School of Pharmaceutical Sciences, Siksha "O" Anusandhan, Odisha, India.
Institute of Dental Sciences, Siksha "O" Anusandhan University, Odisha, India.
Arch Med Res. 2022 Feb;53(2):122-130. doi: 10.1016/j.arcmed.2021.09.008. Epub 2021 Oct 22.
Over the period, viral infections remain the utmost challenge in front of the scientific community. Continuous shifting and drafting of viral antigenic peptides are the main drivers in the development of antiviral drug resistance. The resurgence of disease, difficulties facing the development of an effective vaccine and undesirable immunological outcomes, foster to develop an alternative therapeutic approach to combat viral infections. Biomimetic nature of viral particles competent to invade the host cell by downregulating the expression of immune responsive cells. To revive from such complications, strengthening the innate immunity places first and foremost defense mechanisms to restrict viral infiltration. Variegated probiotic strains show antiviral activity by stimulating the macrophage and dendritic cell to secret the inflammation response mediated chemokines and cytokines, production of antimicrobial peptides, and biosurfactants, modulate the antiviral gens expression, alter the proportional functionality of CD4CD25Foxp3 regulatory cells (Tregs), etc. With the appreciation for the antiviral activity and health benefits, however, the selectivity of specific probiotic strain from the diversified microbiome, the interactive molecular mechanism of probiotics, viability and sustainability of a specific number of a probiotic strain at the end of the shelf life, stability, selection of the formulation materials, identification and validation of the key process parameters have the major challenges for the development of an effective probiotic therapy against viral infections.
在这段时间里,病毒感染仍然是科学界面临的最大挑战。病毒抗原肽的持续转移和起草是抗病毒药物耐药性发展的主要驱动因素。疾病的复发、有效疫苗开发面临的困难和不理想的免疫结果,促使人们开发一种替代的治疗方法来对抗病毒感染。病毒颗粒的仿生特性能够通过下调免疫反应细胞的表达来入侵宿主细胞。为了从这些并发症中恢复过来,增强先天免疫是限制病毒渗透的首要防御机制。各种益生菌菌株通过刺激巨噬细胞和树突状细胞分泌炎症反应介导的趋化因子和细胞因子、产生抗菌肽和生物表面活性剂、调节抗病毒基因表达、改变 CD4CD25Foxp3 调节性细胞 (Tregs) 的比例功能等方式发挥抗病毒活性。然而,随着对抗病毒活性和健康益处的认识,从多样化的微生物组中选择特定的益生菌菌株、益生菌的相互作用分子机制、益生菌在货架寿命结束时的特定数量的生存能力和可持续性、稳定性、配方材料的选择、关键过程参数的识别和验证,这些都对开发针对病毒感染的有效益生菌疗法构成了重大挑战。