[Changes of FoxP3, CD4(+)CD25(+) regulatory T cells, TLR2 and TLR9 in children with infectious mononucleosis]
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Updated: May 11, 2026

Separation of Immune Cell Subpopulations in Peripheral Blood Samples from Children with Infectious Mononucleosis
Published on: September 7, 2022
Qiang Wang1, Zuo-Feng Wang, Mei Cao
1Department of Pediatrics, Sichuan Province People's Hospital, Sichuan Province, China. wangchunwei_4@hotmail.com
Insights
Infectious mononucleosis (IM) patients in the acute stage show reduced regulatory T cells (Treg) and FoxP3, but increased TLR2 and TLR9 expression. These levels normalize during recovery, suggesting a role in IM pathogenesis.
Area of Science:
- Immunology
- Molecular Biology
Context:
- Infectious mononucleosis (IM) is a common viral illness.
- Understanding the immune response in IM is crucial for managing the disease.
Purpose:
- To investigate the role of Toll-like receptors (TLR2, TLR9), regulatory T cells (CD4(+)CD25(+)), and the transcription factor FoxP3 in the pathogenesis of infectious mononucleosis (IM) in children.
Summary:
- Acute IM patients exhibited significantly higher TLR2 and TLR9 mRNA levels compared to healthy controls and recovered patients.
- Conversely, CD4(+)CD25(+) regulatory T cells and FoxP3 mRNA levels were significantly lower in acute IM patients than in controls.
- These immune markers normalized in the recovery stage, indicating their dynamic changes during the disease course.
Impact:
- The findings suggest that TLR2 and TLR9 upregulation, alongside Treg and FoxP3 downregulation, contribute to IM pathogenesis.
- This research provides insights into the immune mechanisms underlying IM and potential therapeutic targets.
Abstract:
The aim of this study was to investigate the effects of TLR2, TLR9, CD4(+)CD25(+) regulatory T cells (Treg) and transcription factor FoxP3 in the pathogenesis of children with infectious mononucleosis (IM). Thirty-five acute IM patients admitted in our hospital from April 2010 to January 2011 were enrolled in this study. Thirty-five healthy subjects were taken as control. The thirty-five patients before treatment were considered as patients in acute stage, after treatment and without clinical symptom they were thought as patients in recovery stage. The expression levels of TLR2, TLR9 and FoxP3 mRNA were detected by real time PCR using SYBR Green I. The expression of T lymphocyte subset CD4(+)CD25(+) in peripheral blood mononuclear cells was detected by flow cytometry. The results showed that the relative levels of TLR2 mRNA (4.03 ± 0.56), TLR9 mRNA (8.88 ± 1.56) in peripheral blood mononuclear cells of IM patients in acute stage were significantly higher than those of the controls [TLR2 mRNA (2.22 ± 0.57), TLR9 mRNA (3.63 ± 1.30)] and IM patients in recovery stage [TLR2 mRNA (2.76 ± 0.83), TLR9 mRNA (5.34 ± 1.60)] (P < 0.01). The result of CD4(+)CD25(+) (2.38 ± 1.32%) and relative level of FoxP3 mRNA(2.82 ± 0.90) in peripheral blood mononuclear cells of IM patients in acute stage were lower than those of the control [CD4(+)CD25(+) (7.85 ± 1.97%), FoxP3 mRNA (4.65 ± 1.23) ] (P < 0.01). There was no significant difference in CD4(+)CD25(+) (6.81 ± 1.84%), FoxP3 mRNA(4.11 ± 1.37) levels between IM patients in recovery stage and the controls (P > 0.05). It is concluded that the expression of CD4(+)CD25(+)regulatory T cells is reduced, and its special transcription factor FoxP3 mRNA is down-regulated, but expression levels of TLR2 mRNA, TLR9 mRNA are up-regulated in IM patients of acute stage.
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