Abstract
Immunosuppression by cyclophosphamide was used to make mice incapable of B-lymphocyte responses; they could not make an antibody response to NIP-Ficoll. These mice, as well as untreated mice, were challenged intraperitoneally with graded doses of isogenic O-4,12 or O-6,7 Salmonella typhimurium derivatives. The 50% lethal dose of the O-6,7 strains was 35- to 70-fold higher than that of the O-4,12 strains, both in the normal and the immunosuppressed animals, although the latter were approximately 1,000-fold more susceptible to the infection by either challenge organism. We conclude that the O-antigen-dependent difference in the mouse virulence of these sister strains is not mediated through differences in their capacity to evoke B-lymphocyte-mediated immune responses.
Full text
PDF


Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Collins F. M. Mechanisms in antimicrobial immunity. J Reticuloendothel Soc. 1971 Jul;10(1):58–99. [PubMed] [Google Scholar]
- Gadeberg O. V., Rhodes J. M., Larsen S. O. The effect of various immunosuppressive agents on mouse peritoneal macrophages and on the in vitro phagocytosis of Escherichia coli O4:K3:H5 and degradation of 125I-labelled HSA-antibody complexes by these cells. Immunology. 1975 Jan;28(1):59–70. [PMC free article] [PubMed] [Google Scholar]
- Hochadel J. F., Keller K. F. Protective effects of passively transferred immune T- or B-lymphocytes in mice infected with Salmonella typhimurium. J Infect Dis. 1977 May;135(5):813–823. doi: 10.1093/infdis/135.5.813. [DOI] [PubMed] [Google Scholar]
- Hurme M. Immunological memory after priming with a thymus independent antigen, NIP-ficoll. 4-hydroxy-5-iodo-3-nitrophenylacetyl coupled to polymer of sucrose and epichlorhydrin. Acta Pathol Microbiol Scand C. 1976 Oct;84C(5):345–352. [PubMed] [Google Scholar]
- JENKIN C. R., ROWLEY D. BASIS FOR IMMUNITY TO TYPHOID IN MICE AND THE QUESTION OF "CELLULAR IMMUNITY". Bacteriol Rev. 1963 Dec;27:391–404. doi: 10.1128/br.27.4.391-404.1963. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Morris J. A., Wray C., Sojka W. J. The effect of T and B lymphocyte depletion on the protection of mice vaccinated with a Gal E mutant of Salmonella typhimurium. Br J Exp Pathol. 1976 Jun;57(3):354–360. [PMC free article] [PubMed] [Google Scholar]
- Mäkelä P. H., Valtonen V. V., Valtonen M. Role of O-antigen (lipopolysaccharide) factors in the virulence of Salmonella. J Infect Dis. 1973 Jul;128(Suppl):81–85. doi: 10.1093/infdis/128.supplement_1.s81. [DOI] [PubMed] [Google Scholar]
- Smith R. A., Bigley N. J. Detection of delayed hypersensitivity in mice injected with ribonucleic acid-protein fractions of Salmonella typhimurium. Infect Immun. 1972 Sep;6(3):384–389. doi: 10.1128/iai.6.3.384-389.1972. [DOI] [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]
- Valtonen M. V., Larinkari U. M., Plosila M., Valtonen V. V., Mäkelä P. H. Effect of enterobacterial common antigen on mouse virulence of Salmonella typhimurium. Infect Immun. 1976 Jun;13(6):1601–1605. doi: 10.1128/iai.13.6.1601-1605.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Valtonen M. V., Plosila M., Valtonen V. V., Mäkelä P. H. Effect of the quality of the lipopolysaccharide on mouse virulence of Salmonella enteritidis. Infect Immun. 1975 Oct;12(4):828–832. doi: 10.1128/iai.12.4.828-832.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Valtonen V. V. Mouse virulence of Salmonella strains: the effect of different smooth-type O side-chains. J Gen Microbiol. 1970 Dec;64(3):255–268. doi: 10.1099/00221287-64-3-255. [DOI] [PubMed] [Google Scholar]
- Willers J. M., Sluis E. The influence of cyclophosphamide on antibody formation in the mouse. Ann Immunol (Paris) 1975 Apr;126(3):267–279. [PubMed] [Google Scholar]
