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Role of interleukin-22 in tuberculosis patients
Shruti Gupta1, Mithu Banerjee1, Kavya Gauba1
1Department of Biochemistry, All India Institute of Medical Sciences, Jodhpur, India.
Journal of Basic and Clinical Physiology and Pharmacology
|October 14, 2022
Summary
Tuberculosis patients show decreased serum Interleukin-22 (IL-22) levels, yet its gene expression is significantly upregulated. This suggests IL-22 plays a complex role in modulating tissues during TB infection.
Area of Science:
- Immunology
- Infectious Diseases
- Molecular Biology
Background:
- Tuberculosis (TB) progression hinges on the interplay between microbial virulence and host immune responses, particularly T cell-mediated immunity.
- Interleukin-22 (IL-22) is implicated in host defense against microbial diseases, aiding cell proliferation and regeneration.
- The specific role of IL-22 in TB pathogenesis remains debated, despite its presence in granulomas.
Purpose of the Study:
- To investigate and compare serum levels and gene expression of IL-22 in TB patients versus healthy controls.
- To clarify the contradictory findings on IL-22's role in tuberculosis.
Main Methods:
- Serum IL-22 levels were quantified using enzyme-linked immunosorbent assay (ELISA).
- IL-22 gene expression was assessed via SYBR green-based quantitative PCR.
- The study included 87 TB patients and 85 healthy subjects.
Main Results:
- Serum IL-22 levels were significantly lower in TB patients (median 18.55 pg/mL) compared to controls (median 49.38 pg/mL).
- Conversely, IL-22 gene expression was significantly upregulated in TB patients (fold change 29.44).
Conclusions:
- A significant decrease in serum IL-22 contrasts with its upregulated gene expression in TB patients.
- IL-22 appears to play a critical role in tissue modulation during tuberculosis infection.
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