Literature DB >> 6424446

Protective activity of an intravenous immune globulin (human) enriched in antibody against lipopolysaccharide antigens of Pseudomonas aeruginosa.

M S Collins, R E Roby.   

Abstract

Human plasmas containing naturally high levels of immunoglobulin G (IgG) to lipopolysaccharide antigens of Pseudomonas aeruginosa immunotypes 1, 2, 4, and 6 were identified by an enzyme-linked immunosorbent assay. The high titered plasmas were collected, pooled, and fractionated. Cohn fraction II IgG was prepared for intravenous infusion. The antibody titers in the hyperimmune intravenous immunoglobulin preparation were approximately fivefold higher against P. aeruginosa immunotypes 1, 2, 4, 5, and 6 and approximately twofold higher against immunotypes 3 and 7 than conventional intravenous immunoglobulin G. When tested for prophylaxis in burned mice, the protective doses 50 percent of Pseudomonas-intravenous immunoglobulin G were approximately fourfold less effective against immunotypes 1, 2, 4, and 7 and International Antigenic Typing System Serotypes (IATS), 8 (= immunotype 6) than conventional intravenous immunoglobulin G. Against immunotype 3 and 5, IATS 13, 15, and 16, both immunoglobulin preparations afforded similar levels of protection. In burned mice challenged with immunotypes 1 and 2 and not treated until 18 hours after infection, Pseudomonas-intravenous immunoglobulin G and tobramycin had synergistic activity in preventing death. Pseudomonas-intravenous immunoglobulin G also afforded significant protection to immunosuppressed mice challenged with immunotype 1. These data suggest that Pseudomonas-intravenous immunoglobulin G may be useful in prevention or treatment of P. aeruginosa infections in man.

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Year:  1984        PMID: 6424446     DOI: 10.1016/0002-9343(84)90337-1

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


  27 in total

Review 1.  Immunological perspectives in prevention and treatment of nosocomial pneumonia.

Authors:  J E Pennington
Journal:  Intensive Care Med       Date:  1992       Impact factor: 17.440

2.  Polyclonal and monoclonal antibody therapy for experimental Pseudomonas aeruginosa pneumonia.

Authors:  J E Pennington; G J Small; M E Lostrom; G B Pier
Journal:  Infect Immun       Date:  1986-10       Impact factor: 3.441

3.  [Lipopolysaccharides, endotoxins and O-antigens of gram-negative bacteria: chemical structure, biologic effect and serologic properties].

Authors:  E T Rietschel; H Brade
Journal:  Infection       Date:  1987 Mar-Apr       Impact factor: 3.553

4.  Pseudomonas aeruginosa immunotherapy.

Authors:  J E Pennington
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1990-06       Impact factor: 3.267

Review 5.  Immunotherapy of infectious diseases: past, present and future.

Authors:  J E Pennington
Journal:  Trans Am Clin Climatol Assoc       Date:  1988

Review 6.  Recent developments for Pseudomonas vaccines.

Authors:  Anurag Sharma; Anja Krause; Stefan Worgall
Journal:  Hum Vaccin       Date:  2011-10-01

7.  [Lipopolysaccharides, endotoxins and O-antigens of gram-negative bacteria: chemical structure, biologic effect and serologic properties].

Authors:  E T Rietschel; H Brade
Journal:  Infection       Date:  1987       Impact factor: 3.553

8.  Smooth lipopolysaccharide is the major protective antigen for mice in the surface extract from IATS serotype 6 contributing to the polyvalent Pseudomonas aeruginosa vaccine PEV.

Authors:  S MacIntyre; R Lucken; P Owen
Journal:  Infect Immun       Date:  1986-04       Impact factor: 3.441

9.  Intravitreal human immune globulin in a rabbit model of Staphylococcus aureus toxin-mediated endophthalmitis: a potential adjunct in the treatment of endophthalmitis.

Authors:  Dennis P Han
Journal:  Trans Am Ophthalmol Soc       Date:  2004

10.  Nonopsonic antibodies in cystic fibrosis. Pseudomonas aeruginosa lipopolysaccharide-specific immunoglobulin G antibodies from infected patient sera inhibit neutrophil oxidative responses.

Authors:  I Eichler; L Joris; Y P Hsu; J Van Wye; R Bram; R Moss
Journal:  J Clin Invest       Date:  1989-12       Impact factor: 14.808

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