Serum opsonization capacity, phagocytosis, and oxidative burst activity in neonatal foals in the intensive care unit.
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
The research article deals with the study of the reduced capacity for phagocytosis (a process where cells engulf and ingest harmful particles), oxidative burst activity (a rapid release of reactive oxygen species from cells), and serum opsonization (the process by which pathogens are marked for ingestion and elimination) in newborn foals in an intensive care unit compared to healthy, control foals.
Study Methodology
- The researchers collected blood samples from both hospitalized newborn foals and healthy, control foals for experimentation.
- The hospitalized foals were categorized as either sick or septic (a severe infection that spreads through the bloodstream) based on a sepsis score, and they were subjected to intravenous plasma transfusion.
- Phagocytosis, oxidative burst activity, and serum opsonization capacity were examined using flow cytometric analysis, a method that can analyze the physical and chemical characteristics of particles in a fluid as it passes through a laser.
- The amount of serum immunoglobulin (a type of antibody) and complement component 3 (a protein that plays a role in the immune response) was determined using radial immunodiffusion, a method to measure the concentration of proteins in a solution.
- The concentration of Serum amyloid A, a marker for inflammation in horses, was measured using a commercial solid-phase Sandwich ELISA Kit.
- All data collected from the experiment was analyzed using nonparametric and regression methods with an alpha value set at P = .05 (this means that a result is statistically significant if the p-value is less than or equal to 0.05.)
Research Findings
- Phagocytic functions of septic and sick foals were found to be lower than control foals in the beginning phase of the study.
- The serum opsonization capacity was significantly higher when bacteria were marked for elimination with serum from septic and sick foals than with serum from control foals on the first day of the study.
- The serum opsonization capacity for septic foals was similar to control foals on the second and fifth days of the study.
- The increase in serum opsonization capacity was not associated with an increase in serum complement C3 or immunoglobulin G concentrations independently.
Conclusions
The findings of this research suggest that the ability of cells to engulf and ingest harmful particles could be compromised in hospitalized foals. However, the results also suggest that the combined effect of opsonic elements provided by plasma transfusion may help to maintain the process by which pathogens are marked for ingestion and elimination during sepsis in these foals.
Cite This Article
Publication
Researcher Affiliations
- Department of Clinical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.
MeSH Terms
- Animals
- Animals, Newborn
- Complement C3 / metabolism
- Female
- Horse Diseases / blood
- Horse Diseases / metabolism
- Horses
- Immunoglobulins / blood
- Intensive Care Units
- Male
- Opsonin Proteins / blood
- Opsonin Proteins / metabolism
- Phagocytosis
- Respiratory Burst / physiology
- Sepsis / blood
- Sepsis / metabolism
- Serum Amyloid A Protein / metabolism
Citations
This article has been cited 1 times.- Long A, Nolen-Walston R. Equine Inflammatory Markers in the Twenty-First Century: A Focus on Serum Amyloid A.. Vet Clin North Am Equine Pract 2020 Apr;36(1):147-160.