure of the chronic disease. Lab Invest. 1974 Oct;31(4):355–368. [PubMed] [Google Scholar]
  18. Raine C. S., Byington D. P., Johnson K. P. Subacute sclerosing panencephalitis in the hamster. Ultrastructure of the acute disease in newborns and weanlings. Lab Invest. 1975 Aug;33(2):108–116. [PubMed] [Google Scholar]
  19. STARR S., BERKOVICH S. EFFECTS OF MEASLES, GAMMA-GLOBULIN-MODIFIED MEASLES AND VACCINE MEASLES ON THE TUBERCULIN TEST. N Engl J Med. 1964 Feb 20;270:386–391. doi: 10.1056/NEJM196402202700802. [DOI] [PubMed] [Google Scholar]
  20. Stevens J. G., Cook M. L. Maintenance of latent herpetic infection: an apparent role for anti-viral IgG. J Immunol. 1974 Dec;113(6):1685–1693. [PubMed] [Google Scholar]
  21. Wear D. J., Rapp F. Latent measles virus infection of the hamster central nervous system. J Immunol. 1971 Dec;107(6):1593–1598. [PubMed] [Google Scholar]

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