感染中黏附相关发病机制的进展。
Advances in adhesion-related pathogenesis in infection.
作者信息
Sun Bingyue, Ling Yaozheng, Li Junhui, Ma Li, Jie Zige, Luo Hongbing, Li Yang, Yin Guo, Wang Mingwei, Meng Fanzheng, Gao Man
机构信息
Department of Pediatric Respiration, Children's Medical Center, The First Hospital of Jilin University, Changchun, China.
Department of Developmental and Behavioral Pediatrics, The First Hospital of Jilin University, Changchun, China.
出版信息
Front Microbiol. 2025 Jul 23;16:1613760. doi: 10.3389/fmicb.2025.1613760. eCollection 2025.
is a leading cause of community-acquired pneumonia (CAP) and upper respiratory tract infections, particularly in children and immunocompromised individuals. The growing global prevalence of macrolide-resistant (MRMP) further emphasizes the urgent need to elucidate its pathogenic mechanisms. Among these, adhesion plays a central role, serving as a prerequisite for colonization and disease progression, and thus warrants detailed investigation. The terminal organelle of mediates both adhesion and gliding motility, facilitating colonization, tissue invasion, and potential systemic spread. In the lung, adhesion triggers cytotoxic effects through the release of hydrogen peroxide (HO) and CARDS toxin (CARDS TX), promotes excessive inflammatory responses, and enables immune evasion via antigenic variation. Extrapulmonary manifestations may also arise either from direct bacterial dissemination or autoimmune responses induced by molecular mimicry between bacterial and host antigens. In addition, recent advances suggest that therapies and vaccines directed at the adhesion mechanism of may offer promising strategies for combating MRMP infections. Although progress has been made, the adhesion-related pathogenesis of , as well as the prospects for therapies and vaccines targeting this mechanism, remains incompletely defined. This review synthesizes current insights into adhesion-mediated mechanisms and highlights emerging therapeutic strategies targeting adhesion, aiming to support more effective treatment and prevention of infection.
是社区获得性肺炎(CAP)和上呼吸道感染的主要病因,尤其是在儿童和免疫功能低下的个体中。全球大环内酯类耐药肺炎支原体(MRMP)的患病率不断上升,进一步凸显了阐明其致病机制的迫切需求。其中,黏附起着核心作用,是定植和疾病进展的先决条件,因此值得详细研究。肺炎支原体的末端细胞器介导黏附和滑行运动,促进定植、组织侵袭和潜在的全身播散。在肺部,黏附通过释放过氧化氢(HO)和CARDS毒素(CARDS TX)触发细胞毒性作用,促进过度的炎症反应,并通过抗原变异实现免疫逃逸。肺外表现也可能源于细菌的直接播散或细菌与宿主抗原之间的分子模拟诱导的自身免疫反应。此外,最近的进展表明,针对肺炎支原体黏附机制的疗法和疫苗可能为对抗MRMP感染提供有前景的策略。尽管已经取得了进展,但肺炎支原体与黏附相关的发病机制以及针对该机制的疗法和疫苗的前景仍未完全明确。本综述综合了目前对黏附介导机制的认识,并强调了针对黏附的新兴治疗策略,旨在支持更有效地治疗和预防肺炎支原体感染。
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