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.
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Authors | D A Gabrielson, J J Kelleher, J Varani |
Journal | Infection and immunity
(Infect Immun)
Vol. 30
Issue 3
Pg. 791-6
(Dec 1980)
ISSN: 0019-9567 [Print] United States |
PMID | 6262241
(Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Bacterial Vaccines
- Immune Sera
- Silicon Dioxide
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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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