Role of Nonagglutinating Antibody in the Protracted Immunity of Vaccinated Mice to Pseudomonas aeruginosa Infection
Autor: | P. Fiset, V. M. Young, R. W. I. Kessel, M. R. Moody |
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Rok vydání: | 1978 |
Předmět: |
Blood Bactericidal Activity
Immunology Microbiology Immunoglobulin G Mice Agglutinin Pseudomonas infection Immunity medicine Animals Pseudomonas Infections Mice Inbred C3H biology Vaccination Immunization Passive medicine.disease Antibodies Bacterial Titer Infectious Diseases Immunoglobulin M Immunization Agglutinins Pseudomonas aeruginosa biology.protein Female Parasitology Antibody Immunologic Memory |
Zdroj: | Infection and Immunity. 21:905-913 |
ISSN: | 1098-5522 0019-9567 |
DOI: | 10.1128/iai.21.3.905-913.1978 |
Popis: | Effective immunization against infection with Pseudomonas aeruginosa is difficult to evaluate because agglutinin levels decline rapidly. Because fractionation of hyperimmune sera often yields more specific antibody than can be accounted for by direct agglutination tests, an immunoglobulin-specific assay based on antiglobulin augmentation was used to characterize antibody responses of C3H/HeJ mice vaccinated with P. aeruginosa type 2 lipopolysaccharide. Nonagglutinating antibodies, initially detected at 2 weeks post-primary vaccination, were predominantly immunoglobulin G after 5 weeks, and they remained elevated at levels usually 32-fold higher than the direct titer throughout the 4-month study period. The sequential production of immunoglobulin M, then immunoglobulin G, followed that found in orthodox immunological responses. Sera that contained nonagglutinating antibodies but not direct agglutinins (14 to 16 weeks) enhanced phagocytosis of P. aeruginosa type 2 by macrophages from unimmunized mice and passively immunized mice against lethal challenge doses; bactericidal activity of these sera was not demonstrated in the presence or absence of complement. When challenged with 1, 10, and 100 50% lethal doses at 16 weeks, survival rates of actively immunized mice were significantly higher than those of unvaccinated mice ( P < 0.001). Thus, at a time when no direct agglutinins were detectable, the augmented system detected nonagglutinating antibodies that could confer protracted resistance in vaccinated mice to pseudomonas infection. |
Databáze: | OpenAIRE |
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