HLA‐DR+ CD45RAˉ Tregs and CD28ˉ Treg‐like cells: Potential immunologic biomarkers for reproductive aging

CD28 窦卵泡 免疫学 医学 调节性T细胞 人类白细胞抗原 生物 激素 内科学 免疫系统 T细胞 白细胞介素2受体 抗原
作者
Kahindo P. Muyayalo,Song Su,Chunyan Liu,Guang‐Shun Gong,Yu‐Jing Zhang,Hui Zhou,Li Shen,Aihua Liao
出处
期刊:American Journal of Reproductive Immunology [Wiley]
卷期号:89 (6) 被引量:4
标识
DOI:10.1111/aji.13591
摘要

Abstract Problem This study aimed to identify subsets of regulatory T cells (Tregs) associated with ovarian aging and determine whether they can be used as markers of reproductive aging. Method This prospective cohort study was conducted among women of reproductive age. Basic physiological characteristics, reproductive hormones, Treg cell subsets, and correlations between these parameters were assessed. The POSEIDON criteria was used to identify women with low reproductive potential. Results The percentages of HLA‐DR + CD45RAˉ Tregs and CD28ˉ Treg‐like cells significantly increased with age. Women between 40 and 49 years had significantly higher percentages of HLA‐DR + CD45RAˉ Tregs and CD28ˉ Treg‐like cells than those at 20–29, 30–34, and 35–39 years old. Age positively correlated with FSH levels and the percentages of HLA‐DR + CD45RAˉ Tregs and CD28ˉ Treg‐like cells, but inversely correlated with antral follicle count (AFC) and AMH levels. Interestingly, a positive correlation was found between the percentages of HLA‐DR + CD45RAˉ Tregs and FSH levels, whereas an inverse correlation was found between those of HLA‐DR + CD45RAˉ Tregs and AFC or AMH levels. Furthermore, a significant positive correlation was observed between the percentages of CD28ˉ Treg‐like cells and AFC. Based on POSEIDON criteria, women with the percentages of HLA‐DR + CD45RAˉ Tregs and CD28ˉ Treg‐like cells above reference value ranges were assigned to the low prognosis groups. Conclusion These findings suggest that HLA‐DR + CD45RAˉ Tregs and CD28ˉ Treg‐like cells can be used as immunologic markers of reproductive aging, which helps clinicians identify women with low reproductive potential and establish individualized therapeutic strategies.
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