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The Frequency of CD4+ T Cells in Women with Hashimoto's Thyroiditis
Masoume Nodehi1, Abolghasem Ajami2, Maryam Izad3,4
1Department of Applied Cell Sciences, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Insights
Hashimoto's thyroiditis patients show increased Th2 cells and interferon-gamma (IFN-γ) expression. Targeting these may help control disease progression in autoimmune thyroiditis.
Area of Science:
- Immunology
- Endocrinology
- Autoimmune Diseases
Background:
- Hashimoto's thyroiditis (HT) is the most common autoimmune disease with no definitive treatment.
- Understanding HT mechanisms is crucial for developing therapeutic strategies.
- This study investigates CD4+ T cell frequencies in HT patients compared to healthy individuals.
Purpose of the Study:
- To evaluate the frequency of specific CD4+ T cell subsets in patients with Hashimoto's thyroiditis.
- To compare these frequencies with those in healthy controls.
- To identify potential therapeutic targets for HT.
Main Methods:
- Flow cytometry was used to analyze T helper (Th)1, Th2, Th17, T regulatory type 1 (Tr1), and CD4+IL-4+IL-17+ cells.
- Patients were categorized into two groups based on antibody levels (anti-TPO and anti-TG).
- Mean fluorescent intensity of related cytokines was also assessed.
Main Results:
- Increased frequency of Th2 cells was observed in HT groups compared to controls, with a significant difference in one group (P=0.022).
- Elevated CD4+IL-4+IL-17+ cells were found in one HT group (P=0.027).
- Significantly higher interferon-gamma (IFN-γ) expression was noted in both HT groups (P=0.001).
Conclusions:
- No significant differences in Th17, Tr1 cells, or IL-17/IL-10 levels suggest limited therapeutic potential for these targets.
- Increased Th2 cells and IFN-γ expression in HT indicate potential therapeutic avenues.
- Reducing Th2 cell frequency or IFN-γ expression may be beneficial for managing HT progression.
Background:
Hashimoto's thyroiditis (HT) is the most prevalent autoimmune disease, and there is no definitive treatment available for this disease. To find the appropriate therapeutic approach, it is necessary to determine the mechanism of this disease. To achieve this purpose, the frequency of CD4+ T cells was evaluated in patients with HT and compared with healthy individuals.
Methods:
Twenty-six female patients with HT, aged 20 - 45 years, enrolled in this study. Based on the level of thyroglobulin antibody (anti-TG) and anti-thyroid peroxidase antibody (anti-TPO) in serum of patients with HT, they were divided into two groups. The serum level of anti-TPO was above 100 IU/mL in the group 1 (n = 13), whereas the serum levels of both anti-TPO and anti-TG were above 100 IU/mL in the group 2 (n = 13). Eleven healthy women were considered control group, or group 3. Using flow cytometry, the frequency of T helper (Th)1, Th2, Th17, T regulatory type 1 (Tr1), and LT CD4+IL-4+IL-17+ cells and mean fluorescent intensity (MFI) of their related cytokines were evaluated.
Results:
The frequency of Th2 cells in the groups 1 (anti-TPO > 100) and 2 (anti-TPO > 100 and anti-TG > 100) were more than control group. Only the difference between groups 3 (healthy control) and 2 was significant (P = 0.022). The frequency of LT CD4+IL-4+IL-17+ cells in the group 1 was significantly more than group 3 (P = 0.027); However, the difference between group 2 and 3 was not significant (P = 0.126). The expression of interferon-gamma (IFN-γ) in the group 2 (P = 0.001) and group 1 (P = 0.001) was significantly higher than group 3. The frequency of Th17, Th1, and Tr1 cells and MFI of IL-17 and IL-10 were not significantly different between the study groups.
Conclusions:
In the present study, no significant differences were observed in the frequency of Th17 and Tr1 cells and in MFI of IL-17 and IL-10 in comparison to healthy individuals. Therefore, trying to make a change in the population of these cells probably does not have a significant therapeutic effect. Since Th2 cells and the expression of IFN-γ increased in women with HT, reducing the frequency of Th2 cells or the expression of IFN-γ may be effective in controlling the disease progression. It may be helpful for these patients to prevent the progression of the disease.
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