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.
MeSH Terms
Animals
Antibody Formation
Antigens, Bacterial
B-Lymphocytes/drug effects
Cyclophosphamide/pharmacology
Disease Models, Animal
Ficoll/analogs & derivatives,immunology
Hybridization, Genetic
Immunosuppression Therapy
Mice
Salmonella/immunology
Salmonella Infections/immunology
Salmonella typhimurium/pathogenicity
Virulence
Chemicals
Antigens, Bacterial
Ficoll
Cyclophosphamide
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Valtonen M V
Häyry P
References (13)
13 references, click to expand
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