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Intrarenal Injection of Escherichia coli in a Rat Model of Pyelonephritis
Published on: July 18, 2017
[The clinical significance of immunological indices in chronic pyelonephritis]
Insights
Pyelonephritis involves immune system changes, with reduced T-lymphocytes and altered immunoglobulin levels. This suggests a genetic predisposition to infection-mediated inflammation, impacting local immunity and receptor density.
Area of Science:
- Immunology
- Nephrology
- Microbiology
Background:
- Pyelonephritis is a complex kidney infection.
- Understanding its immunological underpinnings is crucial for effective management.
Purpose of the Study:
- To evaluate humoral and cellular immunity in patients with pyelonephritis.
- To investigate the role of immune system alterations in disease pathogenesis.
Main Methods:
- Assessed humoral immunity via immunoglobulin levels (IgA, IgM).
- Evaluated cellular immunity using lymphocyte rosette-test and T-lymphocyte subpopulation counts.
- Analyzed biopsy tissue for bacterial contamination and complement C3 levels.
Main Results:
- Significant decrease in T-lymphocytes (total, active, suppressors) observed during remission and exacerbation.
- IgA levels increased during remission, while IgM decreased, with further changes during aggravation.
- Complement C3 levels were comparable to controls; no biopsy contamination found.
Conclusions:
- Pyelonephritis exhibits significant cellular immunity suppression, particularly involving T-suppressors.
- Findings support the concept of pyelonephritis as a genetically determined, infection-mediated inflammatory disease.
- Local immune defects and altered receptor density, potentially triggered by urodynamic disorders, are characteristic.
Abstract:
Humoral and cellular immunity and data on biopsy tissue inoculation were evaluated for 72 patients with morphologically confirmed pyelonephritis. Cellular immunity was judged by lymphocyte rosette-test. T-lymphocyte subpopulation was counted in absolute numbers. No case of the biopsy bacterial contamination was shown bacteriologically. A complement C3 component was obtained in amounts similar to those in the controls. In remission IgA tended to a significant increase which (in IgM fall) continues in the disease aggravation. T-lymphocytes (total, active and suppressors) reduced in number, the changes arising in the remission with further intensification in a pyelonephritis exacerbation. Basing on the evidence obtained it is inferred that a significant suppression of cellular immunity, particularly T-suppressors, agrees with the idea of pyelonephritis as genetically determined, infection-mediated immune inflammation initially involving the medullary layer and urinary mucosa. The disease is characterized by defects in local immunity and changes in the density of receptors to the agent antigens. The predisposition came to action in disorders of urodynamics consequent to obstruction or ureteral hypotonicity of nonobstructive nature.
Related Concept Videos
Urinary Tract Infection II: Pathophysiology
Urinary Tract Infection III: Diagnostic Studies and Interprofessional Care
Acute Pyelonephritis I: Introduction
Acute Pyelonephritis II: Diagnostic Studies and Management
Acute Kidney Injury IV: Diagnostic Studies and Prevention
Urine Studies II: Urine Culture and Sensitivity Test
