Mirghanizadeh Bafghi Seyyed AmirHossein, Fesahat Farzaneh, Zare Fateme, Imani Maryam, Vahidi Serajoddin, Ansariniya Hossein, ZareHoroki Ali, Hadinedoushan Hossein
Reproductive Immunology Research Center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Research and Clinical Center for Infertility, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Front Immunol. 2024 Dec 6;15:1507885. doi: 10.3389/fimmu.2024.1507885. eCollection 2024.
To address knowledge gaps, this study aimed to investigate the involvement of inflammasomes in the etiology of azoospermia. This study focused on the gene expression of key inflammasome components, including , and .
We analyzed gene expression in blood and testicular tissue from patients with obstructive azoospermia (OA) and non-obstructive azoospermia (NOA). Additionally, we compared IL-1β and IL-18 expression levels in seminal plasma samples using the Enzyme-Linked Immunosorbent Assay (ELISA) method. For comparison, blood samples from normospermic (NS) individuals were also genetically evaluated.
Our results indicated significantly higher gene expression of inflammasome components in NOA patients than those in OA patients either in blood or in testicular tissue. Both azoospermic groups exhibited higher mRNA levels of inflammasome genes comparing with those from blood samples of NS men. Seminal plasma samples showed significantly increased levels of IL-1β and IL-18 in NOA patients compared to men with OA. The ROC curve analysis indicated strong and significant predictive power of and gene expression profiles between NOA vs. NS patients and NOA vs. OA.
Our findings highlight the role of hidden chronic inflammation in azoospermia, particularly within the NOA group. This study provides a foundation for further detailed research, which could aid in the development of diagnostic panels to differentiate between various azoospermic groups.
为填补知识空白,本研究旨在调查炎性小体在无精子症病因中的作用。本研究聚焦于关键炎性小体成分的基因表达,包括 、 和 。
我们分析了梗阻性无精子症(OA)和非梗阻性无精子症(NOA)患者血液和睾丸组织中的基因表达。此外,我们使用酶联免疫吸附测定(ELISA)方法比较了精液样本中白细胞介素-1β(IL-1β)和白细胞介素-18(IL-18)的表达水平。作为对照,还对正常精子症(NS)个体的血液样本进行了基因评估。
我们的结果表明,无论是在血液还是睾丸组织中,NOA患者炎性小体成分的基因表达均显著高于OA患者。与NS男性血液样本相比,两个无精子症组炎性小体基因的mRNA水平均较高。与OA男性相比,NOA患者的精液样本中IL-1β和IL-18水平显著升高。受试者工作特征(ROC)曲线分析表明, 和 基因表达谱在NOA与NS患者以及NOA与OA之间具有强大且显著的预测能力。
我们的研究结果突出了隐匿性慢性炎症在无精子症中的作用,尤其是在NOA组中。本研究为进一步的详细研究奠定了基础,这可能有助于开发诊断面板以区分不同的无精子症组。