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Effect of Corynebacterium granulosum immunopotentiation on the pathogenesis of herpes simplex virus type 2 in BALB/c mice.

Abstract
Treatment of 4- to 6-week-old, 18- to 22-g male BALB/c mice with 0.6 mg of Corynebacterium granulosum resulted in a significant decrease in mortality due to challenge with herpes simplex virus type 2 (HSV-2). Optimal protection occurred when C. granulosum was injected 1 week before HSV-2 infection. C. granulosum-induced resistance to HSV-2 lasted up to 4.5 weeks. Studies involving immune spleen cell transfer and treatment with antilymphocyte serum demonstrated the importance of cell-mediated immunity in HSV-2 infection. However, C. granulosum protection was not transferable with spleen cells from C. granulosum-treated animals nor was C. granulosum treatment capable of completely overcoming the increased mortality which resulted from antilymphocyte serum treatment of HSV-2 infected mice. Under our experimental conditions, silica did not affect the mortality in BALB/c mice due to HSV-2 but significantly reduced the protective effects induced by C. granulosum. Attempts to transfer protection of HSV-2 challenge in suckling mice by using either glass-adherent or mixed peritoneal cells from either HSV-2-immunized or C. granulosum-treated animals were unsuccessful.
AuthorsD A Gabrielson, J J Kelleher, J Varani
JournalInfection and immunity (Infect Immun) Vol. 30 Issue 3 Pg. 791-6 (Dec 1980) ISSN: 0019-9567 [Print] United States
PMID6262241 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Bacterial Vaccines
  • Immune Sera
  • Silicon Dioxide
Topics
  • Animals
  • Animals, Newborn
  • Bacterial Vaccines (administration & dosage, immunology)
  • Corynebacterium (immunology)
  • Immune Sera
  • Immunity, Cellular
  • Immunization
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Silicon Dioxide (immunology)
  • Simplexvirus (pathogenicity)
  • Spleen (immunology, transplantation)

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