The First Affiliated Hospital of Xinjiang Medical University, Medical Testing Center, Xinjiang, China; State Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia, Clinical Laboratory Center, Tumor Hospital Affiliated to Xinjiang Medical University, Urumqi, Xinjiang 830011, PR China.
State Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia, Clinical Laboratory Center, Tumor Hospital Affiliated to Xinjiang Medical University, Urumqi, Xinjiang 830011, PR China.
Exp Parasitol. 2023 Nov;254:108623. doi: 10.1016/j.exppara.2023.108623. Epub 2023 Oct 2.
One of the primary reasons for the successful patriotization of Echinococcus multilocularis in patients is its ability to induce host immune tolerance. This study examined the expression of the immunosuppressive Tim-3/Galectin-9 pathway, CD8+T cells, and related factors in AE patients. The aim was to analyze the relationship between the Tim-3/Galectin-9 pathway and CD8+T cells in this disease and further understand the mechanism of immune tolerance induced by cystic echinococcosis.
Using flow cytometry, we evaluated the expression of CTL, CD8CD28-T cells, CD8CD28 + IFN-γ + T cells, CD8CD28+perforin + T cells, CD8CD28+granzyme B + T cells, CD8CD28-IL-10 + T cells, CD8CD28-TGF-β+T cells, and Tim-3 expression on CD8+T cells in the peripheral blood of control (n = 30) and AE patients (n = 33). qRT-PCR was used to measure CD107a and Tim-3/Galectin-9 mRNA levels in PBMCs from the control and AE groups. Immunohistochemistry was employed to detect IL-10, TGF-β, and Tim-3/Galectin-9 expressions in the infected livers of AE patients.
AE patients exhibited a significant decrease in peripheral blood CTL ratio (P < 0.001) and an increase in CD8CD28+IFN-γ+T cell ratio (P < 0.001). No significant changes were observed in the ratios of CD8CD28+perforin + T cells (P = 0.720) and CD8CD28+granzyme B + T cells (P = 0.051). The proportions of CD8CD28-T cells (P < 0.001), CD8CD28-IL-10 + T cells (P < 0.001), and CD8CD28-TGF-β+T cells (P < 0.001) were notably higher than in the control group. The expression of Tim-3 on CTL and CD8CD28-T cells in AE patients was significantly upregulated (P < 0.001, P < 0.001). AE patients displayed a substantial decrease in peripheral blood PBMC CD107a mRNA levels (P < 0.001) and significant elevations in Tim-3/Galectin-9 mRNA levels (P < 0.001, P < 0.001). A negative correlation was observed between CD107a mRNA levels and both Tim-3 (r^2 = 0.411, P < 0.001) and Galectin-9 (r = 0.180, P = 0.019) mRNA levels. Expressions of IL-10 (P < 0.001), TGF-β (P < 0.001), and Tim-3/Galectin-9 (P < 0.001, P < 0.001) in AE patient-infected livers were significantly higher than in uninfected regions. IL-10 and TGF-β expressions showed a positive correlation with Tim-3/Galectin-9.
This study suggests that the high expression of Tim-3 on CD8+T cell surfaces in AE patients might promote an increase in CD8CD28-T cells and related factors, while suppressing CTL and related factor expressions. This potentially induces the onset of immune tolerance, which is unfavorable for the clearance of Echinococcus multilocularis in patients, leading to the exacerbation of persistent infections.
泡型包虫病(AE)患者异体抗原成功归巢的主要原因之一是其诱导宿主免疫耐受的能力。本研究检测了免疫抑制性 Tim-3/Galectin-9 通路、CD8+T 细胞及其相关因子在 AE 患者中的表达,旨在分析 Tim-3/Galectin-9 通路与 CD8+T 细胞在该疾病中的关系,并进一步了解包虫囊肿诱导免疫耐受的机制。
采用流式细胞术检测 AE 患者(n=33)和健康对照组(n=30)外周血中 CTL、CD8CD28-T 细胞、CD8CD28+IFN-γ+T 细胞、CD8CD28+perforin+T 细胞、CD8CD28+granzyme B+T 细胞、CD8CD28-IL-10+T 细胞、CD8CD28-TGF-β+T 细胞和 CD8+T 细胞表面 Tim-3 的表达。qRT-PCR 检测 PBMC 中 CD107a 和 Tim-3/Galectin-9mRNA 的水平。免疫组化检测 AE 患者感染肝组织中 IL-10、TGF-β和 Tim-3/Galectin-9 的表达。
AE 患者外周血 CTL 比例显著降低(P<0.001),CD8CD28+IFN-γ+T 细胞比例升高(P<0.001)。CD8CD28+perforin+T 细胞(P=0.720)和 CD8CD28+granzyme B+T 细胞(P=0.051)比例无显著变化。CD8CD28-T 细胞(P<0.001)、CD8CD28-IL-10+T 细胞(P<0.001)和 CD8CD28-TGF-β+T 细胞(P<0.001)比例明显高于对照组。AE 患者 CTL 和 CD8CD28-T 细胞表面 Tim-3 的表达显著上调(P<0.001,P<0.001)。AE 患者外周血 PBMC CD107a mRNA 水平显著降低(P<0.001),Tim-3/Galectin-9 mRNA 水平显著升高(P<0.001,P<0.001)。CD107a mRNA 水平与 Tim-3(r^2=0.411,P<0.001)和 Galectin-9(r=0.180,P=0.019)mRNA 水平呈负相关。AE 患者感染肝组织中 IL-10(P<0.001)、TGF-β(P<0.001)和 Tim-3/Galectin-9(P<0.001,P<0.001)的表达明显高于未感染区域。IL-10 和 TGF-β 的表达与 Tim-3/Galectin-9 呈正相关。
本研究表明,AE 患者 CD8+T 细胞表面高表达 Tim-3,可能促进 CD8CD28-T 细胞及其相关因子的增加,同时抑制 CTL 及其相关因子的表达,从而诱导免疫耐受的发生,不利于患者体内细粒棘球蚴的清除,导致持续性感染的加重。