Abstract
Mice not normally susceptible to infection with Leptospira interrogans serovar pomona were rendered susceptible to lethal infections by treatment with a single dose of 300 mg of cyclophosphamide (Cy) per kg administered optimally from 4 days before to 1 day after infection. Cy-treated mice with either passively or actively acquired antibody were protected from death. Blood levels of leptospires in infected untreated and in Cy-treated mice remained similar until 2 days after infection, when untreated mice cleared the leptospires. Soon afterwards, opsonizing and agglutinating antibody appeared. Cy-treated mice given spleen cells from other normal or specifically immune mice were protected from infection. An important factor in the natural resistance of mice to leptospiral infection appears to be their capacity to produce circulating antibody within 48 to 72 h. Applications are suggested for this animal model in vaccination and protection studies.
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Selected References
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- Barron L. D. Parity and optical activity. Nature. 1972 Jul 7;238(5358):17–19. doi: 10.1038/238017a0. [DOI] [PubMed] [Google Scholar]
- Camenga D. L., Nathanson N., Cole G. A. Cyclophosphamide-potentiated West Nile viral encephalitis: relative influence of cellular and humoral factors. J Infect Dis. 1974 Dec;130(6):634–641. doi: 10.1093/infdis/130.6.634. [DOI] [PubMed] [Google Scholar]
- Canonico P. G., McManus A. T., Mangiafico J. A., Sammons L. S., McGann V. G., Dangerfield H. G. Temporal appearance of opsonizing antibody to Francisella tularensis: detection by a radiometabolic assay. Infect Immun. 1975 Mar;11(3):466–469. doi: 10.1128/iai.11.3.466-469.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Christmas B. W., Bragger J. M., Till D. G. Dairy farm fever in New Zealand: isolation of L pomona and L hardjo from a local outbreak. N Z Med J. 1974 May 8;79(514):904–906. [PubMed] [Google Scholar]
- Cozad G. C., Lindsey T. J. Effect of cyclophosphamide on Histoplasma capsulatum infections in mice. Infect Immun. 1974 Feb;9(2):261–265. doi: 10.1128/iai.9.2.261-265.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- FAINE S. RETICULOENDOTHELIAL PHAGOCYTOSIS OF VIRULENT LEPTOSPIRES. Am J Vet Res. 1964 May;25:830–835. [PubMed] [Google Scholar]
- FRISCH A. W., DAVIES G. H. INHIBITION OF HEMAGGLUTININ SYNTHESIS BY CYTOXAN. Cancer Res. 1965 Jun;25:745–751. [PubMed] [Google Scholar]
- Haranaka K., Sugane K., Mashimo K. Combination therapy of anti-endotoxin antibody and gentamicin in the immunosuppressed mice with Pseudomonas aeruginosa infection. Jpn J Exp Med. 1975 Jun;45(3):207–213. [PubMed] [Google Scholar]
- Hurd J., Heath R. B. Effect of cyclophosphamide on infections in mice caused by virulent and avirulent strains of influenza virus. Infect Immun. 1975 May;11(5):886–889. doi: 10.1128/iai.11.5.886-889.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kerckhaert J. A., Van den Berg G. J., Willers J. M. Influence of cyclophosphamide on the delayed hypersensitivity of the mouse. Ann Immunol (Paris) 1974 Mar-Apr;125(3):415–426. [PubMed] [Google Scholar]
- Kline I., Gang M., Tyrer D. D., Mantel N., Venditti J. M., Goldin A. Duration of drug levels in mice as indicated by residual antileukemic efficacy. Chemotherapy. 1968;13(1):28–41. doi: 10.1159/000220528. [DOI] [PubMed] [Google Scholar]
- Rager-Zisman B., Allison A. C. Effects of immunosuppression on coxsackie B-3 virus infection in mice, and passive protection by circulating antibody. J Gen Virol. 1973 Jun;19(3):339–351. doi: 10.1099/0022-1317-19-3-339. [DOI] [PubMed] [Google Scholar]
- Singer S. H., Ford M., Kirschstein R. L. Respiratory diseases in cyclophosphamide-treated mice. I. Increased virulence of Mycoplasma pulmonis. Infect Immun. 1972 Jun;5(6):953–956. doi: 10.1128/iai.5.6.953-956.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stockman G. D., Heim L. R., South M. A., Trentin J. J. Differential effects of cyclophosphamide on the B and T cell compartments of adult mice. J Immunol. 1973 Jan;110(1):277–282. [PubMed] [Google Scholar]
- Tachibana N., Kobayashi V. Effect of cyclophosphamide on the growth of Rickettsia sennetsu in experimentally infected mice. Infect Immun. 1975 Sep;12(3):625–629. doi: 10.1128/iai.12.3.625-629.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tripathy S. P., Mackaness G. B. The effect of cytotoxic agents on the passive transfer of cell-mediated immunity. J Exp Med. 1969 Jul 1;130(1):17–30. doi: 10.1084/jem.130.1.17. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Turk J. L., Parker D., Poulter L. W. Functional aspects of the selective depletion of lymphoid tissue by cyclophosphamide. Immunology. 1972 Oct;23(4):493–501. [PMC free article] [PubMed] [Google Scholar]
- Turk J. L., Poulter L. W. Selective depletion of lymphoid tissue by cyclophosphamide. Clin Exp Immunol. 1972 Feb;10(2):285–296. [PMC free article] [PubMed] [Google Scholar]
- Worthington M., Rabson A. S., Baron S. Mechanism of recovery from systemic vaccinia virus infection. I. The effects of cyclophosphamide. J Exp Med. 1972 Aug 1;136(2):277–290. doi: 10.1084/jem.136.2.277. [DOI] [PMC free article] [PubMed] [Google Scholar]
