Expression Profile of NLRP3 Inflammasome in Peripheral Blood Mononuclear Cells and Plasma Interleukin-22 Level in Multiple Sclerosis | ||||
Egyptian Journal of Medical Microbiology | ||||
Article 33, Volume 34, Issue 2, April 2025, Page 277-284 PDF (532.65 K) | ||||
Document Type: New and original researches in the field of Microbiology. | ||||
DOI: 10.21608/ejmm.2025.352611.1441 | ||||
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Authors | ||||
Heba M. Elbatal ![]() ![]() | ||||
1Medical Microbiology and Immunology Department, Faculty of Medicine, Cairo University | ||||
2Neurology Department, Faculty of Medicine, Cairo University | ||||
Abstract | ||||
Background: Multiple sclerosis (MS) is a long-lasting neurodegenerative disorder that primarily impacts young adults. Interleukin-22 (IL-22) and the nucleotide-binding oligomerization domain-like receptor protein 3 (NLRP3) inflammasome play critical roles in host innate immunity and have been linked to several autoimmune diseases. Objectives: The objectives of our work are to assess the plasma levels of IL-22 and the expression of the NLRP3 inflammasome in peripheral blood mononuclear cells (PBMCs) in MS patients versus healthy controls. Furthermore, to correlate the level of plasma IL-22 and NLRP3 inflammasome expression in MS patients. Methodology: The study examined 40 patients with MS and 40 matched healthy controls. It measured plasma IL-22 using enzyme-linked immunosorbent assay (ELISA) and assessed NLRP3 expression through real-time reverse transcription polymerase chain reaction (RT-PCR). Results: Patients with MS exhibited markedly elevated levels of plasma IL-22 (P < 0.0001) and a significantly elevated relative expression of NLRP3 (P < 0.0001). Additionally, a significant positive correlation was observed between plasma IL-22 and NLRP3 relative expression (r = 0.45, P = 0.003). Also, ssignificant positive correlations were noted between plasma IL-22 level and both the Expanded Disability Status Scale (EDSS) and frequency of relapses in the past year (r = 0.49, 0.55, P-values = 0.001, 0.0002 respectively). Similarly, EDSS and frequency of relapses in the past year were positively correlated with NLRP3 relative expression (r = 0.4, 0.69, P-values = 0.01, < 0.00001 respectively). Conclusion: Both IL-22 and NLRP3 inflammasome could be encouraging prognostic markers and potential therapeutic targets for MS. | ||||
Keywords | ||||
EDSS; Interleukin-22; Multiple sclerosis; NLRP3; inflammasome | ||||
Supplementary Files
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