梅毒发病机制:宿主免疫应答与病原体免疫逃避。

Andy Liu,Lorenzo Giacani,Iskra Tuero,Jeffrey D Klausner
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引用次数: 0

摘要

梅毒由苍白螺旋体亚种苍白螺旋体(梅毒螺旋体)引起,尽管可以预防和治愈,但仍然是一个重大的全球卫生问题。病原体利用基于毒力因子的策略和入侵免疫特权部位逃避免疫系统的能力使未经治疗的宿主持续感染。这篇最新的翻译描述了梅毒的宿主先天和适应性免疫反应,以及梅毒螺旋体避免免疫清除的复杂机制。免疫谱分析的最新进展增强了我们对宿主免疫反应的理解,并确定了疾病分期和治疗监测的潜在生物标志物。然而,关于苍白球绦虫的免疫逃避机制、细胞和体液免疫的动力学以及针对苍白球绦虫的长期保护性免疫反应的特征,知识差距仍然存在。通过整合微生物学、免疫学和多组学方法来弥合这些差距,对于推进诊断工具、治疗策略和疫苗开发以最终减轻梅毒的全球负担至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Syphilis Pathogenesis: Host Immune Response versus Pathogen Immune Evasion.
Syphilis, caused by Treponema pallidum subspecies pallidum (T. pallidum), remains a significant global health problem despite being preventable and curable. The pathogen's ability to evade the immune system using virulence factor-based strategies and by invading immune-privileged sites enables persistent infection in the untreated host. This translational update describes the host innate and adaptive immune responses in syphilis and the sophisticated mechanisms employed by T. pallidum to avoid immune clearance. Recent advances in immune profiling have enhanced our understanding of the host immune response and identified potential biomarkers for disease staging and treatment monitoring. However, knowledge gaps remain regarding T. pallidum's immune evasion mechanisms, the dynamics of cellular and humoral immunity, and the characteristics of long-term protective immune responses against T. pallidum. Bridging these gaps by integrating microbiology, immunology, and multiomics approaches is crucial for advancing diagnostic tools, therapeutic strategies, and vaccine development to ultimately reduce the global burden of syphilis.
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