» Articles » PMID: 2471694

Specific Immunological Unresponsiveness to Bacterial Lipopolysaccharides Develops in a Cyclic Manner

Overview
Journal Infect Immun
Date 1989 Jul 1
PMID 2471694
Citations 1
Authors
Affiliations
Soon will be listed here.
Abstract

Prior exposure (priming) of BALB/cByJ mice to a low dose of lipopolysaccharide derived from Escherichia coli 055 or Serratia marcescens, followed by immunization with an optimally immunogenic dose of the same lipopolysaccharide 2 to 30 days later, results in the expression of substantially reduced antibody responses. Such unresponsiveness, which is antigen specific, occurs in a cyclic manner with time after priming.

Citing Articles

Toxicity and immunogenicity of Neisseria meningitidis lipopolysaccharide incorporated into liposomes.

Petrov A, SEMENOV B, Vartanyan Y, Zakirov M, Torchilin V, Trubetskoy V Infect Immun. 1992; 60(9):3897-903.

PMID: 1500196 PMC: 257405. DOI: 10.1128/iai.60.9.3897-3903.1992.

References
1.
Britton S, Wepsic T, Moller G . Persistence of immunogenicity of two complex antigens retained in vivo. Immunology. 1968; 14(4):491-501. PMC: 1409385. View

2.
Elkins K, STASHAK P, Baker P . Mechanisms of specific immunological unresponsiveness to bacterial lipopolysaccharides. Infect Immun. 1987; 55(12):3093-102. PMC: 260033. DOI: 10.1128/iai.55.12.3093-3102.1987. View

3.
Baker P, STASHAK P . Quantitative and qualitative studies on the primary antibody response to pneumococcal polysaccharides at ehe cellular level. J Immunol. 1969; 103(6):1342-8. View

4.
Gottlieb C . Application of transformations to normalize the distribution of plaque-forming cells. J Immunol. 1974; 113(1):51-7. View

5.
Von Eschen K, Rudbach J . Immunological responses of mice to native protoplasmic polysaccharide and lipopolysaccharide: functional separation of the two signals required to stimulate a secondary antibody response. J Exp Med. 1974; 140(6):1604-14. PMC: 2139752. DOI: 10.1084/jem.140.6.1604. View