Sun Der-Shan, Lien Te-Sheng, Chang Hsin-Hou
Department of Molecular Biology and Human Genetics, Tzu-Chi University, Hualien 970, Taiwan.
Int J Mol Sci. 2025 Feb 22;26(5):1898. doi: 10.3390/ijms26051898.
Virus-induced antibodies represent a dual-edged sword in the immune response to viral infections. While antibodies are critical for neutralizing pathogens, some can paradoxically exacerbate disease severity through mechanisms such as antibody-dependent enhancement (ADE), autoantibody, and prolonged inflammation. Long coronavirus disease (COVID) and dengue hemorrhagic fever (DHF) exemplify conditions where pathogenic antibodies play a pivotal role in disease progression. Long COVID is associated with persistent immune dysregulation and autoantibody production, leading to chronic symptoms and tissue damage. In DHF, pre-existing antibodies against dengue virus contribute to ADE, amplifying viral replication, immune activation, and vascular permeability. This review explores the mechanisms underlying these pathogenic antibody responses, highlighting the shared pathways of immune dysregulation and comparing the distinct features of both conditions. By examining these studies, we identify key lessons for therapeutic strategies, vaccine design, and future research aimed at mitigating the severe outcomes of viral infections.
病毒诱导产生的抗体在针对病毒感染的免疫反应中是一把双刃剑。虽然抗体对于中和病原体至关重要,但有些抗体却可能通过抗体依赖增强作用(ADE)、自身抗体和持续性炎症等机制反常地加剧疾病严重程度。长新冠和登革出血热就是致病性抗体在疾病进展中起关键作用的例证。长新冠与持续性免疫失调和自身抗体产生有关,会导致慢性症状和组织损伤。在登革出血热中,先前存在的抗登革病毒抗体促成了ADE,放大了病毒复制、免疫激活和血管通透性。本综述探讨了这些致病性抗体反应背后的机制,突出了免疫失调的共同途径,并比较了这两种病症的不同特征。通过审视这些研究,我们确定了针对治疗策略、疫苗设计以及旨在减轻病毒感染严重后果的未来研究的关键经验教训。