Abstract
Experiments were performed to further elaborate on our congenital syphilis rabbit model. Attempts were made to determine whether in utero exposure to Treponema pallidum would stimulate immune reactivity and whether this activity would, in turn, affect lesion development upon challenge infection. Newborn rabbits aged 2 or 5 weeks were obtained from control does or from does infected intravenously with T. pallidum during pregnancy. Congenitally infected newborns exhibited increased immunologic functions. Concanavalin A-induced T-lymphocyte proliferation was elevated at both 2 and 5 weeks. In addition, macrophage Ia expression and RPR antibody titers were increased at 5 weeks. In separate experiments, newborn rabbits from control does or from does infected during pregnancy were challenged intradermally with viable organisms at either 2 or 5 weeks of age. Subsequent lesion severity was markedly increased in those newborns previously exposed to treponemes in utero. These observations further strengthen our model for congenital transmission of T. pallidum during pregnancy. We propose that at least some of the tissue pathology in syphilitic infection is associated with activated host defenses.
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Selected References
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- Chida K., Myrvik Q. N., Leake E. S., Gordon M. R., Wood P. H., Ricardo M. J., Jr Chemiluminescent responses of alveolar macrophages from normal and Mycobacterium bovis BCG-vaccinated rabbits as a function of age. Infect Immun. 1987 Jun;55(6):1476–1483. doi: 10.1128/iai.55.6.1476-1483.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dobson S. R., Taber L. H., Baughn R. E. Characterization of the components in circulating immune complexes from infants with congenital syphilis. J Infect Dis. 1988 Nov;158(5):940–947. doi: 10.1093/infdis/158.5.940. [DOI] [PubMed] [Google Scholar]
- Dobson S. R., Taber L. H., Baughn R. E. Recognition of Treponema pallidum antigens by IgM and IgG antibodies in congenitally infected newborns and their mothers. J Infect Dis. 1988 May;157(5):903–910. doi: 10.1093/infdis/157.5.903. [DOI] [PubMed] [Google Scholar]
- Fitzgerald T. J. Experimental congenital syphilis in rabbits. Can J Microbiol. 1985 Sep;31(9):757–762. doi: 10.1139/m85-142. [DOI] [PubMed] [Google Scholar]
- Fitzgerald T. J., Johnson R. C., Miller J. N., Sykes J. A. Characterization of the attachment of Treponema pallidum (Nichols strain) to cultured mammalian cells and the potential relationship of attachment to pathogenicity. Infect Immun. 1977 Nov;18(2):467–478. doi: 10.1128/iai.18.2.467-478.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gamboa D., Miller J. N. Experimental neonatal syphilis. I. Evidence of resistance to symptomatic infection in neonatal rabbits following intradermal inoculation with Treponema pallidum (Nichols strain). Pediatr Res. 1984 Oct;18(10):965–971. doi: 10.1203/00006450-198410000-00012. [DOI] [PubMed] [Google Scholar]
- Gamboa D., Miller J. N., Lukehart S. A., Baker-Zander S. A., Sell S. Experimental neonatal syphilis. II. Immunological responses of neonatal rabbits to intradermal inoculation with Treponema pallidum (Nichols strain). Pediatr Res. 1984 Oct;18(10):972–979. doi: 10.1203/00006450-198410000-00013. [DOI] [PubMed] [Google Scholar]
- Lobel S. A., Knight K. L. The role of rabbit Ia molecules in immune functions as determined with the use of an anti-Ia monoclonal antibody. Immunology. 1984 Jan;51(1):35–43. [PMC free article] [PubMed] [Google Scholar]
- Lukehart S. A., Baker-Zander S. A., Lloyd R. M., Sell S. Effect of cortisone administration on host-parasite relationships in early experimental syphilis. J Immunol. 1981 Oct;127(4):1361–1368. [PubMed] [Google Scholar]
- Meyer M. P., Malan A. F. Rheumatoid factor in the diagnosis of congenital syphilis. S Afr Med J. 1987 Nov 21;72(10):668–669. [PubMed] [Google Scholar]
- Sherman M. P., Lehrer R. I. Oxidative metabolism of neonatal and adult rabbit lung macrophages stimulated with opsonized group B streptococci. Infect Immun. 1985 Jan;47(1):26–30. doi: 10.1128/iai.47.1.26-30.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sherman M. P., Lehrer R. I. Superoxide generation by neonatal and adult rabbit alveolar macrophages. J Leukoc Biol. 1984 Jul;36(1):39–50. doi: 10.1002/jlb.36.1.39. [DOI] [PubMed] [Google Scholar]
- Sherman M., Goldstein E., Lippert W., Wennberg R. Neonatal lung defense mechanisms: a study of the alveolar macrophage system in neonatal rabbits. Am Rev Respir Dis. 1977 Sep;116(3):433–440. doi: 10.1164/arrd.1977.116.3.433. [DOI] [PubMed] [Google Scholar]
- Takata I., Gordon M. R., Myrvik Q. N. Demonstration of a macrophage migration enhancement factor in the sera of young rabbits. Cell Immunol. 1985 Oct 1;95(1):137–145. doi: 10.1016/0008-8749(85)90302-8. [DOI] [PubMed] [Google Scholar]
- Tomai M. A., Elmquist B. J., Warmka S. M., Fitzgerald T. J. Macrophage-mediated suppression of con A-induced IL-2 production in spleen cells from syphilitic rabbits. J Immunol. 1989 Jul 1;143(1):309–314. [PubMed] [Google Scholar]
- Zeligs B. J., Nerurkar L. S., Bellanti J. A. Chemotactic and candidacidal responses of rabbit alveolar macrophages during postnatal development and the modulating roles of surfactant in these responses. Infect Immun. 1984 May;44(2):379–385. doi: 10.1128/iai.44.2.379-385.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zeligs B. J., Nerurkar L. S., Bellanti J. A. Maturation of the rabbit alveolar macrophage during animal development. III. Phagocytic and bactericidal functions. Pediatr Res. 1977 Dec;11(12):1208–1211. doi: 10.1203/00006450-197712000-00008. [DOI] [PubMed] [Google Scholar]