Jabeen Kehkshan, Javed Aneela, Waris Asim, Shahzad Shaheen
Genomics Research Lab, Department of Biological Sciences, International Islamic University Islamabad, Islamabad, Pakistan.
Healthcare Biotechnology, Atta-ur Rahman School of Applied Biosciences (ASAB), National University of Sciences and Technology (NUST), H-12 Campus, Islamabad, Pakistan.
Iran J Basic Med Sci. 2023 Feb;26(2):176-182. doi: 10.22038/IJBMS.2022.65983.14536.
Hepatitis B virus (HBV) infection alters the cytokines production to establish persistent infection. A reversion of cytokines back to their normal state can be a promising therapeutic approach to establish an optimal host immune response.
We investigated the alteration in expression of IL-15 and IL-11 after HBV infection and in PBMCs of 63 individuals divided into various HBV-infected patient groups. The mRNA expression was evaluated post-anti-oxidant and calcium modulators treatment by Real-time qPCR.
mRNA expression of both cytokines, post-infection was down-regulated considerably. Interestingly, in line with results, both cytokines' expression was intensively down-regulated in chronic HBV-infected individuals rather than healthy controls. Both cytokines' expression was up-regulated in cases of recovery compared with the inactive carriers and chronic HBV-infected individuals. IL-15 mRNA expression was significantly up-regulated in both cell lines post EGTA and Ru360 treatment while a significant increase was observed in the HepAD38 cell line with NAC and BAPTA treatment. IL-11 mRNA expression was significantly up-regulated in the HepG2 cell line after all modulator treatments, whereas in the HepAd38 cell line it was observed after BAPTA treatment. Our results thus indicate that viral infection tends to down-regulate the expression of cytokines and an up-regulation is an indication of recovery.
Treatment of anti-oxidants and calcium modulators has resulted in the successful restoration of these cytokines thus pointing towards the use of calcium modulators to boost natural antiviral cytokine production.
乙型肝炎病毒(HBV)感染会改变细胞因子的产生以建立持续感染。将细胞因子恢复到正常状态可能是建立最佳宿主免疫反应的一种有前景的治疗方法。
我们调查了63名分为不同HBV感染患者组的个体在HBV感染后外周血单个核细胞(PBMC)中白细胞介素-15(IL-15)和白细胞介素-11(IL-11)表达的变化。通过实时定量聚合酶链反应(Real-time qPCR)评估抗氧化剂和钙调节剂处理后的mRNA表达。
感染后两种细胞因子的mRNA表达均显著下调。有趣的是,与结果一致,在慢性HBV感染个体而非健康对照中,两种细胞因子的表达均被强烈下调。与非活动性携带者和慢性HBV感染个体相比,恢复病例中两种细胞因子的表达均上调。在EGTA和Ru360处理后,两种细胞系中IL-15 mRNA表达均显著上调,而在NAC和BAPTA处理的HepAD38细胞系中观察到显著增加。在所有调节剂处理后,HepG2细胞系中IL-11 mRNA表达显著上调,而在HepAd38细胞系中,在BAPTA处理后观察到上调。因此,我们的结果表明病毒感染倾向于下调细胞因子的表达,而上调则表明恢复。
抗氧化剂和钙调节剂的治疗成功恢复了这些细胞因子的表达,从而表明使用钙调节剂来促进天然抗病毒细胞因子的产生。