Literature DB >> 6799587

Type-specific vs. cross-protective vaccination for gram-negative bacterial pneumonia.

J E Pennington, E Menkes.   

Abstract

Groups of guinea pigs received four injections intramuscularly of lipopolysaccharide vaccine derived from Pseudomonas aeruginosa, cross-protective core glycolipid vaccine derived from the J-5 mutant of Escherichia coli O111, or saline during a two-week period. Titers of passive hemagglutinating antibody to vaccine antigens in serum routinely increased fourfold or more. Experimental hemorrhagic pseudomonas pneumonia was then induced, from which the rates of survival were 15% among animals receiving saline, 81% among animals receiving pseudomonas vaccine (P less than 0.001), and 42% among animals receiving J-5 vaccine. Thus, only weak cross-protection against pseudomonas pneumonia was detected in the recipients of J-5 vaccine. Further studies revealed no protection against pneumonia due to either E. coli or Klebsiella in animals receiving J-5 vaccine. From these data, species-specific vaccination appears to be superior to vaccination with cross-protective antigen against experimental pseudomonas pneumonia.

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Year:  1981        PMID: 6799587     DOI: 10.1093/infdis/144.6.599

Source DB:  PubMed          Journal:  J Infect Dis        ISSN: 0022-1899            Impact factor:   5.226


  13 in total

Review 1.  Bloodstream infections: epidemiology, pathophysiology and therapeutic perspectives.

Authors:  R Salomão; O Rigato; A C Pignatari; M A Freudenberg; C Galanos
Journal:  Infection       Date:  1999 Jan-Feb       Impact factor: 3.553

Review 2.  Immunological perspectives in prevention and treatment of nosocomial pneumonia.

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

3.  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

Review 4.  Immunotherapeutic advances in the treatment of gram-negative bacterial sepsis.

Authors:  D L Dunn
Journal:  World J Surg       Date:  1987-04       Impact factor: 3.352

5.  Protection of mice against the lethal toxicity of a lipopolysaccharide (LPS) by immunization with anti-idiotype antibody to a monoclonal antibody to lipid A from Eikenella corrodens LPS.

Authors:  T Kato; I Takazoe; K Okuda
Journal:  Infect Immun       Date:  1990-02       Impact factor: 3.441

6.  Isolation and characterization of a human monoclonal antibody that recognizes epitopes shared by Pseudomonas aeruginosa immunotype 1, 3, 4, and 6 lipopolysaccharides.

Authors:  A B Lang; E Fürer; J W Larrick; S J Cryz
Journal:  Infect Immun       Date:  1989-12       Impact factor: 3.441

7.  Monoclonal antibodies specific for Escherichia coli J5 lipopolysaccharide: cross-reaction with other gram-negative bacterial species.

Authors:  L M Mutharia; G Crockford; W C Bogard; R E Hancock
Journal:  Infect Immun       Date:  1984-09       Impact factor: 3.441

8.  Antibody specific for Escherichia coli J5 cross-reacts to various degrees with an Escherichia coli clinical isolate grown for different lengths of time.

Authors:  D E McCallus; N L Norcross
Journal:  Infect Immun       Date:  1987-05       Impact factor: 3.441

9.  Isolation and characterization of murine monoclonal antibodies specific for gram-negative bacterial lipopolysaccharide: association of cross-genus reactivity with lipid A specificity.

Authors:  W C Bogard; D L Dunn; K Abernethy; C Kilgarriff; P C Kung
Journal:  Infect Immun       Date:  1987-04       Impact factor: 3.441

10.  Reactivity of the human antiendotoxin immunoglobulin M monoclonal antibody HA-1A with lipopolysaccharides from rough and smooth gram-negative organisms.

Authors:  M A Mascelli; B Frederick; T Ely; D S Neblock; D J Shealy; K Y Pak; P E Daddona
Journal:  Infect Immun       Date:  1993-05       Impact factor: 3.441

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