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Separation of Immune Cell Subpopulations in Peripheral Blood Samples from Children with Infectious Mononucleosis
Published on: September 7, 2022
Manganese and the cGAS-STING Pathway in Infectious Mononucleosis Caused by Epstein-Barr Virus Infection
Jinjin Shi1,2, Yuqin Li1, Dandan Zhang1
1Department of Infectious Disease, Children's Hospital of Soochow University, Soochow University, Suzhou, China.
Abstract:
To study the clinical significance of manganese (Mn) in the serum of children with infectious mononucleosis (IM) caused by Epstein-Barr virus (EBV) infection, we analyzed the correlation between Mn and the cyclic GMP-AMP synthase (cGAS)-stimulator of interferon genes (STING) pathway and explored the immune pathogenesis of EBV infection. Children diagnosed with IM comprised the IM group, and healthy children during the same period were selected as the normal control group. Real-time reverse transcription-polymerase chain reaction was used to detect the mRNA expression levels of cGAS, STING, Tank-binding kinase 1 (TBK1), interferon regulatory factor 3 (IRF3), and related inflammatory factors, and Mn in serum was detected by inductively coupled plasma mass spectrometry. Interferon (IFN)-α and IFN-β expression levels in serum were detected by enzyme-linked immunosorbent assay, and the correlation between Mn levels and clinical manifestations and laboratory tests was analyzed. Mn levels and the expression levels of cGAS, STING, and related inflammatory factors were significantly higher in children with IM than in healthy children. Furthermore, Mn levels in children with IM were positively correlated with the expression levels of cGAS and related inflammatory factors. Thus, Mn, cGAS, STING, and inflammatory cytokines may be involved in the immune mechanism of IM caused by EBV infection.
Insights
Manganese (Mn) levels are elevated in children with infectious mononucleosis (IM) and correlate with the cGAS-STING pathway, suggesting a role in Epstein-Barr virus (EBV) immune pathogenesis.
Area of Science:
- Immunology
- Virology
- Pediatrics
- Environmental Health
Background:
- Infectious mononucleosis (IM) is a common viral illness caused by the Epstein-Barr virus (EBV).
- The innate immune response, involving the cyclic GMP-AMP synthase (cGAS)-stimulator of interferon genes (STING) pathway, is crucial in viral infections.
- Manganese (Mn) is an essential trace element with potential immunomodulatory roles.
Purpose of the Study:
- To investigate the clinical significance of serum manganese (Mn) levels in children with EBV-induced infectious mononucleosis (IM).
- To analyze the correlation between Mn levels and the cGAS-STING pathway in IM.
- To explore the immune pathogenesis of EBV infection involving Mn and the cGAS-STING pathway.
Main Methods:
- Serum Mn levels were quantified using inductively coupled plasma mass spectrometry.
- mRNA expression of cGAS, STING, TBK1, IRF3, and inflammatory factors was measured by real-time RT-PCR.
- Serum Interferon-alpha (IFN-α) and IFN-beta (IFN-β) levels were determined by ELISA.
Main Results:
- Children with IM exhibited significantly higher serum Mn levels compared to healthy controls.
- Elevated expression of cGAS, STING, and inflammatory factors was observed in children with IM.
- Serum Mn levels positively correlated with cGAS expression and inflammatory factor levels in IM patients.
Conclusions:
- Serum manganese may play a significant role in the immune response during EBV-induced infectious mononucleosis in children.
- The cGAS-STING pathway and associated inflammatory cytokines are implicated in the immune pathogenesis of IM.
- Mn, cGAS, STING, and inflammatory cytokines are potential contributors to the immune mechanisms underlying IM.

