Evaluation of a commercially available hyperimmune plasma product for prevention of naturally acquired pneumonia caused by Rhodococcus equi in foals.
- Clinical Trial
- Journal Article
- Randomized Controlled Trial
- Research Support
- Non-U.S. Gov't
Summary
This is a study to evaluate how effective a commercial hyperimmune plasma product is at preventing pneumonia caused by the bacterium Rhodococcus equi in foals. The study found no significant difference in pneumonia incidence among foals given this plasma product compared to those untreated.
Methods
- The study was a randomized clinical trial involving 165 foals.
- These foals were divided into two groups. One group received hyperimmune plasma, while the other acted as nontreated controls.
- Foals with a failure of passive transfer (FPT) of immunity, meaning they did not receive sufficient antibodies from their mothers’ colostrum, were also treated with hyperimmune plasma and analyzed as a distinct group.
- The foals that received the plasma were treated with doses of 950 ml, once between when they were 1 to 10 days old and again when they were 30 to 50 days old.
- A tracheobronchial aspirate, a fluid sample from the respiratory tract, was obtained from any foals showing respiratory symptoms. This was then cultured for bacteria to confirm the presence of Rhodococcus equi.
Results
- The study found no significant difference in the incidence of R. equi-caused pneumonia between the foals given the plasma (19.1%) and the untreated control foals (30%).
- Of the 13 foals with FPT that received plasma and developed pneumonia, 12 did so before the administration of the second dose of hyperimmune plasma.
- The overall incidence of pneumonia from all causes did not differ between the two groups.
Conclusions
- The intravenous administration of the commercially available hyperimmune plasma product was deemed safe and was shown to contain high concentrations of anti-R. equi antibodies.
- However, in this particular group of foals, the difference in the occurrence of pneumonia caused by R. equi between those that received plasma and those left untreated was not significant.
The findings suggest that while this hyperimmune plasma product is safe and rich in anti-R. equi antibodies, it did not significantly reduce the incidence of R. equi-caused pneumonia within the sampled group of foals. The reasons for this weren’t outlined in the abstract, but it may require further research to better understand the effects of hyperimmune plasma on foals’ susceptibility to this bacterium.
Cite This Article
Publication
Researcher Affiliations
- Department of Large Animal Clinical Sciences, College of Veterinary Medicine, University of Florida, Gainesville, FL 32610, USA.
MeSH Terms
- Actinomycetales Infections / immunology
- Actinomycetales Infections / prevention & control
- Actinomycetales Infections / veterinary
- Animals
- Antibodies, Bacterial / blood
- Antibodies, Bacterial / immunology
- Enzyme-Linked Immunosorbent Assay / veterinary
- Horse Diseases / immunology
- Horse Diseases / prevention & control
- Horses
- Immunity, Maternally-Acquired
- Immunization, Passive / veterinary
- Pneumonia, Bacterial / immunology
- Pneumonia, Bacterial / prevention & control
- Pneumonia, Bacterial / veterinary
- Rhodococcus equi / immunology
- Rhodococcus equi / pathogenicity
Citations
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