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Vaccine Detail
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Brucella abortus O-polysaccharide subunit vaccine |
| Vaccine Information |
- Vaccine Name: Brucella abortus O-polysaccharide subunit vaccine
- Target Pathogen: Brucella spp.
- Target Disease: Brucellosis
- Vaccine Ontology ID: VO_0009064
- Type: Subunit vaccine
- Status: Research
- Host Species for Licensed Use: Pig
- Host Species as Laboratory Animal Model: Mus musculus (CD-1 outbred mice); mouse peritoneal macrophages
- Antigen: O polysaccharide | O-polysaccharide (OPS)
- Preparation: Passive administration of O polysaccharide-specific IgG2a and IgG1 monoclonal antibodies and convalescent-phase serum. (Winter et al, 1989)
Purified O-polysaccharide at doses of 100 to 500 micrograms; administered intramuscularly or orally; one or three doses. (Lord et al, 1998)
- Description: The study investigated whether antibody alone could prevent infection with Brucella abortus by using monoclonal antibodies specific to the O polysaccharide. Efficacy: 82% of mice infected with 100 CFU of B. abortus preincubated with IgG2a MAb were free of infection up to 6 weeks; higher challenge doses reduced efficacy; IgG1 MAb and convalescent serum diminished but did not prevent infection. Immune response: Antibodies of appropriate specificity and isotype (IgG2a) were effective in opsonizing B. abortus and facilitating killing by activated macrophages; killing required activated macrophages and endotoxin presence in medium. (Winter et al, 1989)
Purified OPS from Brucella abortus 1119-3 and Brucella suis 1330 were evaluated as vaccines in field trials in Venezuela for protection of swine against Brucella suis challenge. Efficacy: Gilts vaccinated with OPS showed no serologic reactions, no abortions (100% protection), and litter sizes of 10 to 12 pigs. Immune response: No serologic reactions detected in vaccinated gilts, indicating effective protection without detectable antibody response by the assays used. (Lord et al, 1998)
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| Host Response |
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Mouse Response
- Host Strain: CD-1
- Host cell type: macrophages
- Immune Response: Antibodies of appropriate specificity and isotype (IgG2a) were effective in opsonizing B. abortus and facilitating killing by activated macrophages; killing required activated macrophages and endotoxin presence in medium. (Winter et al, 1989)
- Efficacy: 82% of mice infected with 100 CFU of B. abortus preincubated with IgG2a MAb were free of infection up to 6 weeks; higher challenge doses reduced efficacy; IgG1 MAb and convalescent serum diminished but did not prevent infection. (Winter et al, 1989)
- Description: Mice were infected with virulent Brucella abortus 2308 preincubated with graded quantities of O polysaccharide-specific monoclonal antibodies; in vitro opsonization and killing assays with mouse peritoneal macrophages were also performed. (Winter et al, 1989)
Pig Response
- Immune Response: No serologic reactions detected in vaccinated gilts, indicating effective protection without detectable antibody response by the assays used. (Lord et al, 1998)
- Challenge Protocol: Purified OPS from Brucella abortus 1119-3 and Brucella suis 1330 were evaluated as vaccines in field trials in Venezuela for protection of swine against Brucella suis challenge. (Lord et al, 1998)
- Efficacy: Gilts vaccinated with OPS showed no serologic reactions, no abortions (100% protection), and litter sizes of 10 to 12 pigs. (Lord et al, 1998)
- Description: Vaccination of gilts, mating with infected boars, followed by serologic testing, bacteriologic culture, abortion monitoring, and litter size assessment. (Lord et al, 1998)
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| References |
Lord et al, 1998: Lord VR, Cherwonogrodzky JW, Schurig GG, Lord RD, Marcano MJ, Meléndez GE. Venezuelan field trials of vaccines against brucellosis in swine. American journal of veterinary research. 1998 May; 59(5); 546-51. [PubMed: 9582954].
Winter et al, 1989: Winter AJ, Duncan JR, Santisteban CG, Douglas JT, Adams LG. Capacity of passively administered antibody to prevent establishment of Brucella abortus infection in mice. Infection and immunity. 1989 Nov; 57(11); 3438-44. [PubMed: 2509362].
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