Skip to main content
Infection and Immunity logoLink to Infection and Immunity
. 1983 Sep;41(3):1389–1390. doi: 10.1128/iai.41.3.1389-1390.1983

Age-related loss of Lyt-1,2 cells in C58 mice results in susceptibility to lactic dehydrogenase virus-induced polioencephalomyelitis.

D M Bentley, S R Watson, R E Morris
PMCID: PMC264655  PMID: 6604028

Abstract

C58 mice (aged greater than or equal to 5 months) are susceptible to age-dependent polioencephalomyelitis, a paralytic central nervous system disease induced by lactic dehydrogenase virus. Susceptibility results from the loss of protective T cells. Data are presented showing a positive correlation between the age-related loss of Lyt-1,2 cells and the development of susceptibility to neuroparalytic lactic dehydrogenase virus infection.

Full text

PDF

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Benacerraf B., Germain R. N. A single major pathway of T-lymphocyte interactions in antigen-specific immune suppression. Scand J Immunol. 1981;13(1):1–10. doi: 10.1111/j.1365-3083.1981.tb00104.x. [DOI] [PubMed] [Google Scholar]
  2. Bentley D. M., Guckian V. A., Stinnett J. D., Morris R. E. Failure to demonstrate a role for line Ib tumor-associated surface antigen in the etiology of age-dependent polioencephalomyelitis. Mol Immunol. 1982 Aug;19(8):983–989. doi: 10.1016/0161-5890(82)90306-6. [DOI] [PubMed] [Google Scholar]
  3. Bentley D. M., Morris R. E. T cell subsets required for protection against age-dependent polioencephalomyelitis of C58 mice. J Immunol. 1982 Feb;128(2):530–534. [PubMed] [Google Scholar]
  4. Duffey P. S., Lukasewycz O. A., Martinez D., Murphy W. H. Pathogenetic mechanisms in immune polioencephalomyelitis: quantitative evaluation of protective and pathogenic effects of lymphoid cells. J Immunol. 1976 May;116(5):1332–1336. [PubMed] [Google Scholar]
  5. Duffey P. S., Martinez D., Abrams G. D., Murphy W. H. Pathogenetic mechanisms in immune polioencephalomyelitis: induction of disease in immunosuppressed mice. J Immunol. 1976 Feb;116(2):475–481. [PubMed] [Google Scholar]
  6. Germain R. N., Benacerraf B. Helper and suppressor T cell factors. Springer Semin Immunopathol. 1980 May;3(1):93–127. doi: 10.1007/BF00199927. [DOI] [PubMed] [Google Scholar]
  7. Lawton J. W., Murphy W. H. Histopathology in immune polioencephalomyelitis in C58 mice. Arch Neurol. 1973 Jun;28(6):367–370. doi: 10.1001/archneur.1973.00490240027002. [DOI] [PubMed] [Google Scholar]
  8. Martinez D., Brinton M. A., Tachovsky T. G., Phelps A. H. Identification of lactate dehydrogenase-elevating virus as the etiological agent of genetically restricted, age-dependent polioencephalomyelitis of mice. Infect Immun. 1980 Mar;27(3):979–987. doi: 10.1128/iai.27.3.979-987.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Murphy W. H., Tam M. R., Lanzi R. L., Abell M. R., Kauffman C. Age dependence of immunologically induced central nervous system disease in C58 mice. Cancer Res. 1970 Jun;30(6):1612–1622. [PubMed] [Google Scholar]
  10. Pease L. R., Murphy W. H. Co-infection by lactic dehydrogenase virus and C-type retrovirus elicits neurological disease. Nature. 1980 Jul 24;286(5771):398–400. doi: 10.1038/286398a0. [DOI] [PubMed] [Google Scholar]

Articles from Infection and Immunity are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES