Doghish Ahmed S, Abulsoud Ahmed I, Nassar Yara A, Nasr Sami Mohamed, Mohammed Osama A, Abdel-Reheim Mustafa Ahmed, Rizk Nehal I, Lutfy Radwa H, Abdel Mageed Sherif S, Ismail Menattallah A, Abd-Elhalim Haytham M, Awad Farah A, Fayez Salma Zaki, Elimam Hanan, Mansour Reda M
Department of Biochemistry, Badr University in Cairo (BUC), Badr City, Cairo, Egypt.
Biochemistry and Molecular Biology Department, Faculty of Pharmacy (Boys), Al-Azhar University, Nasr City, Cairo, Egypt.
J Biochem Mol Toxicol. 2025 Jan;39(1):e70119. doi: 10.1002/jbt.70119.
Mycobacterium tuberculosis (Mtb) complex, responsible for tuberculosis (TB) infection, continues to be a predominant global cause of mortality due to intricate host-pathogen interactions that affect disease progression. MicroRNAs (miRNAs), essential posttranscriptional regulators, have become pivotal modulators of these relationships. Recent findings indicate that miRNAs actively regulate immunological responses to Mtb complex by modulating autophagy, apoptosis, and immune cell activities. This has resulted in increased interest in miRNAs as prospective diagnostic indicators for TB, especially in differentiating active infection from latent or inactive stages. Variations in miRNA expression during Mtb infection indicate disease progression and offer insights into the immune response. Furthermore, miRNAs present potential as therapeutic targets in host-directed therapy (HDT) techniques for TB infection. This work examines the function of miRNAs in TB pathogenesis, with the objective of identifying particular miRNAs that regulate the immune response to the Mtb complex, evaluating their diagnostic value and exploring their therapeutic implications in host-directed therapy for TB infection. The objective is to enhance comprehension of how miRNAs can facilitate improved diagnosis and treatment of TB.
结核分枝杆菌(Mtb)复合体是导致结核病(TB)感染的病原体,由于其与宿主之间复杂的相互作用影响疾病进展,它仍是全球主要的致死原因。微小RNA(miRNA)作为关键的转录后调节因子,已成为这些相互关系的关键调节因子。最近的研究结果表明,miRNA通过调节自噬、凋亡和免疫细胞活性,积极调控对Mtb复合体的免疫反应。这使得人们对miRNA作为结核病潜在诊断指标的兴趣日益增加,尤其是在区分活动性感染与潜伏或非活动阶段方面。Mtb感染期间miRNA表达的变化表明疾病的进展,并为免疫反应提供了见解。此外,miRNA在针对结核病感染的宿主导向疗法(HDT)技术中具有作为治疗靶点的潜力。这项工作研究了miRNA在结核病发病机制中的作用,目的是识别调节对Mtb复合体免疫反应的特定miRNA,评估它们的诊断价值,并探索它们在针对结核病感染的宿主导向疗法中的治疗意义。目的是加深对miRNA如何促进结核病诊断和治疗改善的理解。