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微生物群驱动的天然抗体对登革热传播的影响。

Influence of microbiota-driven natural antibodies on dengue transmission.

机构信息

Anses, INRAE, Ecole Nationale Vétérinaire d'Alfort, UMR Virologie, Laboratoire de Santé Animale, Maisons-Alfort, France.

Universidad Nacional de Asunción, Instituto de Investigaciones en Ciencias de la Salud, San Lorenzo, Paraguay.

出版信息

Front Immunol. 2024 Mar 15;15:1368599. doi: 10.3389/fimmu.2024.1368599. eCollection 2024.

Abstract

Dengue has had a significant global health impact, with a dramatic increase in incidence over the past 50 years, affecting more than 100 countries. The absence of a specific treatment or widely applicable vaccine emphasizes the urgent need for innovative strategies. This perspective reevaluates current evidence supporting the concept of dual protection against the dengue virus (DENV) through natural antibodies (NAbs), particularly anti-α-Gal antibodies induced by the host's gut microbiome (GM). These anti-α-Gal antibodies serve a dual purpose. Firstly, they can directly identify DENV, as mosquito-derived viral particles have been observed to carry α-Gal, thereby providing a safeguard against human infections. Secondly, they possess the potential to impede virus development in the vector by interacting with the vector's microbiome and triggering infection-refractory states. The intricate interplay between human GM and NAbs on one side and DENV and vector microbiome on the other suggests a novel approach, using NAbs to directly target DENV and simultaneously disrupt vector microbiome to decrease pathogen transmission and vector competence, thereby blocking DENV transmission cycles.

摘要

登革热对全球健康造成了重大影响,在过去 50 年中发病率显著增加,影响了 100 多个国家。由于缺乏特定的治疗方法或广泛适用的疫苗,因此迫切需要创新策略。本文重新评估了目前支持通过天然抗体(NAbs)对登革热病毒(DENV)进行双重保护这一概念的证据,特别是由宿主肠道微生物组(GM)诱导的抗-α-Gal 抗体。这些抗-α-Gal 抗体具有双重作用。首先,它们可以直接识别 DENV,因为已经观察到蚊子来源的病毒颗粒携带α-Gal,从而为人类感染提供了保护。其次,它们具有通过与载体微生物组相互作用并引发感染抗性状态来阻止病毒在载体中发展的潜力。人类 GM 和 NAbs 与 DENV 和载体微生物组之间的复杂相互作用表明了一种新方法,即使用 NAbs 直接靶向 DENV,同时破坏载体微生物组以减少病原体传播和载体能力,从而阻断 DENV 传播周期。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3406/10978734/491a27f23532/fimmu-15-1368599-g001.jpg

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