Abstract
Serum IgM immunoglobulin levels and antibody responses to an optimally immunogenic dose of Type III pneumococcal polysaccharide (SSS-III) were assessed for F(1), F(2), and backcross progeny derived from crosses between high responding BALB/cAnN (B) and low responding CBA/HN (C) mice. The results obtained confirmed our original hypothesis, namely, that a major component, present on the X chromosome, governs the ability to respond to SSS-III in a decisive manner. Although all low responding C mice had low IgM levels, both intermediate and high responders had high IgM levels of the same magnitude. Treatment with bacterial lipopolysaccharides (LPS) resulted in a significant increase in the IgM levels of low responding C mice. While the IgM levels attained were similar to those of high responding B mice, not given LPS, no antibody specific for LPS appeared to be produced. These findings suggest that C mice are unable to make an IgM antibody response to SSS-III and other polysaccharide antigens, despite the fact that they possess the capacity to synthesize normal amounts of IgM immunoglobulin.
MeSH Terms
Animals
Antibodies, Bacterial
Antibody Formation
Antigens, Bacterial
Crosses, Genetic
Escherichia coli/immunology
Female
Hemolysis
Hemolytic Plaque Technique
Immunization
Immunogenetics
Immunoglobulin M
Lipopolysaccharides
Male
Mice
Mice, Inbred BALB C
Mice, Inbred CBA
Polysaccharides, Bacterial
Salmonella typhi/immunology
Salmonella typhimurium/immunology
Serratia marcescens/immunology
Sex Chromosomes
Streptococcus pneumoniae/immunology
Chemicals
Antibodies, Bacterial
Antigens, Bacterial
Immunoglobulin M
Lipopolysaccharides
Polysaccharides, Bacterial
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Amsbaugh D F
Hansen C T
Prescott B
Stashak P W
Asofsky R
Baker P J
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