Chun Kyeunghwa, Na Yujeong, Kim Byeongyong, Lee Dongjin, Choi Jongseo, Kim Gwanyoung, Kim Sokho, Kim Min-Soo
Daewoong Pharmaceutical Co., Ltd., 72, Dugye-ro, Pogok-eup, Cheoin-gu, Yongin-si 17028, Gyeonggi-do, Republic of Korea.
College of Pharmacy, Pusan National University, 2, Busandaehak-ro 63beon-gil, Geumjeong-gu, Busan 46241, Republic of Korea.
Viruses. 2025 Feb 21;17(3):301. doi: 10.3390/v17030301.
Influenza A virus (IAV) is a major cause of respiratory infections worldwide. Current preventive measures, though effective for decades, face limitations due to the continuous evolution of viral strains and challenges in targeting specific viral proteins. In this study, we conducted in vivo screenings to evaluate the antiviral properties of various promising polymers to overcome the limitations of current virus infection prevention strategies. Subsequently, we performed detailed physiological and pathological assessments over an extended infection period. In the animal experiments regarding weight loss, a key symptom of viral infection, the group treated with xanthan gum (XG) showed significant suppression of weight loss compared to the untreated group starting from 3 DPI. Throughout the experiment, the treated group maintained a body weight similar to that of the uninfected group. In the virus titration and lung tissue pathology analysis, the group treated with the test substance showed a significantly lower viral load and tissue pathology results closer to normal compared to the untreated group. Additionally, we conducted in vitro combination treatment experiments to evaluate the antiviral ability of XG in conjunction with camostat, a previously known TMPRSS2 inhibitor. The results demonstrated that in the combination-treated groups, XG and camostat exhibited significantly higher cell viability at lower concentrations compared to the single-treatment groups for influenza A H1N1, A H3N2, and B type. These results indicate that XG possesses potential capabilities in inhibiting respiratory viruses and may be utilized in conjunction with existing antiviral treatments.
甲型流感病毒(IAV)是全球范围内呼吸道感染的主要病因。当前的预防措施虽然几十年来一直有效,但由于病毒株的不断进化以及靶向特定病毒蛋白方面的挑战而面临局限。在本研究中,我们进行了体内筛选,以评估各种有前景的聚合物的抗病毒特性,以克服当前病毒感染预防策略的局限性。随后,我们在延长的感染期内进行了详细的生理和病理评估。在关于体重减轻(病毒感染的一个关键症状)的动物实验中,从感染后第3天起,与未治疗组相比,用黄原胶(XG)治疗的组体重减轻得到了显著抑制。在整个实验过程中,治疗组的体重维持在与未感染组相似的水平。在病毒滴定和肺组织病理学分析中,与未治疗组相比,用受试物质治疗的组病毒载量显著更低,组织病理学结果更接近正常。此外,我们进行了体外联合治疗实验,以评估XG与之前已知的TMPRSS2抑制剂卡莫司他联合使用时的抗病毒能力。结果表明,在联合治疗组中,与甲型H1N1、H3N2流感病毒和乙型流感病毒的单药治疗组相比,XG和卡莫司他在较低浓度下表现出显著更高的细胞活力。这些结果表明,XG具有抑制呼吸道病毒的潜在能力,并且可以与现有的抗病毒治疗联合使用。