» Articles » PMID: 6698608

Protection Against Fatal Pseudomonas Aeruginosa Burn Wound Sepsis by Immunization with Lipopolysaccharide and High-molecular-weight Polysaccharide

Overview
Journal Infect Immun
Date 1984 Mar 1
PMID 6698608
Citations 26
Authors
Affiliations
Soon will be listed here.
Abstract

A murine burn wound model was employed to evaluate the relative efficacy of purified Pseudomonas aeruginosa lipopolysaccharide (LPS) and high-molecular-weight polysaccharide as protective immunogens. LPS was found to be both highly immunogenic and protective. As little as three 0.001-microgram doses elicited good immunoglobulin M and G titers and increased the mean lethal dose more than 1,000-fold. The level of protection against a live challenge correlated with antibody titers and was found to be serotype specific. An immunizing regimen which evoked only an immunoglobulin M response was still found to offer substantial protection. Immunization with a high-molecular-weight polysaccharide was also found to be protective. However, approximately 1,000-fold more high-molecular-weight polysaccharide, as compared with LPS, was needed to protect mice to an equivalent degree. Immunization with LPS was found to promote bacterial clearance and prevent establishment of bacteremia. A multivalent LPS vaccine conferred high levels of protection (110- to 53,000-fold) against eight different challenge strains of various serotypes.

Citing Articles

Construction of a Protective Vaccine Against Lipopolysaccharide-Heterologous Strains Based on Expression Profiling of Outer Membrane Proteins During Infection.

Liu C, Pan X, Xia B, Chen F, Jin Y, Bai F Front Immunol. 2018; 9:1737.

PMID: 30093906 PMC: 6070602. DOI: 10.3389/fimmu.2018.01737.


Pseudomonas aeruginosa PAO-1 Lipopolysaccharide-Diphtheria Toxoid Conjugate Vaccine: Preparation, Characterization and Immunogenicity.

Najafzadeh F, Shapouri R, Rahnema M, Rokhsartalab Azar S, Kianmehr A Jundishapur J Microbiol. 2015; 8(6):e17712.

PMID: 26301059 PMC: 4541022. DOI: 10.5812/jjm.8(5)2015.17712.


Vaccines for Pseudomonas aeruginosa: a long and winding road.

Priebe G, Goldberg J Expert Rev Vaccines. 2014; 13(4):507-19.

PMID: 24575895 PMC: 4521563. DOI: 10.1586/14760584.2014.890053.


Fms-like tyrosine kinase-3 ligand alters antigen-specific responses to infections after severe burn injury.

Bohannon J, Fang G, Cui W, Sherwood E, Toliver-Kinsky T Shock. 2009; 32(4):435-41.

PMID: 19752689 PMC: 3100155. DOI: 10.1097/SHK.0b013e31819e2937.


Active immunization using exotoxin A confers protection against Pseudomonas aeruginosa infection in a mouse burn model.

Manafi A, Kohanteb J, Mehrabani D, Japoni A, Amini M, Naghmachi M BMC Microbiol. 2009; 9:23.

PMID: 19183501 PMC: 2644702. DOI: 10.1186/1471-2180-9-23.


References
1.
PAVLOVSKIS O, Edman D, Leppla S, Wretlind B, Lewis L, Martin K . Protection against experimental Pseudomonas aeruginosa infection in mice by active immunization with exotoxin A toxoids. Infect Immun. 1981; 32(2):681-9. PMC: 351501. DOI: 10.1128/iai.32.2.681-689.1981. View

2.
Okada K, Kawaharajo K, Kasai T, HOMMA J . Effects of somatic component of Pseudomonas aeruginosa on protective immunity in experimental mouse burn infection. Jpn J Exp Med. 1980; 50(1):53-61. View

3.
Pennington J, Hickey W, Blackwood L, Arnaut M . Active immunization with lipopolysaccharide Pseudomonas antigen for chronic Pseudomonas bronchopneumonia in guinea pigs. J Clin Invest. 1981; 68(5):1140-8. PMC: 370907. DOI: 10.1172/jci110358. View

4.
Stieritz D, Holder I . Experimental studies of the pathogenesis of infections due to Pseudomonas aeruginosa: description of a burned mouse model. J Infect Dis. 1975; 131(6):688-91. DOI: 10.1093/infdis/131.6.688. View

5.
Pier G, Sidberry H, Sadoff J . Protective immunity induced in mice by immunization with high-molecular-weight polysaccharide from Pseudomonas aeruginosa. Infect Immun. 1978; 22(3):919-25. PMC: 422244. DOI: 10.1128/iai.22.3.919-925.1978. View