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来自外膜囊泡:重组抗原呈递的平台。

Outer Membrane Vesicles from : A Platform for Recombinant Antigen Presentation.

作者信息

Ginez Luis David, Osorio Aurora, Correal-Medina Víctor, Arenas Thelma, González-Espinosa Claudia, Camarena Laura, Poggio Sebastian

机构信息

Departamento de Biología Molecular y Biotecnologia, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Instituto de Investigaciones Biomédicas, Circuito Mario de la Cueva s/n, Ciudad Universitaria, Ciudad de México 04510, México.

Pharmacobiology Department and Center for Research in Aging, Center for Research and Advanced Studies (Cinvestav), South Campus, Calzada de los Tenorios No. 235, Col. Granjas Coapa, Alcaldía Tlalpan, Ciudad de México 14330, México.

出版信息

ACS Nano. 2025 Jun 10;19(22):20526-20538. doi: 10.1021/acsnano.4c17885. Epub 2025 May 28.

Abstract

Bacterial outer membrane vesicles (OMVs) are an emerging and attractive technology for the generation of vaccines. Their properties as natural adjuvants, size, acellularity, and comparative cost of production favor their use as vaccines. Two major caveats for the use of OMVs as vaccines are their biological safety, since OMVs can induce a severe and even fatal inflammatory response and that they are naturally produced in low amounts. In this study, we show that a strategy to induce the production of OMVs applied to the nonpathogenic bacterium results in a strain with good OMV yields. In comparison with the OMVs derived from K-12, the OMVs from induce a lower inflammatory response in an murine model of acute inflammation and in a human cell assay. Also, only minor signs of pain in mice were observed even at high doses. The OMVs can be efficiently loaded with a recombinant protein and induce antibody production against it with an adjuvant effect, indicating that these OMVs are viable vehicles for the presentation of recombinant antigens. These results support the use of the OMVs obtained from as a safe and effective platform for the development of low-cost vaccines.

摘要

细菌外膜囊泡(OMV)是一种新兴且颇具吸引力的疫苗生产技术。它们作为天然佐剂的特性、大小、无细胞性以及相对较低的生产成本,都有利于将其用作疫苗。将OMV用作疫苗存在两个主要问题,一是其生物安全性,因为OMV可引发严重甚至致命的炎症反应,二是它们天然产量较低。在本研究中,我们表明,一种诱导非致病性细菌产生OMV的策略可得到OMV产量良好的菌株。与源自K - 12的OMV相比,来自[未提及具体细菌名称]的OMV在急性炎症小鼠模型和人体细胞试验中引发的炎症反应较低。此外,即使在高剂量下,在小鼠中也仅观察到轻微的疼痛迹象。[未提及具体细菌名称]的OMV可有效负载重组蛋白,并在具有佐剂效应的情况下诱导针对该重组蛋白的抗体产生,这表明这些OMV是呈递重组抗原的可行载体。这些结果支持将从[未提及具体细菌名称]获得的OMV用作开发低成本疫苗的安全有效平台。

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